Surasa
| Section/Chapter | Herb database/Surasa |
|---|---|
| Botanical name(s) | Ocimum sanctum L.(syn. Ocimum tenuiflorum L.) |
| Family | Lamiaceae |
| Availability | Available |
| Contributors | Team Dravyaguna |
| Year of publication | 2026 |
| Publisher | Charak Samhita Research, Training and Skill Development Centre |
| DOI | Awaited |
Tulasi (Ocimum sanctum L.) is one of the most commonly used and widely available herbs with significant therapeutic efficacy.
Botanical Profile & Phytochemistry
Taxonomic Classification
- Family: Lamiaceae
- Species: Ocimum sanctum L.(syn. Ocimum tenuiflorum L.)
- Common Names: Tulsi, Holy Basil, Surasa
Therapeutic uses
Aruchi,Swasa(dyspnea), kasa(cough), krumiroga(worm), kustha(skin disease), pratishyaya(rhinitis), parshwashoola(flank pain)[1]
Synonyms in Charak Samhita
Surasa, Tulsi, Kutherak, Phaninjhak, Arjaka(Tulsi bheda)
Synonyms in bhavprakasa nighantu
Gramya(Common plant grown in all villages), Sulabha(can be seen every where), bahumanjari(tulasi has got many spikes), Apetaraxasi(tulasi brings back normalcy by alleviating many disease), gauri , bhutagni, devadundubhi(the spikes of tulasi resemble a trumpet)[2]
Varieties
Bhavaprakasa nighantu
Mentioned 2 types[3]
- Sweta tulasi
- Krishna tulasi
Ayurvedic pharmacological properties
| Sr.no. | Pharmacological criteria | Properties |
| 1 | Taste (rasa) | Pungent (katu), Bitter (tikta) |
| 2 | Potency (veerya) | Hot (ushna) |
| 3 | Post digestion effect (vipaka) | Pungent (katu) |
| 4 | Qualities (guna) | Light (laghu), Rough (ruksha) |
| 5 | Actions (karma) | Pacify Kapha and Vata |
| 6 | Extra ordinary effect (prabhava) | Destroys microbes/germs (krimighna) |
Reference in Charak Samhita and its actions
| Sr.no. | Reference in Charak Samhita | Activity |
| 1 | Cha.Sa.Sutra Sthana 2/4 | Sirovirechana (Errhine therapy) |
| 2 | Cha.Sa.Sutra Sthana 4/9(37) | Shwasahara mahakashaya |
| 3 | Cha.Sa.Nidana Sthana 2/4 | Nidana of Raktapitta |
| 4 | Cha.Sa.Vimana Sthana 6/17 | Abhyantar Krimi Chikitsa |
| 5 | Cha.Sa.Vimana Sthana 6/21 | Abhyantar Krimi Chikitsa |
| 6 | Cha.Sa.Chikitsa Sthana 3/267 | As an ingredient of Agurvadi taila |
| 7 | Cha.Sa.Chikitsa Sthana 5/70 | Ingredient of Hingusauvarchaladya ghrita |
| 8 | Cha.Sa.Chikitsa Sthana 7/112 | Ingredient in Kanakakshiri Taila |
| 9 | Cha.Sa.Chikitsa Sthana 8/101 | Ingredient in Avaleha |
Dose
- 2-3 gm of the drug in powder form[4]
Important formulation
As per A.P.I.[5]
- Manasamitra vataka
- Tribhuvana kirti
- Mukta Panchamruta rasa
- Mahajwarankusa rasa
Current availability
Available India- All over india
Current researches
Primary Phytoconstituents
- Phenylpropanoids: Eugenol (up to 70–80% in volatile oil), methyleugenol, rosmarinic acid.
- Triterpenes: Ursolic acid, oleanolic acid.
- Flavonoids: Apigenin, luteolin, orientin, vicenin.
- Sesquiterpenes: β-caryophyllene.
Pharmacological Mechanism & Therapeutic Efficacy
Adaptogenic and Antistress Activity
- Mechanisms: Regulates the hypothalamic-pituitary-adrenal (HPA) axis, suppresses acute elevation of plasma cortisol, and modulates central neurotransmitters (dopamine and serotonin).
- Evidence: Clinical trials using standardized extracts demonstrate reductions in self-reported stress, cognitive fatigue, and stress-induced sleep disturbances.[6]
Immunomodulatory and Anti-inflammatory Effects
- Mechanisms: Downregulates pro-inflammatory cytokines (TNF-α, IL-6, IL-1β) through inhibition of the NF-κB pathway. Ursolic acid and eugenol selectively inhibit cyclooxygenase-2 (COX-2) activity.
- Evidence: Human clinical studies show significant increases in natural killer (NK) cells and T-helper (CD4+) lymphocytes following leaf extract administration.[6]
Antidiabetic and Metabolic Regulation
- Mechanisms: Enhances insulin secretion from pancreatic β-cells, increases peripheral glucose uptake, and inhibits hepatic gluconeogenesis.
- Evidence: Clinical studies show a statistically significant reduction in fasting blood glucose (FBG) and postprandial blood glucose (PPBG) in patients with type 2 diabetes mellitus.[6]
Antimicrobial and Biofilm Inhibition
- Mechanisms: Disrupts bacterial plasma membrane integrity and inhibits quorum sensing due to high eugenol content.
- Evidence: Broad-spectrum antibacterial action demonstrated against Streptococcus mutans, Staphylococcus aureus, and Pseudomonas aeruginosa.[6]
Key Bioactive Compounds
| Chemical Class | Major Compound | Biological Activity | Primary Mechanism |
|---|---|---|---|
| Phenolic/Monoterpene | Eugenol | Anti-inflammatory, Analgesic | COX-2 inhibition, free-radical scavenging |
| Pentacyclic Triterpene | Ursolic Acid | Anti-inflammatory, Antitumor | Downregulation of NF-κB, induction of apoptosis |
| Flavonoid Glycoside | Orientin / Vicenin | Radioprotective, Antioxidant | Lipid peroxidation suppression, DNA repair acceleration |
| Polyphenol | Rosmarinic Acid | Immunomodulatory, Antiviral | Complement activation inhibition, ROS neutralization |
Clinical Evidence Summary
| Target Condition | Study Type | Dosage & Duration | Key Clinical Outcome | Reference |
|---|---|---|---|---|
| Generalized Anxiety / Stress | Double-Blind RCT | 300–1200 mg/day extract (6–8 weeks) | Decreased stress scores, improved attention and sleep | Cohen (2014)[6] |
| Type 2 Diabetes Mellitus | Crossover Clinical Trial | 2.5 g leaf powder daily (4 weeks) | Significant reduction in FBG (17.6%) and PPBG (7.3%) | Cohen (2014)[6] |
| Immune Response Modulation | Open-label Phase I Trial | 300 mg ethanolic extract daily (4 weeks) | Significant elevation in IFN-γ, IL-4, CD4+ count | Cohen (2014)[6] |
| Metabolic Syndrome / Lipids | Double-Blind RCT | 1000 mg/day extract (8 weeks) | Reduced total cholesterol, LDL-C, and triglycerides | Cohen (2014)[6] |
Toxicology and Safety
- Acute Toxicity: Preclinical studies indicate an LD50 > 4000 mg/kg body weight for aqueous and ethanolic leaf extracts, establishing a wide therapeutic index.[6]
- Adverse Effects: Highly tolerated in clinical trials. Mild transient gastrointestinal distress reported rarely.
- Drug Interactions: May exert additive effects when co-administered with hypoglycemic agents or anticoagulants (due to mild antiplatelet activity). Use caution in patients on antiplatelet therapy.
References
- ↑ Anonymous. The Ayurvedic Pharmacopoeia of India. Department of Ayush, Ministry of Health and Family welfare, Govt. of India, New Delhi, Part I. 1986; Volume 2 :73
- ↑ Pro. Krushnachandra Chunekar, Bhavaprakash Nighantu. Reprint Edition 2020, Chaukhambha Bharati Academy, pushpa varga, verse no.-62
- ↑ Pro. Krushnachandra Chunekar, Bhavaprakash Nighantu. Reprint Edition 2020, Chaukhambha Bharati Academy, pushpa varga, verse no.-63
- ↑ Anonymous. The Ayurvedic Pharmacopoeia of India. Department of Ayush, Ministry of Health and Family welfare, Govt. of India, New Delhi, Part I. 1986; Volume 2 :73
- ↑ Anonymous. The Ayurvedic Pharmacopoeia of India. Department of Ayush, Ministry of Health and Family welfare, Govt. of India, New Delhi, Part I. 1986; Volume 2 :73
- ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.8 Cohen, Marc Maurice (2014). "Tulsi - Ocimum sanctum: A herb for all reasons". Journal of Ayurveda and Integrative Medicine. 5 (4): 251–259. PMC 4296439 . PMID 25624696. doi:10.4103/0975-9476.146554.