A Systemic Review of Tulsi (Ocimum tenuiflorum or Ocimum sanctum): Phytoconstituents, Ethnobotanical and Pharmacological Profile
Pooja*, Anil Kumar
Dept. of Biotechnology, GOVT. V.Y.T. PG. Auto. College, Durg (C.G.)
*Corresponding Author E-mail: poojakumari3491@gmail.com
ABSTRACT:
Ocimum tenuiflorum Linn. is an Ayurvedic herb commonly regarded as Tusli or Holy Basil. The plant has a long traditional medicinal history. In India Tulsi is worshipped by Hindus and is abundantly found in all regions. Each part of a plant like stems, roots, seeds, leaves, flowers, and fruits have their own curative properties and functions reported by many researchers. The varieties of active chemical constituents; terpenoids, phenols, flavonoids, phenylpropanoids, fatty acid derivatives, essential oil, fixed oil, and steroids are extracted from the Ocimum tenuiflorum plant and are determined of great therapeutic activities. The therapeutic actions of Tulsi compounds recreate their remedial attention and in the standardization of their medicinal results. Eugenol, Oleanolic Acid, Linalool, Ursolic Acid, Beta-Caryophyllene, Rosemarinic Acid, Estragole, Carvacrol, Methyl Cinnamate are the major compounds which are leads to various actions against diseases. This review article summarizes researchers validated various pharmacological actions of these active chemical constituents that have great potential against, antidiabetic, antioxidant, anti- inflammatory, antimicrobial, antiviral (especially against Covid-19/Coronavirus, helpful in the current scenario of “pandemic”), cardioprotective, antihypertensive, and other activities as well. This will be useful for developing new active principles and therapeutics or new life-saving drugs by researchers, practitioners, and students who were implicated in the field of ethnopharmacology.
KEYWORDS: Ocimum tenuiflorum, Ocimum sanctum, Tulsi, Pharmacological activities, Chemical constituents.
1. INTRODUCTION:
Globally various plants have been used for the treatment of several diseases or their healing goals. In the Indian system of medicine various kinds of Ocimum tenuiflorum were preferred and apt as pharmaceutical constructions 1. According to Ayurveda Ocimum tenuiflorum is known as: "Mother medicine of nature”, "The incomparable one", "Queen of Herbs", "Elixir of Life", etc. 2. O. tenuiflorum is commonly called “Tulsi” in Hindi and “Holy Basil” in English 3. Tulsi is an important sign of Hindu intellectual traditions.
Among all of the other herbs, Tulsi is highly used in Ayurveda 4. To cure various modern-day illnesses Tulsi is the best Ayurvedic wisdom tonic for the mind and body. It plays a major role in the traditional “Ayurveda” and “Unani” systems 5.
Ocimum tenuiflorum L. is a species or variety of the plant family Lamiaceae. Due to the high number of remedial potential, it has contributed in the area of science from ancient till now in modern practices 3.Tulsi mainly grows in the tropics and warm regions throughout the world. In India, Tulsi originated from North Central India and distributed and cultivated all over the country 6. Rama Tulsi (most common one, broad bright leaves and slightly sweet), Shyama Tulsi (least common one and have purplish leave), and Vana Tulsi (wild Tulsi and grows in the forests) are the 3 morphotypes, cultivated in India 1, 7. Various active constituents are present in Tulsi, some of them show a high rate of affectivity and fast relief, while others take a certain time for recovery and healing from diseases 8. It belongs to the genus Ocimum, the largest genera of the Lamiaceae family consisting more than 150 species 9, 10. It act as an adaptogen, maintains the different body processes, and is helpful for stress adaptation and detoxification 11, 12. The varieties of species of Ocimum genus were cultivated in different areas throughout the globe for their known remedial and medicinal properties 13. Various important species of Ocimum are cultivated globally for their beneficial uses and phytochemical constituents (Table.1).
Tulsi is a straight, highly branched, erected, and fragrant shrub. An aromatic plant, height 30 to 60cm. Leaves are oval, colour- simple green or purple, margin- slightly dented or toothed, and blade length is 5cm 14. The flowers are purplish and small and hairy stem. Plant have small fruit and reddish-yellow seeds. The taste is acrid and bitter 15, 16.
Binomial Name:
Ocimum tenuiflorum L. or Ocimum sanctum L.
Taxonomy
Kingdom - Plantae Subkingdom - Tracheobionta Superdivision - Spermatophyta Division - Magnoliophyta Class - Magnoliopsida Subclass - Asteridae
Order – Lamiales Family – Lamiaceae Genus – Ocimum Linn
Species – Ocimum tenuiflorum Linn. or Ocimum sanctum Linn.
Table.1: The Description about Important Species of Ocimum.
S. No. |
Species |
Geographical Distribution |
Biochemical Constituents |
General, Traditional, and Modern Uses |
Ref. |
1. |
Ocimum tenuiflorum L. or Ocimum sanctum L. |
India, Andaman And Nicobar Islands, Nepal, Bangladesh, China, USA, Kenya, Nigeria, |
Eugenol, Methyl Eugenol, apigenin-7-O- glucuronide, carvacrol, circimaritin, caryophyllen, cirsilineol, isothymusin, pinene, molludistin, rosameric acid, orientin, vicenin, Ursolic acid, luteolin, sesquiterpine hydrocarbon, luteolin-7- Oglucuronide, apigenin, camphor |
Antistress, antimicrobial, antioxidant, antilarval, antiviral and antifungal. Antiasthmatic, anti- inflammatory, analgesic, hypotensive and hypoglycemic activity. Treatment for snakebite and scorpion-stings. Radiation protection. To treat cough, cold, sore throat, fever, headache, dysentery, ulcer and skin diseases. Treatment against HIV. Anti-dibetic, anticancer, hepatoprotective and hypolipidimic activity. |
[1] [2] [11] [14] [16] [17] [18] [19] [20] [21] [22] [23] [62] [37] [40] [63] |
2. |
Ocimum americanum |
Tropical Africa, South East Asia, Indian Subcontinent, Sri Lanka, China, Madagascar, Burma, Thailand, |
α-pinene, Isoborneol, Linalool, Limonene, linalool oxide, Humulene, α bisabolene, Camphor, Anethole, Eugenol, Z-β-ocimene, |
To treat conjunctivitis, Fever, Malaria, headache, Indigestion, dysentery, toothache, and migraine. Antioxidant and enzyme inhibitory effects. Antifungal and antibacterial. Insect and pest control. |
[17] [24] [25] [26] [27] [28] [29] [30] [31] [38] |
|
|
Malesia and Indonesia |
t-hydrate-sabinene, Bicyclogermacrene, β-caryophyllene, Carvacrol, p-menthadiene, 3-O-Caffeoylquinic acid, Vitexin |
Preservative for corpses. Flavoring and fragrance to foods. To treat hypothermia, skin allergy, cancer, and ulcer. |
|
3. |
Ocimum basilicum |
Bangladesh, Colombia, Bulgaria, Mali, Guinea, Nigeria, Eastern Morocco. |
Eugenol, Methyl Chavicol, Methyl eugenol, Geraniol, Linalool, Geranial, Cadinene, methyl cinnamate |
Food and oral care products. Antilarval, Antiviral, Antimicrobial, insecticidal, antiparasitic, antioxidant, immunomodulatory, anti- inflammatory, hepatoprotective, anti- osteoporotic activities. Decrease plasma lipid content. For treating nausea, flatulence, and dysentery. First aid treatment for wasp stings and snakebites. Inhibitory activity against HIV-1 reverse transcriptase. |
[10] [17] [32] [33] [34] [35] [36] [37] [38] |
4. |
Ocimum kilimandscharicum |
Kenya. Rwanda, Athens, Nigeria, Sudan, Ghana, and India. |
d-camphor, Camphene, Myrcene, d-α- pinene, ß-pinene, Epi-α-cadinol, d-limonene, Linalool, terpinolene, Bornyl acetate, Eugenol Germacerene B, ß-caryophyllene, γ-muurolene and unidentified sesquiterpenes and sesquiterpenes of alcohols |
Antioxidant, antimalarial, antimicrobial, antiseptic, allergenic, pesticidal, antitumor, spasmogenic and antiviral activity. Useful in cold and cough, abdominal pains, measles, diarrhea, bronchitis, foul ulcers and wounds, opthalmopathy and vitiated conditions of ‘vata’. CNS activities like: neurotoxic, antineuralgic, CNS stimulant, tranquilizer, Anti-alzhemerian, sedative. |
[39] [40] [41] [42] [43] [44] [45] [46] [47] [48] [49] |
5. |
Ocimum gratissimum |
India, Nigeria, New Zealand, Autralia, South Amaerica, The Caribbean, South East Asia, and Africa. |
Eugenol, thymol, citral, geraniol and linalool, eugenol |
Antifungal, antiviral and antioxidant. Antinociceptive activity. For treatment of rheumatism, paralysis, epilepsy, sunstroke, influenza, Gonorrhea, highfever, diarrhea, and mental illness |
[39] [50] [51] [52] [53] [54] [55] [67] |
6. |
Ocimum micranthum |
Central and South America, West Indies. |
1,8-cineol, eugenol elemene isomers, linalool, ß-caryophyllen |
Treatment of colds, fever, stomach disturbances, and dysentery. Antimicrobial. To treat epilepsy, nervous trouble, influenza, earaches. |
[56] [57] [58] [59] [60] |
7. |
Ocimum canum |
India, Rwanda, Israel, Zimbabwe, Somali, Nigeria, USA, Central Africa, |
Eugenol,linalool, Terpineol, Linalyl acetate, camphor, methyl chavicol, Geraniol, Nerol, Geranial, Terpinen-4-ol, Methyl cinnamate, 1.8- cineole. |
Treat conjunctivitis, malaria and headache Insecticidal and antibacterial and antifungal activity. |
[61] [62] [63] [64] [65] [66] [67] [68] [69] |
Traditionally, Tulsi was consumed as an herbal tea or in the form of dried powder or direct fresh leaves or with Honey/Ghee 17. The dried leaves of Tulsi are used as an insect repellent for stored grains21. From ancient times in “Ayurveda” and tribal medicine, Tulsi is being used as a remedy for the treatment of common cold, cough, wound, fatigue, headache, flu, fever, sore throat, and skin diseases or allergies62. Leaves crushed in goat’s urine and mixed with coconut oil is used against skin allergies. According to “Charaka Samhita” it is used for treatment against snake bites (whole plant used) and scorpion sting (leaf paste) 17. Leaves pounded with onion bulbs are used for cold, cough, and headache70. It helps in the maintenance of body glucose level (powdered leave with honey), reduces breathing problems, and increases digestion of foods. Dried leaves with ghee are useful in dysentery, colic, and piles treatment. Leaves paste with black pepper is used to treat diarrhea, and fever. Flower’s juice in combination with honey, ginger and onion leaves juice is used for the treatment of bronchitis 71. In Thailand to treat vomiting, the leaf or entire plant is used 59. The plant leaves are also used for the purification of drinking water, for memory sharpening, good for nerves, to treat ulcers and mouth infections60, 61.
The plant shows various therapeutic and medicinal properties, due to the presence of chemical constituents or phyto components. In species, O. tenuiflorum various kinds of phytoconstituents and their activities were reported 18 (Table.2). The essential oil extracted from O. tenuiflorum
L. consists high amount of Eugenol (near about 70 %), other constituents are 11% of Beta- Elemene, 8% of Beta-Caryophyllene, and 2% Germacrene 1. The leaves of the plant consist of volatile oil (0.7%) made up of eugenol and methyl eugenol in 71% and 20% respectively. It consist carvacrol, sesquiterpene and caryophyllene hydrocarbon also62. Phenolic compounds isolated
from the concentrate of fresh leaves and stem of Ocimum sanctum show antioxidants properties 64. The isolated phenolic compounds are isothymusin, circimaritin, cirsilineol, apigenin, and rosameric acid, and Eugenol (in high quantity) 16. Orientin and Vicenin are the 2 types of flavonoids extracted from aqueous leaf extract. Others like; Ursolic acid, orientin, luteolin, apigenin-7-O-glucuronide, molludistin and luteolin-7-Oglucuronide, are also extracted from the extract of Tulsi leaveas 21. This species of Ocimum also contains a variety of sesquiterpenes and monoterpenes; bornyl acetate, β elemene, neral, and pinenes (both α and β), camphene, sitosterol, cholesterol, campesterol, and stigmasterol 22. Five types of fatty acids – stearic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid are present in O. sanctum 23. Tulsi is a excellent source of vitamin C, beta carotene, and Ca2+ions. Tannins, camphor, other flavonoids like; luteolin, orientin, vicenin, and triterpene; urolic acid, with Zn, Mn, and Na ions found in plant extract 21,23.
The major chemical constituents of O. tenuiflorum Linn which are possessed in high amounts and leads to several remedial activities are; Eugenol (C10H12O2), Oleanolic Acid (C30H48O3), Linalool (C10H18O), Ursolic Acid (C30H48O3), Beta-Caryophyllene (C15H24), Rosemarinic Acid (C18H16O8), Estragole (C10H12O), Carvacrol (C10H14O), Methyl Cinnamate (C10H10O2) (Fig.1) 11.
Fig.1: Structure of major chemical constituents of Ocimum tenuiflorum.
Worldwide various scientific experiments of Ocimum tenuiflorum have been designed to evaluate the pharmacological actions, their after-effects or side effects, and their therapeutic uses against various diseases. Based on various experimental and clinical investigations on Ocimum tenuiflorum, the following pharmacological activities or therapeutic properties were reported.
This activity was reported by many researchers 3, 71. Flavonoids have antioxidant properties and their role in membrane protection was observed 71. Antioxidant activity of the flavonoids (orientin and vicenin) in vivo resulted in a significant reduction in the radiation-induced lipid peroxidation in mouse liver 20, 72. Tulsi extract has significantly scavenged high reactive free radicals 12. The Tulsi extract from leaves and stem have phenolic compounds and showed great antioxidant actions. The rosemarinic acid, isothymusin, cirsilineol, cirsimaritin, eugenol, and apigenin are the name of extracted phenolic commixture 29.
When the Tulsi extract is administered orally it results in decrease blood sugar in both, glucose- fed hyperglycemic and streptozotocin-induced diabetic rats 73. By modulating the intracellular Ca+2 channel the extract of Tulsi stimulates the physiological pathway for the secretion of insulin via stimulating pancreatic β-cell 74. In clinical studies, placebo-controlled (a randomized and cross-over single-blind trial) – indicates a decrease in blood glucose (fasting-17.6% and postprandial-7.3%) level, quite similarly showed in urine glucose level. Tulsi also have aldose reductase activity, it helps to overcome side effects of diabetes (cataract, retinopathy, etc.)12 75. Hydro-alcoholic extract of Tulsi found significant against streptozotocin (at dose level- 250 mg/kg body weight) and nicotinamide (at dose level-500mg/kg body weight) in comparison with glibenclamide 76. Ethanol extract of Tulsi reduces hyperglycemia in alloxan diabetic rats 74.
The leaf extracts and essential oil from Tulsi were reported as having antimicrobial activity 3. Tulsi is effective against various strains of bacteria and fungi. Alcoholic extract of Tulsi is found effective against Vibrio cholera 77. The aq. Extract is effective against Gram-positive and Gram- negative bacterial strains 3. Linalool shows the most prevalent against candidiasis, caused by Candida species. It decreases the growth and metabolism rate of candida by inhibiting proton pumps 78. Fixed oil (mainly linolenic acid and ß-caryophyllene) showed growth inhibition against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, and Bacillus pumilus. It is also resistant to Neisseria gonorrhea strains 10, 3, 11.
The chemopreventive activity of Tulsi extract was detected through the consecration of hepatic/extrahepatic GST in mice. In Tulsi extract supplemented mice, raised levels of deflated GSH were found in liver, lungs, and stomach tissues 79. The seed oil of Tulsi in high concentrations showed significant anti-proliferative and chemopreventive exercise in mice 40. The quiescent chemopreventive activity of seed oil imputed its antioxidant and cancer prevention activity 80.
The anticancer property of Tulsi has been experimentally proven and referred by many researchers [14, 59]. The alcoholic extract of Tulsi leaves was highly affected carcinogen metabolizing compounds or enzymes such as cytochrome P450, cytochrome b5, glutathione S-transferase (GST), and aryl hydrocarbon hydroxylase, which are highly important for cancer-causing agents and mutagens [81]. In human fibrosarcoma cell cultures, phytoconstituents are reported to have anticancer activity, here anticancer activity is accounted as morphological changes on culture; shrunken cytoplasm, condensed nuclei, contracted cells, and dense core [82]. Tulsi significantly diminished the incidence of benzo (a) pyrene instigated neoplasia of forestomach of mice and 3'- methyl-4-dimethylaminoazo-benzene persuaded hepatomas in rodents [83]. The beer of Tulsi leaves was significantly reported as an inhibitory effect on artificially induced skin papillomas in mice [84]. The initiation of papillomagenesis induced by 7, 12-dimethyl benz (a) anthracene (DMBA, a polycyclic aromatic hydrocarbon), when topical treatment of Tulsi extract was performed, reduces the tumor occurrence capacity and papilloma formation in mice [79]. The significantly high reduction of GSH substance and GST exercises are other applications of topical use of extracts [22]. The Ocimum tenuiflorum fresh leaves, glue, or paste were taken orally can prevent the early occasions of DMBA induced buccal pouch carcinogenesis [85]. The chemical carcinogenesis events were suppressed by inactivating the metabolic process of carcinogen, Tulsi
leaf extract activity 86. The anticancer property of Tulsi was detected in Swiss albino mice bearing Ehrlich ascites carcinoma (EAC) and tumor S 180 87.
The Tulsi phyto-constituents radioprotectivity impact, firstly observed in - 1995 72. The flavonoids extracted from the leaves of Tulsi; orientin and vicenin indicate better radioprotective influence as contrasted with synthetic or artificial radioprotectors. They have indicated significant protection towards human lymphocytes against clastogenic action of radiation at mediocre, inoffensive concentrations 88. The combination of Ocimum tenuiflorum extract with WR-2721 (synthetic) shows the high protective activity of bone marrow cell and reduces harmfulness and toxicity of WR-2721 at higher dose 89.
The methanol leaf extracts of Tulsi are effective in altering the dimethylnitrosamine implicated hepatotoxicity 86. The hydro-ethanolic extract of Tulsi leaves orally administrated at 200mg/kg gave protection against liver injury persuaded by paracetamol, in male Wistar albino rats 90. Ocimum tenuiflorum cold water extract was adequate against carbon tetrachloride invaded liver injury in albino rats 91.
Leaf extracts of Tulsi in benzene and petroleum ether solvent were expressed high antifertility activity in female rats, 80% and 60% respectively 92. Similarly, the benzene extracts highly responsible for diminishing sperm tally, testis weight, and motility of sperm reported in male rodents 93. The Ursolic acid; one of the major component of Tulsi, possess antifertility effect. This effect is related to an anti-estrogenic mechanism that is responsible for lacking or arresting male rat spermatogenesis 92, 93.
The fixed oil of Tulsi (O. tenuiflorum) showed antipyretic activity 93. It was assessed by tests on rodents by inducing pyrexia through typhoid-paratyphoid A/B vaccine. The IP (intraperitoneal) administration of oil significantly reduced the febrile reaction indicating its antipyretic properties.
The fixed oil also has an inhibitory effect on prostaglandin. The antipyretic activity of oil at a dose of 3ml/kg was similar to ibuprofen and aspirin 94.
An adaptogenic activity depends upon the immune stimulant capacity of Tulsi [11, 12]. The whole plant alcoholic extract increased the physical perseverance (survival time) of swimming mice, forestalled stress prompted ulcers and milk actuated leukocytosis respectively in rats and mice, indicating acceptance of vaguely increased 95.
Intra-peritoneal administration of O. sanctum fixed oil evoked high antiulcer activity against Indomethacin, Reserpine, Serotonin, alcohol (50% C2H5OH), Histamine, Aspirin, and stress instigated ulcers in rodents 94. Lipoxygenase inhibition, antisecretory, and histamine antagonistic effects present in fixed oil significant amount possessed antiulcer activity 96.
The fixed oil of Tulsi (dose-3ml/kg, intra-peritoneal) demonstrated that prolongation in blood clotting time and the whole reaction was comparable with aspirin (dose-100mg/kg). The impact produced by Tulsi oil on platelets, expected as anti-aggregator 97.
Ocimum sanctum seed extract in hydro-alcohol showed great efficiency for cardioprotection. Tulsi plants have varieties of bioactive constituents, including quercetin, diosgenin, carotinized, isoflavones, catechin, and sulforaphane have been reported as an enhancer of cardioprotection, hence lacking the risk of cardiac abnormalities 98. Effect of hydroalcoholic extract of Tulsi investigated against myocardial infarction (MI) rats, MI induced by subcutaneously administered isoproterenol (ISO). The level of glutathione, superoxide dismutase, and LDH reduced significantly in rats. It also inhibits lipid peroxidation. Tulsi at the dose of 50mg/kg shows the maximum rate of cardioprotective 99.
The Ocimum tenuiflorum Linn were prevented transient cerebral ischemia (a brief stroke-like attack) and long-term cerebral hypoperfusion (causing cellular oedema, gliosis and perivascular inflammatory invade) 100. The Tulsi fixed oil contains; linoleic and linolenic acids (essential fatty acids), it produces PGE-1 and PGE-3 (prostaglandins- atrial pressure regulator) and inhibits PGE-2 (it increases blood pressure and hypertension) formation 20, 100.
The chemical constituents of Tulsi show antiviral activity. Majorly ursolic acid and eugenol demonstrated antiviral activity including influenza 34.
Various studies were suggested that chlorophyll derivatives reported against enveloped viruses including HIV. Ocimum sanctum chlorophyll derivative “Pheophytin-a” has a potential anti-HIV agent attacking HIV-1 protease. “Phy-a” was reported as an inhibitor of HIV replication 101.
Methanolic extract of Tulsi plant exhibit antiviral properties toward dengue virus 1 (DENV 1) through inhibition of viral replication and cytopathic (host cell- structural changes) formation 102, 103.
O. sanctum (Tulsi), phytoconstituents are reported as Anti-covid-19 activity. Out of 46 active phyto-constituents of Tulsi, only three components; Vicenin (flavonoid), Isorientin 4′-O-glucoside 2″-O-p-hydroxybenzoate (a flavon), and Ursolic acid (a natural triterpene compound) were showed positive response against covid-19 virus. In comparison with to built-in ligand N3 for SARS-CoV- 2 Mpro, these compounds gave significant binding affinity. Apart from this vicenin reported as highest binding energy (8.97 kcal/mol), it interacts with C and π-donor hydrogen bonding with Glu 166, Thr 190, Gln 189 and Pro 168 residues along with Met 165 (π-sulfur bonding), and Cys 145 (allyl interaction). The isorientin interacts with Arg 40, Arg 105, Arg 188 residues (a positive charged H-bond), and Tyr 54 residue with hydrophobic interaction with binding energy 8.55 kcal/mol. The ursolic acid, binding energy- 8.52 kcal/mol binds with Leu 272, Leu 287, and Tyr 239 residues (alkyl and π-alkyl interaction) and with Leu 271 (carbon-hydrogen bonding) residues. They have reduced the capacity of translation of viral proteins 104.
Analgesic activity of Tulsi was found in experimental models. It was highly reactive against acetic acid introduced writhing model in rodents (dose-dependent manner). The inhibitory effect of oil was demonstrated due to joint inhibitory effects of histamine, acetylcholine, and prostaglandins 105.
The new leaves refined extract of O. sanctum demonstrated alteration in the humoral resistant reaction in pale-skinned rodents. The extract adjusts, cell intervened insusceptible receptiveness and GABergic pathways arbitrate immunomodulatory effects 106. A randomized double-blind control trial is conducted in healthy volunteers to assess the immunomodulatory action of Tulsi. The results are shown in elevated amounts of interferon-γ and interleukin-4 including T-helper cells and Natural killer cells 107. A significant enhancement in anti-sheep RBC antibody titer and low % histamine revealed from peritoneal mast cells of stimulated rats (humoral immune response), and the decrease in thickness and % inhibition of leukocyte migration (LMI) of Tulsi seed oil (3 ml/kg, IP) 108. The oral dose of aqueous extract of Tulsi accelerates the production of WBC, RBC hemoglobin and it also enhances the manufacture of antibodies without stirring the biochemical parameters 109.
The aqueous extract of Tulsi leaves that delayed the cataractogenesis is a preliminary model of cataract (naphthalene cataract in rabbits- 1g/kg and galactosemic cataract in rodents-30%). The higher dose is very much effective 110.
Wide varieties of chemical constituents were reported as antiarthritic activity. In Tulsi essential oil (ursolic acid, apigenin, luteolin) from leaves and flower extract showed antiarthritic activity 111. It was screened by Singh et al. in 1996 using against formaldehyde-inducted arthritis, Freund’s adjuvant arthritis, and turpentine oil-induced joint edema in rats 112.
The whole dried plant or extract of Leaves (aqueous} and entire plant {alcoholic} of Tulsi enhanced the amnesic effect of scopolamine (0.4mg/kg) and maturing initiated memory shortfalls in mice. This greatly abolishes the acetylcholine esterase .and down dormancy (SDL) restraint. Thus, Tulsi is used for the treatment of Alzheimer’s, and dementia (psychological disorders) 113, 114.
Table 2: Chemical Constituents of Ocimum tenuiflorum and Their Activities.
Bio-Chemical Constituents |
Source |
Characteristics |
Uses/Activity |
Ref. |
Eugenol |
Whole plant |
Phenylpropane |
Antimicrobial, Antilarvacidal, Antidiabetic |
[1] [29] [34] [62] |
Camphor |
Leaves |
Terpenoid |
Antimicrobial, Antiviral |
[21] [114] |
Ursolic acid |
Leaves |
Pentacyclic triterpenoid |
Anti-fertility, Antiarthiritis, Anti-covid-19 |
[104] [111] |
Linalool |
Whole plant |
Terpene alcohol |
Antilaravcidal, Antimalarial, Antimicrobial |
[78] [114] |
Methylchavicol |
Leaves |
Phenylpropane |
Free radical scavenging |
[29] |
Methyl cinnamate |
Whole plant |
Methyl ester of cinnamate |
Food additives |
[3] [114] |
Methyleugenol |
Leaves |
Phenylpropane |
Antimicrobial |
[13] [62] |
Caryophyellene |
Leaves |
Sesquiterpene (Natural, bicyclic) |
Antimicrobial, Antilarval, Anticataract |
[3] [10] [62] [114] |
Isothymusin |
Aerial part |
Flavonoid |
Anticancer |
[29] |
Orientin |
Leaves |
Glycosidic flavonoid |
Anticancer, radioprotective, lipid peroxidation |
[72] [88] |
Vicenin |
Leaves |
Glycosidic flavonoid |
Anticancer, radioprotective, Anti-covid-19 |
[104] [114] |
Rosemarinic acid |
Leaves |
Phenolic |
Anticancer, Hepatoprotective, Antioxidant |
[29] [50] |
Estragole, |
Whole plant |
Phenylpropane |
Antimicrobial |
[3] |
Pheophytin-a |
Leaves |
Chlorophyll derivative |
Anti-HIV activity |
[101] |
Luteolin |
Leaves, flowers |
Flavonoids |
Antiarthritic |
[111] |
Cirisilineol |
Leaves |
Phenolic or biphenyl |
Antioxidant |
[29] |
Linolenic acid |
Seeds |
Omega-3 fatty acid |
Antimicrobial, Antiviral, Antihypertensive |
[11] [100] |
Oleanolic Acid |
Leaves, Roots |
Pentacyclic triterpenoid |
Hepatoprotective, Antioxidant, Antistress |
[3] [86] |
Quercetin |
Leaves |
Flavonoid |
Antioxidant, Cardioprotective |
[98] |
Apigenin |
Flowers, Leaves |
Flavone glycosides |
Anti-inflammatory, Antioxidant, Antiarthritic |
[29] [111] |
Isorientin |
Leaves |
Flavone |
Anti covid-19 activity |
[104] |
Catechin |
Whole plant |
Phenol |
Cardioprotective |
[98] |
Isoflavones |
Seeds |
Polyphenolic |
Antioxidant |
[31] |
Sulforaphane |
Leaves |
Isothiocyanate |
Cardioprotective, Antioxidant |
[98] |
Disogenin |
Roots |
Phytosteroid saponin |
Antioxidant, hypoglycemia, Anti-inflammatory, Antiproliferative |
[114] [115] |
Although, various studies have been done for evaluating the usefulness of, Tulsi in various ailments and clinical conditions there remains a gap between the discovery and development of effective drugs with this preliminary knowledge. The present article on Ocimum sanctum or Ocimum tenuiflorum or Tulsi describes the review on previous medicinal prominences, phytoconstituents, and former pharmacological performed works. Extensensive research needs to be done in the identification and isolation of the bioactive molecules that confer the medicinal properties to this plant. The isolation of such bioactive molecules will help in better understanding the molecular interaction of these molecules at the cellular level and help in the development of drugs with the highest efficacy.
1. Khurana, P. A Review On Medicinal Uses of Ocimum Tenuiflorum Linn (TULSI).
2. Singh, N., Hoette, Y., and Miller, D. R. (2002). Tulsi: The mother medicine of nature. International Institute of Herbal Medicine.
3. Pandey, G., and Madhuri, S. (2010). Pharmacological activities of Ocimum sanctum (tulsi): a review. Int J Pharm Sci Rev Res, 5(1), 61-66.
4. Cohen M. M. (2014). Tulsi - Ocimum sanctum: A herb for all reasons. Journal of Ayurveda and integrative medicine, 5(4), 251–259.
5. Kumar, K. P., Bhowmik, D., Tripathi, K. K., and Chandira, M. (2010). Traditional Indian Herbal Plants Tulsi and Its Medicinal Importance. Research Journal of Pharmacognosy and Phytochemistry, 2(2), 93-101.
6. Pattanayak P, Behera P, Das D, Panda SK. Ocimum sanctum Linn. A reservoir plant for therapeutic applications: An overview. Pharmacogn Rev. 2010 Jan;4(7):95-105.
7. Singh, E., Sharma, S., Dwivedi, J., and Sharma, S. (2012). Diversified potentials of Ocimum sanctum Linn (tulsi): an exhaustive survey. Journal of Natural Product and Plant Resources, 2(1), 39-48.
8. Bhooshitha, A. N., Ghosh, A. R., Chandan, H. M., Nandhini, H. S., Pramod, B. R., and Krishna, K. L. (2020). Review On Nutritional, Medicinal and CNS Activities of Tulsi (Ocimum. Sanctum). Journal of Pharmaceutical Sciences and Research, 12(3), 420-426.
9. Evans, W. C. (1996). Phenols and phenolic glycosides. Trease and Evans Pharmacognosy, 14th ed. Noida: Gopsons Papers Limited, 218.
10. Sajjadi, S. E. (2006). Analysis of the essential oils of two cultivated basil (Ocimum basilicum L.) from Iran. DARU Journal of Pharmaceutical Sciences, 14(3), 128-130.
11. Kumar, P. K., Kumar, M. R., Kavitha, K., Singh, J., and Khan, R. (2012). Pharmacological actions of Ocimum sanctum–review article. International Journal of Advances in Pharmacy, Biology and Chemistry, 1(3), 2277-4688.
12. Wangcharoen, W., and Morasuk, W. (2007). Antioxidant capacity and phenolic content of holy basil. Songklanakarin J Sci Technol, 29(5), 1407-1415.
13. Atal, C. K., and Kapur, B. M. (1982). Cultivation and utilization of medicinal plants. Jammu- Tawi: Regional Research Laboratory, Council of Scientific and Industrial Research.
14. Gupta, P. A Review on Medicinal Uses of Ocimum Tenuiflorum LINN (TULSI).
15. Prajapati, N. D., Purohit, S. S., Sharma, A. K., and Kumar, T. (2003). A handbook of medicinal plants: A complete source book. In A handbook of medicinal plants: a complete source book (pp. 554-554).
16. Gupta, S. K., Prakash, J., and Srivastava, S. (2002). Validation of traditional claim of Tulsi, Ocimum sanctum Linn.as a medicinal plant.
17. Tewari, D., Sah, A. N., Pandey, H. K., Meena, H. S., Meena, R., Ramaswamy, R. S., ... and Murthy, P. H. (2012). A review on phytoconstituents of Ocimum (Tulsi). International Journal of Ayurvedic Medicine, 3(1), 1-9.
18. Chauhan, N. S. (1999). Medicinal and aromatic plants of Himachal Pradesh. Indus publishing.
19. Shah, C. S., and Qadry, J. S. A Textbook of Pharmacognosy. 1998. Back to cited text, (32), 216.
20. Yanpallewar, S. U., Rai, S., Kumar, M., and Acharya, S. B. (2004). Evaluation of antioxidant and neuroprotective effect of Ocimum sanctum on transient cerebral ischemia and long- term cerebral hypoperfusion. Pharmacology Biochemistry and Behavior, 79(1), 155-164.
21. Nair, A. R., Gunasegaran, R., and Joshi, B. S. (1982). Chemical investigation of certain south Indian plants. Indian Journal of Chemistry Section B-Organic Chemistry Including MEDICINAL Chemistry, 21(10), 979-980.
22. Patani, A. (2002). Indian Herbal Pharmacopoeia. Mumbai: Indian Drug Manufactures Association.
23. Singh, S., Majumdar, D. K., and Rehan, H. M. S. (1996). Evaluation of anti-inflammatory potential of fixed oil of Ocimum sanctum (Holybasil) and its possible mechanism of action. Journal of Ethnopharmacology, 54(1), 19-26.
24. Rucinque, D. S., Ferreira, P. F., Leme, P. R. P., Lapa-Guimarães, J., and Viegas, E. M. M. (2021). Ocimum americanum and Lippia alba essential oils as anaesthetics for Nile tilapia: Induction, recovery of apparent unconsciousness and sensory analysis of fillets. Aquaculture, 531, 735902.
25. Zengin, G., Ferrante, C., Gnapi, D. E., Sinan, K. I., Orlando, G., Recinella, L., ... and Menghini, L. (2019). Comprehensive approaches on the chemical constituents and pharmacological properties of flowers and leaves of American basil (Ocimum americanum L). Food Research International, 125, 108610.
26. Sen, S. K., and Behera, L. M. (2008). Ethnomedicinal plants used by the tribals of Bargarh district to cure diarrhoea and dysentery.
27. Shah, A., and Rahim, S. (2017). Ethnomedicinal uses of plants for the treatment of malaria in Soon Valley, Khushab, Pakistan. Journal of ethnopharmacology, 200, 84-106.
28. Selvi, M. T., Thirugnanasampandan, R., and Sundarammal, S. (2015). Antioxidant and cytotoxic activities of essential oil of Ocimum canum Sims. from India. Journal of Saudi Chemical Society, 19(1), 97-100.
29. Adomako-Bonsu, A. G., Chan, S. L., Pratten, M., and Fry, J. R. (2017). Antioxidant activity of rosmarinic acid and its principal metabolites in chemical and cellular systems: Importance of physico-chemical characteristics. Toxicology in vitro, 40, 248-255.
30. Oyedemi, S. O., Oyedemi, B. O., Coopoosamy, R. M., Prieto, J. M., Stapleton, P., and Gibbons, S. (2017). Antibacterial and norfloxacin potentiation activities of Ocimum americanum L. against methicillin resistant Staphylococcus aureus. South African Journal of Botany, 109, 308-314.
31. Pandey, R., Chandra, P., Kumar, B., Dutt, B., and Sharma, K. R. (2016). A rapid and highly sensitive method for simultaneous determination of bioactive constituents in leaf extracts of six Ocimum species using ultra high performance liquid chromatography-hybrid linear ion trap triple quadrupole mass spectrometry. Analytical Methods, 8(2), 333-341.
32. Dhama, K., Sharun, K., Gugjoo, M. B., Tiwari, R., Alagawany, M., Iqbal Yatoo, M., ... and Farag, M. R. (2021). A Comprehensive Review on Chemical Profile and Pharmacological Activities of Ocimum basilicum. Food Reviews International, 1-29.
33. Surburg, H., and Panten, J. Common Fragrance and Flavor Materials.
34. Chiang, L. C., Ng, L. T., Cheng, P. W., Chiang, W., and Lin, C. C. (2005). Antiviral activities of extracts and selected pure constituents of Ocimum basilicum. Clinical and Experimental Pharmacology and Physiology, 32(10), 811-816.
35. Hussain, A. I., Anwar, F., Sherazi, S. T. H., and Przybylski, R. (2008). Chemical composition, antioxidant and antimicrobial activities of basil (Ocimum basilicum) essential oils depends on seasonal variations. Food chemistry, 108(3), 986-995.
36. Baytop, T. (1984). Therapy with Medicinal Plants in Turkey (Past and Present) No: 3255. Istanbul: Publications of the Istanbul University, 359.
37. Mondello, L., Zappia, G., Cotroneo, A., Bonaccorsi, I., Chowdhury, J. U., Yusuf, M., and Dugo, G. (2002). Studies on the essential oil‐bearing plants of Bangladesh. Part VIII. Composition of some Ocimum oils O. basilicum L. var. purpurascens; O. sanctum L. green; O. sanctum L. purple; O. americanum L., citral type; O. americanum L., camphor type. Flavour and fragrance journal, 17(5), 335-340.
38. Viña, A., and Murillo, E. (2003). Essential oil composition from twelve varieties of basil (Ocimum spp) grown in Colombia. Journal of the Brazilian chemical society, 14(5), 744- 749.
39. Kéita, S. M., Vincent, C., Schmit, J. P., and Bélanger, A. (2000). Essential oil composition of Ocimum basilicum L., O. gratissimum L. and O. suave L. in the Republic of Guinea. Flavour and fragrance journal, 15(5), 339-341.
40. Charles, D. J., and Simon, J. E. (1992). Essential oil constituents of Ocimum kilimandscharicum Guerke. Journal of essential oil Research, 4(2), 125-128.
41. Barker, C., Dunn, H. C., and Hilditch, T. P. (1950). African drying oils. V. Some Nigerian and Sudanese drying oils. Journal of the Society of Chemical Industry, 69(3), 71-75.
42. Sastri, B. N. (1962). The Wealth of India. A Dictionary of Indian Raw Materials and Industrial Products. Raw Materials, Vol. 6: LM. The Wealth of India. A Dictionary of Indian Raw Materials and Industrial Products. Raw Materials, Vol. 6: LM.
43. Soni, N., Gill, D., Sagar, B. S., Raheja, S., and Agrawal, S. (2012). Ocimum kilimandscharicum: A systematic review. Journal of Drug Delivery and Therapeutics, 2(3).
44. Ntezurubanza, L. J. J. C., Scheffer, J. J. C., Looman, A., and Svendsen, A. B. (1984). Composition of Essential Oil of Ocimum kilimandscharicum Grown in Rwanda1. Planta medica, 50(05), 385-388.
45. Prakash, P. A. G. N., and Gupta, N. (2005). Therapeutic uses of Ocimum sanctum Linn (Tulsi) with a note on eugenol and its pharmacological actions: a short review. Indian journal of physiology and pharmacology, 49(2), 125.
46. Nadkarni, K., and Nadkarni, A. K. (1976). Indian Materia Medica, Popular Prakashan Pvt. Ltd., Bombay, 1, 799.
47. Warrier, P. K., Nambiar, V. P. K., Ramankutty, C., and Indian Medi-cinal Plants, A. (1995). A compendium of 500 species. Indian Medicinal Plants. Orient Longman Publisher, 4, 157-168.
48. Kweka, E. J., Mosha, F. W., Lowassa, A., Mahande, A. M., Mahande, M. J., Massenga, C. P., ... and Temu, E. A. (2008). Longitudinal evaluation of Ocimum and other plants effects on the feeding behavioral response of mosquitoes (Diptera: Culicidae) in the field in Tanzania. Parasites and Vectors, 1(1), 1-8.
49. Singh, P., Kalunke, R. M., Shukla, A., Tzfadia, O., Thulasiram, H. V., and Giri, A. P. (2020). Biosynthesis and tissue-specific partitioning of camphor and eugenol in Ocimum kilimandscharicum. Phytochemistry, 177, 112451.
50. Awogbindin, I. O., Tade, O. G., Metibemu, S. D., Olorunsogo, O. O., and Farombi, E. O. (2014). Assessment of flavonoid content, free radical scavenging and hepatoprotective activities of Ocimum gratissimum and Spondias mombin in rats treated with dimethylnitrosamine. Arch Basic Appl Med, 2, 45-54.
51. Dubey, N. K., Tiwari, T. N., Mandin, D., Andriamboavonjy, H., and Chaumont, J. P. (2000). Antifungal properties of Ocimum gratissimum essential oil (ethyl cinnamate chemotype). Fitoterapia, 71(5), 567-569.
52. Akinmoladun, A. C., Ibukun, E. O., Afor, E., Obuotor, E. M., and Farombi, E. O. (2007). Phytochemical constituent and antioxidant activity of extract from the leaves of Ocimum gratissimum. Scientific Research and Essays, 2(5), 163-166.
53. Dhawan, B. N., Patnaik, G. K., Rastogi, R. P., Singh, K. K., and Tandon, J. S. (1977). Screening of Indian plants for biological activity: part VI.
54. Rabelo, M., Souza, E. P., Soares, P. M. G., Miranda, A. V., Matos, F. J. A., and Criddle, D. N. (2003). Antinociceptive properties of the essential oil of Ocimum gratissimum L. (Labiatae) in mice. Brazilian Journal of Medical and Biological Research, 36(4), 521- 524.
55. Edeoga, H. O., Omosun, G., and Uche, L. C. (2006). Chemical composition of Hyptis suaveolens and Ocimum gratissimum hybrids from Nigeria. African Journal of Biotechnology, 5(10).
56. Charles, D. J., Simon, J. E., and Wood, K. V. (1990). Essential oil constituents of Ocimum micranthum Willd. Journal of agricultural and food chemistry, 38(1), 120-122.
57. Sacchetti, G., Medici, A., Maietti, S., Radice, M., Muzzoli, M., Manfredini, S., ... and Bruni, R. (2004). Composition and functional properties of the essential oil of Amazonian basil, Ocimum micranthum Willd., Labiatae in comparison with commercial essential oils. Journal of Agricultural and Food Chemistry, 52(11), 3486-3491.
58. Vieira, P. R., de Morais, S. M., Bezerra, F. H., Ferreira, P. A. T., Oliveira, Í. R., and Silva, M. G. V. (2014). Chemical composition and antifungal activity of essential oils from Ocimum species. Industrial Crops and Products, 55, 267-271.
59. de Vasconcelos Silva, M. G., Matos, F. J. A., Machado, M. I. L., and de Oliveira Silva, F. (2004). Essential Oil Composition of the Leaves of Ocimum micranthum Willd. Journal of Essential Oil Research, 16(3), 189-190.
60. Caamal-Herrera, I. O., Carrillo-Cocom, L. M., Escalante-Réndiz, D. Y., Aráiz-Hernández, D., and Azamar-Barrios, J. A. (2018). Antimicrobial and antiproliferative activity of essential oil, aqueous and ethanolic extracts of Ocimum micranthum Willd leaves. BMC complementary and alternative medicine, 18(1), 1-9.
61. Sen, P. (1993). Therapeutic potentials of Tulsi: from experience to facts. Drugs News and Views, 1(2), 15-21.
62. Hasan, S. B., and Deo, P. S. (1994). Ocimum sanctum seeds for mosquito control. International pest control, 36(1), 20-21.
63. Mukherjee, P. K., Maiti, K., Mukherjee, K., and Houghton, P. J. (2006). Leads from Indian medicinal plants with hypoglycemic potentials. Journal of ethnopharmacology, 106(1), 1- 28.
64. Jena, J., Ranjan, R., Ranjan, P., and Sarangi, M. K. (2012). A study on natural anticancer plants. Int J Pharmaceut Chem Sci, 1(1), 365-8.
65. Nadkarni, K. M. (1996). [Indian materia medica]; Dr. KM Nadkarni's Indian materia medica: with Ayurvedic, Unani-Tibbi, Siddha, allopathic, homeopathic, naturopathic and home remedies, appendices and indexes. 1 (Vol. 1). Popular Prakashan.
66. Ngassoum, M. B., Ousmaila, H., Ngamo, L. T., Maponmetsem, P. M., Jirovetz, L., and Buchbauer, G. (2004). Aroma compounds of essential oils of two varieties of the spice plant Ocimum canum Sims from northern Cameroon. Journal of Food Composition and Analysis, 17(2), 197-204.
67. Martins, A. P., Salgueiro, L. R., Vila, R., Tomi, F., Cañigueral, S., Casanova, J., ... and Adzet, T. (1999). Composition of the essential oils of Ocimum canum, O. gratissimum and O. minimum. Planta medica, 65(02), 187-189.
68. Ravid, U., Putievsky, E., Katzir, I., and Lewinsohn, E. (1997). Enantiomeric composition of linalol in the essential oils of Ocimum species and in commercial basil oils. Flavour and fragrance journal, 12(4), 293-2
69. Euloge, S. A., Kouton, S., Dahouenon-Ahoussi, E., Sohounhloue, D. C. K., and Soumanou, M. M. (2012). Antifungal activity of Ocimum canum essential oil against toxinogenic fungi isolated from peanut seeds in post-harvest in Benin. International Research Journal of Biological Sciences, 1(7), 20-26.
70. Dewangan, A., Sahu, B. P., and Meher, B. (2020). Review on Pharmacological Potential of Ocimum sanctum L. Advanced Journal of Bioactive Molecules, 17-24.
71. Madhuri, S., and Govind, P. (2010). Effect of ProImmu, a herbal drug on estrogen caused uterine and ovarian cytotoxicity. Biomed, 5(1), 57-62.
72. Saija, A., Scalese, M., Lanza, M., Marzullo, D., Bonina, F., and Castelli, F. (1995). Flavonoids as antioxidant agents: importance of their interaction with biomembranes. Free Radical Biology and Medicine, 19(4), 481-486.
73. Chattopadhyay, R. R. (1993). Hypoglycemic effect of Ocimum sanctum leaf extract in normal and streptozotocin diabetic rats. Indian journal of experimental biology, 31(11), 891-893.
74. Hannan, J. M. A., Marenah, L., Ali, L., Rokeya, B., Flatt, P. R., and Abdel-Wahab, Y. H. A. (2006). Ocimum sanctum leaf extracts stimulate insulin secretion from perfused pancreas, isolated islets and clonal pancreatic β-cells. Journal of Endocrinology, 189(1), 127-136.
75. Nagarajan, S., Jain, H. C., and Aulakh, G. S. (1987). Indigenous plants used in the control of diabetes. Publication and Information Directorate, CSIR, New Delhi, 586.
76. Parasuraman, S., Balamurugan, S., Christapher, P. V., Petchi, R. R., Yeng, W. Y., Sujithra, J., and Vijaya, C. (2015). Evaluation of antidiabetic and antihyperlipidemic effects of hydroalcoholic extract of leaves of Ocimum tenuiflorum (Lamiaceae) and prediction of biological activity of its phytoconstituents. Pharmacognosy research, 7(2), 156.
77. Geeta Vasudevan, D. M., Kedlaya, R., Deepa, S., and Ballal, M. (2001). Activity of Ocimum sanctum (the traditional Indian medicinal plant) against the enteric pathogens. Ind. J. Med. Sci, 55(8), 434-438.
78. Khan, A., Ahmad, A., Manzoor, N., and Khan, L. A. (2010). Antifungal activities of Ocimum sanctum essential oil and its lead molecules. Natural Product Communications, 5(2), 1934578X1000500235.
79. Prashar, R., and Kumar, A. (1995). Chemopreventive action of Ocimum sanctum on 2, 12- dimethylbenz (a) anthracene DMBA-induced papillomagnesis in the skin of mice. International journal of pharmacognosy: a journal of crude drug research.
80. Prakash, J., and Gupta, S. K. (2000). Chemopreventive activity of Ocimum sanctum seed oil. Journal of ethnopharmacology, 72(1-2), 29-34.
81. Uma Devi, P., Ganasoundari, A., Vrinda, B., Srinivasan, K. K., and Unnikrishnan, M. K. (2000). Radiation protection by the ocimum flavonoids orientin and vicenin: mechanisms of action. Radiation research, 154(4), 455-460.
82. Karthikeyan, K., Gunasekaran, P., Ramamurthy, N., and Govindasamy, S. (1999). Anticancer activity of Ocimum sanctum. Pharmaceutical biology, 37(4), 285-290.
83. Aruna, K., and Sivaramakrishnan, V. M. (1992). Anticarcinogenic effects of some Indian plant products. Food and Chemical Toxicology, 30(11), 953-956.
84. Devi, P. U. (2001). Radioprotective, anticarcinogenic and antioxidant properties of the Indian holy basil, Ocimum sanctum (Tulasi).
85. Karthikeyan, K., Ravichandran, P., and Govindasamy, S. (1999). Chemopreventive effect of Ocimum sanctum on DMBA-induced hamster buccal pouch carcinogenesis. Oral oncology, 35(1), 112-119.
86. Prashar, R., Kumar, A., Hewer, A., Cole, K. J., Davis, W., and Phillips, D. H. (1998). Inhibition by an extract of Ocimum sanctum of DNA-binding activity of 7, 12- dimethylbenz [a] anthracene in rat hepatocytes in vitro. Cancer letters, 128(2), 155-160.
87. Somkuwar, A. P. (2003). Studies on anticancer effects of Ocimum sanctum and Withania somnifera on experimentally induced cancer in mice (Doctoral dissertation, Jawaharlal Nehru Krishi Viswavidyalaya; Jabalpur).
88. Devi, P. U., and Ganasoundari, A. (1995). Radioprotective effect of leaf extract of Indian medicinal plant Ocimum sanctum. Indian Journal of Experimental Biology, 33(3), 205- 208.
89. Ganasoundari, A., Devi, P. U., and Rao, B. S. S. (1998). Enhancement of bone marrow radioprotection and reduction of WR-2721 toxicity by Ocimum sanctum. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 397(2), 303-312.
90. Chattopadhyay, R. R., Sarkar, S. K., Ganguly, S., Medda, C., and Basu, T. K. (1992). Hepatoprotective activity of Ocimum Sanctum leaf extract against Paracetamol included Hepatic damage in rats.
91. Seethalakshmi, B., Narasappa, A. P., and Kenchaveerappa, S. (1982). Protective effect of Ocimum sanctum in experimental liver injury in albino rats. Indian J Pharmacol, 14, 63.
92. Ahmed, M., Ahamed, R. N., Aladakatti, R. H., and Ghosesawar, M. G. (2002). Reversible anti-fertility effect of benzene extract of Ocimum sanctum leaves on sperm parameters and fructose content in rats. Journal of Basic and Clinical Physiology and Pharmacology, 13(1), 51-60.
93. Singh, S., Taneja, M., and Majumdar, D. K. (2007). Biological activities of Ocimum sanctum L. fixed oil—An overview.
94. Srinivas, N., Sali, K., and Bajoria, A. A. (2016). Therapeutic aspects of Tulsi unraveled: A review. Journal of Indian Academy of oral medicine and radiology, 28(1), 17.
95. Bhargava, K. P., and Singh, N. (1981). Anti-stress activity of Ocimum sanctum Linn.
96. Singh, S., and Majumdar, D. K. (1999). Evaluation of the gastric antiulcer activity of fixed oil of Ocimum sanctum (Holy Basil). Journal of ethnopharmacology, 65(1), 13-19.
97. Singh, S., Rehan, H. M. S., and Majumdar, D. K. (2001). Effect of Ocimum sanctum fixed oil on blood pressure, blood clotting time and pentobarbitone-induced sleeping time. Journal of ethnopharmacology, 78(2-3), 139-143.
98. Shah, S. M. A., Akram, M., Riaz, M., Munir, N., and Rasool, G. (2019). Cardioprotective potential of plant-derived molecules: a scientific and medicinal approach. Dose- response, 17(2), 1559325819852243.
99. Sharma, M., Kishore, K., Gupta, S. K., Joshi, S., and Arya, D. S. (2001). Cardioprotective potential of Ocimum sanctum in isoproterenol induced myocardial infarction in rats. Molecular and cellular biochemistry, 225(1), 75-83.
100.Kelm, M. A., Nair, M. G., Strasburg, G. M., and DeWitt, D. L. (2000). Antioxidant and cyclooxygenase inhibitory phenolic compounds from Ocimum sanctum Linn. Phytomedicine, 7(1), 7-13.
101.Kapewangolo, P., Kandawa-Schulz, M., and Meyer, D. (2017). Anti-HIV activity of Ocimum labiatum extract and isolated pheophytin-a. Molecules, 22(11), 1763.
102.Ling, A. P., Khoo, B. F., Seah, C. H., Foo, K. Y., Cheah, R. K., Chye, S. M., and Koh, R. Y. (2014, August). Inhibitory activities of methanol extracts of Andrographis paniculata and Ocimum sanctum against dengue-1 virus. In International Conference on Biological Environmental and Food Engineering: Bali, Indonesia (pp. 4-5).
103.Hemalika, D. V. D., and Chandrika, U. G. Anti-dengue effects of medicinal plants: A review.
104.Shree P, Mishra P, Selvaraj C, Singh SK, Chaube R, Garg N, Tripathi YB. Targeting COVID-19 (SARS-CoV-2) main protease through active phytochemicals of ayurvedic medicinal plants - Withania somnifera (Ashwagandha), Tinospora cordifolia (Giloy) and Ocimum sanctum (Tulsi) - a molecular docking study. J Biomol Struct Dyn. 2020 Aug 27:1-14. doi: 10.1080/07391102.2020.1810778. Epub ahead of print. PMID: 32851919; PMCID: PMC7484581.
105.Singh, S., and Majumdar, D. K. (1995). Analgesic activity of Ocimum sanctum and its possible mechanism of action. International journal of Pharmacognosy, 33(3), 188-192.
106.Mediratta, P. K., Sharma, K. K., and Singh, S. (2002). Evaluation of immunomodulatory potential of Ocimum sanctum seed oil and its possible mechanism of action. Journal of Ethnopharmacology, 80(1), 15-20.
107.Mondal, S., Varma, S., Bamola, V. D., Naik, S. N., Mirdha, B. R., Padhi, M. M., ... and Mahapatra, S. C. (2011). Double-blinded randomized controlled trial for immunomodulatory effects of Tulsi (Ocimum sanctum Linn.) leaf extract on healthy volunteers. Journal of ethnopharmacology, 136(3), 452-456.
108.Mediratta PK, Dewan V, Bhattacharya SK, Gupta VS, Maiti PC, Sen P. Effect of Ocimum sanctum Linn. on humoral immune responses. Indian J Med Res. 1988 Apr;87:384-6. PMID: 3169894.
109.Jeba, C. R., Vaidyanathan, R., and Rameshkumar, G. (2011). Immunomodulatory activity of aqueous extract of Ocimum sanctum in rat. Int J Pharm Biomed Res, 2(1), 33- 8.
110.Sharma, P., Kulshreshtha, S., and Sharma, A. L. (1998). Anti-cataract activity of Ocimum sanctum on experimental cataract. Indian journal of pharmacology, 30(1), 16.
111.Kadian, R., and Parle, M. (2012). Therapeutic potential and phytopharmacology of tulsi. International Journal of Pharmacy and Life Sciences, 3(7).
112.Singh, S., and Majumdar, D. K. (1996). Effect of fixed oil of Ocimum sanctum against experimentally induced arthritis and joint edema in laboratory animals. International Journal of Pharmacognosy, 34(3), 218-222.
113.Kadian, R., and Parle, M. (2012). Therapeutic potential and phytopharmacology of tulsi. International Journal of Pharmacy and Life Sciences, 3(7).
114.Upadhyay, R. K. (2017). Tulsi: A holy plant with high medicinal and therapeutic value. International Journal of Green Pharmacy (IJGP), 11(01).
115.Singh, M., Hamid, A. A., Maurya, A. K., Prakash, O., Khan, F., Kumar, A., ... and Bawankule, D. U. (2014). Synthesis of diosgenin analogues as potential anti-inflammatory agents. The Journal of steroid biochemistry and molecular biology, 143, 323-333.
Received on 05.04.2023 Modified on 19.04.2023
Accepted on 27.04.2023 ©A&V Publications All right reserved
Res. J. Pharmacognosy and Phytochem. 2023; 15(2):179-188.
DOI: 10.52711/0975-4385.2023.00028