Talk:Ativisha: Difference between revisions
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== Current Availability == | == Current Availability == | ||
Available | Available | ||
* '''In India:''' Jammu & Kashmir, Himachal Pradesh, Uttarakhand | * '''In India:''' Jammu & Kashmir, Himachal Pradesh, Uttarakhand | ||
* '''Out of India:''' Northern Pakistan, Nepal | * '''Out of India:''' Northern Pakistan, Nepal | ||
Conservation status: the species is reported as critically endangered because of over-harvesting.<ref name="Wani2022" /> | Conservation status: the species is reported as critically endangered because of over-harvesting.<ref name="Wani2022" /> | ||
| Line 206: | Line 206: | ||
The pharmacological properties of ''Aconitum heterophyllum'' are primarily attributed to its diterpenoid alkaloids, which are concentrated in the root tubers:<ref name="Mathew2023" /> | The pharmacological properties of ''Aconitum heterophyllum'' are primarily attributed to its diterpenoid alkaloids, which are concentrated in the root tubers:<ref name="Mathew2023" /> | ||
* '''Diterpenoid Alkaloids:''' Atisine,<ref name="Malhotra2014" /><ref name="Jowett1896" /> atidine,<ref name="Jowett1896" /> heteratisine and benzoylheteratisine,<ref name="Jacobs1942" /> and aconitine (used as the HPLC marker compound for standardisation).<ref name="Prasad2014" /> Heterophylline, heterophylloidine, fischimine and aconine derivatives <sup>[citation needed]</sup> | * '''Diterpenoid Alkaloids:''' Atisine,<ref name="Malhotra2014" /><ref name="Jowett1896" /> atidine,<ref name="Jowett1896" /> heteratisine and benzoylheteratisine,<ref name="Jacobs1942" /> and aconitine (used as the HPLC marker compound for standardisation).<ref name="Prasad2014" /> Heterophylline, heterophylloidine, fischimine and aconine derivatives <sup>[citation needed]</sup> | ||
* '''Lactones & Flavonoids:''' Bitter principles and phenolic compounds contributing to digestive and anti-inflammatory actions | * '''Lactones & Flavonoids:''' Bitter principles and phenolic compounds contributing to digestive and anti-inflammatory actions | ||
== Therapeutic Efficacy & Modern Scientific Research == | == Therapeutic Efficacy & Modern Scientific Research == | ||
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== Safety, Toxicity, and Dosage == | == Safety, Toxicity, and Dosage == | ||
* '''Precautions:''' Raw or unpurified roots contain potent aconite-type alkaloids that can be toxic; hence, strict adherence to classical purification (''Shodhana'') processes is mandatory prior to therapeutic usage.<ref name="Shodhana" / | * '''Precautions:''' Raw or unpurified roots contain potent aconite-type alkaloids that can be toxic; hence, strict adherence to classical purification (''Shodhana'') processes is mandatory prior to therapeutic usage.<ref name="Shodhana" /> | ||
* '''Standard Therapeutic Dosage:''' | * '''Standard Therapeutic Dosage:''' | ||
** ''Root Powder (Churna):'' 0.6–2 g daily.<ref name="API" /> | ** ''Root Powder (Churna):'' 0.6–2 g daily.<ref name="API" /> | ||
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{{Reflist|refs= | {{Reflist|refs= | ||
<ref name="API">Anonymous. The Ayurvedic Pharmacopoeia of India. Part I, Vol. I. New Delhi: Government of India, Ministry of Health and Family Welfare; 1986. p. 14.</ref> | <ref name="API">Anonymous. The Ayurvedic Pharmacopoeia of India. Part I, Vol. I. New Delhi: Government of India, Ministry of Health and Family Welfare; 1986. p. 14.</ref> | ||
<ref name="RajaNighantu">Tripathi I, editor. Raj Nighantu of Pandit Narahari, Pippalyadi Varga, verse 136. Varanasi: Chaukhambha Krishnadas Academy. </ref> | <ref name="RajaNighantu">Tripathi I, editor. Raj Nighantu of Pandit Narahari, Pippalyadi Varga, verse 136. Varanasi: Chaukhambha Krishnadas Academy. </ref> | ||
<ref name="Bhavaprakash">Bhavamishra. Bhavaprakash Nighantu, Haritakyadi Varga, verses 186–187. Chunekar KC, editor. Reprint ed. Varanasi: Chaukhambha Bharati Academy; 2015.</ref> | <ref name="Bhavaprakash">Bhavamishra. Bhavaprakash Nighantu, Haritakyadi Varga, verses 186–187. Chunekar KC, editor. Reprint ed. Varanasi: Chaukhambha Bharati Academy; 2015.</ref> | ||
Revision as of 09:10, 6 October 2026
| Section/Chapter | Herb database/Ativisha |
|---|---|
| Botanical name(s) | Aconitum heterophyllum WALL. |
| Family | Ranunculaceae |
| Availability | Available |
| Contributors | Team Dravyaguna |
| Year of publication | 2026 |
| Publisher | Charak Samhita Research, Training and Skill Development Centre |
| DOI | Awaited |
Aconitum heterophyllum WALL., popularly known as Ativisha or Indian Atees, is a perennial herb native to the alpine and sub-alpine regions of the Himalayas.[1] In Ayurveda, it is highly valued as a prominent drug for managing fevers (Jvara), digestive ailments, and pediatric disorders, acting as an Ama-pachana and Kapha-Pitta pacifying medicine.[2][3]
English Name
Indian Atees
Therapeutic Use
Worms (Krimiroga), Fever (Jvara), Cough (Kasa), Vomiting (Chhardi), Amatisara[2]
Other Varieties / Other Botanical names
- Aconitum heterophyllum Wallich
- Aconitum palmatum
- Aconitum kashmiricum
Identification Characters
- Shuklakanda – Root tubers are white in colour.
- Shrungi – Root tubers are horn shaped.[4]
Types
Based on colours of root tubers as per Raja Nighantu:[5]
- Rakta – Red tubers
- Sweta – White tubers
- Krisna – Black tubers
Synonyms in Charak Samhita
- Ativisha
- Shrungi – Root tubers are horn-shaped.
- Virupa
- Pittadivallabha – Efficacious in Pittaja roga.
- Shwetvaca
- Visha
- Maadri – Plant grows in Maadra desh.
Synonyms in Bhavaprakasha Nighantu
- Visha – It assimilates quickly.
- Ativisha
- Vishva
- Shrungi – Root tubers are horn-shaped.
- Prativisha
- Aruna
- Shuklakanda – Root tubers are white in colour.
- Upavisha
- Bhangura
- Dhunavallabha – Root tubers are quickly infested.
Ayurvedic Pharmacological Properties
According to classical Ayurvedic pharmacodynamics (Rasa Panchaka), Ativisha has the following properties:[2]
| Sr. No. | Pharmacological Criteria | Properties (Ayurvedic Attributes) |
|---|---|---|
| 1 | Taste (Rasa) | Bitter (Tikta), Pungent (Katu) |
| 2 | Potency (Veerya) | Hot (Ushna) |
| 3 | Post-digestion Effect (Vipaka) | Pungent (Katu) |
| 4 | Qualities (Guna) | Light (Laghu), Rough (Ruksha) |
| 5 | Dosha Action (Karma) | Reduces Vata, Pitta, and Kapha |
Reference in Charak Samhita and its Actions
Ativisha is prominently documented across multiple therapeutic chapters of the Charaka Samhita:
| Sr. No. | Reference in Charak Samhita | Activity / Formulation / Therapeutic Use |
|---|---|---|
| 1 | Cha.Sa.Sutra Sthana 4/9(3) | Lekhaniya mahakashaya (ingredient of group of herbs for treatment of emaciation) |
| 2 | Cha.Sa.Sutra Sthana 4/9(12) | Arshoghna mahakashay (ingredient of group of herbs for treatment of piles) |
| 3 | Cha.Sa.Sutra Sthana 23/19 | Santarpanajanya vikar chikitsa (management of over-nutrition disease) |
| 4 | Cha.Sa.Sutra Sthana 25/40 | Agrya Sangraha |
| 5 | Cha.Sa.Vimana Sthana 8/139 | Madhur skanda (group of sweet drugs) |
| 6 | Cha.Sa.Vimana Sthana 8/143 | Tiktaskandha (group of bitter drugs) |
| 7 | Cha.Sa.Chikitsa Sthana 3/204 | As an ingredient of Vatsakadi kashaya |
| 8 | Cha.Sa.Chikitsa Sthana 3/219 | As an ingredient of Pippalyadi Ghrita |
| 9 | Cha.Sa.Chikitsa Sthana 6/38 | Trikantakadhya Tail/Ghrit in Vata-kaphaj prameha |
| 10 | Cha.Sa.Chikitsa Sthana 6/42 | Ingredient in Madhvasava |
| 11 | Cha.Sa.Chikitsa Sthana 11/16 | As a diet and drinks in treatment of Kshatakshina |
| 12 | Cha.Sa.Chikitsa Sthana 12/44 | Ingredient in Kshar Gudika |
| 13 | Cha.Sa.Chikitsa Sthana 13/159 | In formulation of Pippalyadi lavana |
| 14 | Cha.Sa.Chikitsa Sthana 14/187 | Used for raktastambhana |
| 15 | Cha.Sa.Chikitsa Sthana 14/230 | As an ingredient of Hriberadi ghrita |
| 16 | Cha.Sa.Chikitsa Sthana 14/236 | As an ingredient of Sunishanak changeri ghrita |
| 17 | Cha.Sa.Chikitsa Sthana 15/98 | Kalka of this drug is used for Aampachan (with usnodaka) |
| 18 | Cha.Sa.Chikitsa Sthana 15/99 | Churna of this drug with combination of vaca, musta, etc. is given in aam and shoola yukta mala |
| 19 | Cha.Sa.Chikitsa Sthana 15/101 | Churna with hingu, abhaya, vaca etc. used in Sama and Vatakapha adhika grahani with kostha shola |
| 20 | Cha.Sa.Chikitsa Sthana 15/105 | Used in Kaphapittaja grahani |
| 21 | Cha.Sa.Chikitsa Sthana 15/129 | As an ingredient of Nagaradhya churna |
| 22 | Cha.Sa.Chikitsa Sthana 15/134, 15/138 | As an ingredient of Kiratadhya churna (Pittaja Grahani chikitsa) |
| 23 | Cha.Sa.Chikitsa Sthana 15/165 | As an ingredient of Madhvarista |
| 24 | Cha.Sa.Chikitsa Sthana 15/173 | As an ingredient of Pipallimuladhya Kshara |
| 25 | Cha.Sa.Chikitsa Sthana 15/186 | Used in preparation of Chaturtha Kshara |
| 26 | Cha.Sa.Chikitsa Sthana 16/61 | As an ingredient of Vishaladi Phanta |
| 27 | Cha.Sa.Chikitsa Sthana 18/115 | As an ingredient of Nagaradi yoga |
| 28 | Cha.Sa.Chikitsa Sthana 19/22 | As an ama pachak dravya |
| 29 | Cha.Sa.Chikitsa Sthana 19/51 | As an ingredient of Ativishadi yoga |
| 30 | Cha.Sa.Chikitsa Sthana 19/105 | As a kwatha dravya |
| 31 | Cha.Sa.Chikitsa Sthana 19/108 | As an ingredient of Rasanjanadi yoga |
| 32 | Cha.Sa.Chikitsa Sthana 26/21 | As an ingredient of Vachadi churna |
| 33 | Cha.Sa.Chikitsa Sthana 26/97 | As an ingredient of Katphaladi kashaya |
| 34 | Cha.Sa.Chikitsa Sthana 26/101 | Used in Hrudshoola |
| 35 | Cha.Sa.Chikitsa Sthana 26/201 | As an ingredient of Katukadi kashaya |
| 36 | Cha.Sa.Chikitsa Sthana 27/35 | As an ingredient of Murvadi Choorna |
| 37 | Cha.Sa.Chikitsa Sthana 27/36 | As an ingredient of Swarnakshiradi Choorna |
| 38 | Cha.Sa.Chikitsa Sthana 28/151 | As an ingredient of Bala taila |
| 39 | Cha.Sa.Chikitsa Sthana 28/168 | As an ingredient of Mulakadhya taila |
Purification (Shodhana)
Ativisha tuberous roots are cut into pieces and kept in Gomutra kvatha for 3 hours and then dried in sunlight.[6]
Dose
- Powder (Churna): 0.6 – 2 g daily.[2]
Important Formulations
As per A.P.I.[2]
- Mahavisagarbha Taila
- Rodhrasava
- Siva gulika
- Laksmi narayana rasa
- Rasnaerandadi kvatha Churna
- Sudarshana Churna
- Panchatikta Guggulu Ghrita
- Bala Chaturbhadra Churna
Current Availability
Available
- In India: Jammu & Kashmir, Himachal Pradesh, Uttarakhand
- Out of India: Northern Pakistan, Nepal
Conservation status: the species is reported as critically endangered because of over-harvesting.[1]
Major Phytoconstituents
The pharmacological properties of Aconitum heterophyllum are primarily attributed to its diterpenoid alkaloids, which are concentrated in the root tubers:[3]
- Diterpenoid Alkaloids: Atisine,[7][8] atidine,[8] heteratisine and benzoylheteratisine,[9] and aconitine (used as the HPLC marker compound for standardisation).[10] Heterophylline, heterophylloidine, fischimine and aconine derivatives [citation needed]
- Lactones & Flavonoids: Bitter principles and phenolic compounds contributing to digestive and anti-inflammatory actions
Therapeutic Efficacy & Modern Scientific Research
Modern pharmacological evaluations and experimental research support some of the traditional therapeutic indications of Aconitum heterophyllum:
1. Anti-diarrheal Action (Atisara)
- Traditional Use: Widely used for Amatisara (diarrhea associated with toxic metabolic wastes) and pediatric gastrointestinal disturbances.[2][3]
- Mechanism & Scientific Evidence: In rat models, an ethanol extract of the roots showed anti-diarrheal activity in castor oil-induced diarrhea and fecal excretion tests. Further tests showed reduced small intestinal transit, reduced intestinal fluid accumulation and inhibition of PGE2-induced enteropooling, indicating antisecretory and antimotility effects that appear to be mediated through the nitric oxide pathway.[10]
2. Antipyretic and Anti-inflammatory Properties (Jvara)
- Traditional Use: Root tubers are commonly used in pediatric medicine for fever management and have been used as an antipyretic and anti-inflammatory agent.[3]
- Mechanism & Scientific Evidence: A network pharmacology and docking study, validated in LPS-stimulated RAW264.7 macrophages, found that a root extract reduced nitric oxide release and iNOS expression, and suppressed EGFR/AKT1 and EGFR/JAK2/STAT3 signalling.[11] These findings are preclinical (in silico and in vitro); direct experimental evidence for the antipyretic effect was not identified in the sources reviewed.
3. Antimicrobial Activity
- Traditional Use: Used to combat infections and normalize bodily humors.[3]
- Mechanism & Scientific Evidence: An aconitine-standardised root extract (0.0833% w/w aconitine) showed antibacterial activity against microbes implicated in diarrhea.[10]
Summary of Therapeutic Profile
| Indication | Active Biomolecules | Primary Pharmacological Action |
|---|---|---|
| Diarrhea & Dysentery (Atisara) | Diterpenoid alkaloids (aconitine used as marker) | Anti-motility, anti-secretory, antibacterial[10] |
| Fever & Inflammation (Jvara) | Diterpenoid alkaloids | Traditional antipyretic use;[3] inhibition of NO release and EGFR/JAK2/STAT3 signalling in vitro[11] |
| Microbial Infections | Aconitine-standardised extract | Antibacterial activity in vitro[10] |
Safety, Toxicity, and Dosage
- Precautions: Raw or unpurified roots contain potent aconite-type alkaloids that can be toxic; hence, strict adherence to classical purification (Shodhana) processes is mandatory prior to therapeutic usage.[6]
- Standard Therapeutic Dosage:
- Root Powder (Churna): 0.6–2 g daily.[2]
References
- ↑ 1.0 1.1 Wani TA, Kaloo ZA, Dangroo NA. Aconitum heterophyllum Wall. ex Royle: a critically endangered medicinal herb with rich potential for use in medicine. J Integr Med. 2022;20(2):104–113. doi:10.1016/j.joim.2021.12.004
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Anonymous. The Ayurvedic Pharmacopoeia of India. Part I, Vol. I. New Delhi: Government of India, Ministry of Health and Family Welfare; 1986. p. 14.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 Mathew A, Chandrashekar KS, Kishore A, Pai V, Aswatha Ram HN, Pemmereddy R. Therapeutic potential of Aconitum heterophyllum: a review on phyto-pharmacological properties. Res J Pharm Technol. 2023;16(1):470–476.
- ↑ 4.0 4.1 Bhavamishra. Bhavaprakash Nighantu, Haritakyadi Varga, verses 186–187. Chunekar KC, editor. Reprint ed. Varanasi: Chaukhambha Bharati Academy; 2015.
- ↑ Tripathi I, editor. Raj Nighantu of Pandit Narahari, Pippalyadi Varga, verse 136. Varanasi: Chaukhambha Krishnadas Academy.
- ↑ 6.0 6.1 Tripathi I, editor. Raj Nighantu of Pandit Narahari, Pippalyadi Varga, verse 137. Varanasi: Chaukhambha Krishnadas Academy.
- ↑ Malhotra N, Kumar V, Sood H, Singh TR, Chauhan RS. Multiple genes of mevalonate and non-mevalonate pathways contribute to high aconites content in an endangered medicinal herb, Aconitum heterophyllum Wall. Phytochemistry. 2014;108:26–34. doi:10.1016/j.phytochem.2014.08.025
- ↑ 8.0 8.1 Jowett HAD. Contributions to our knowledge of the aconite alkaloids. Part XIII. On atisine, the alkaloid of Aconitum heterophyllum. J Chem Soc Trans. 1896;69:1518–1526. doi:10.1039/CT8966901518
- ↑ Jacobs WA, Craig LC. The aconite alkaloids. J Biol Chem. 1942;143(3):589–603. doi:10.1016/S0021-9258(18)72589-1
- ↑ 10.0 10.1 10.2 10.3 10.4 Prasad SK, Jain D, Patel DK, Sahu AN, Hemalatha S. Antisecretory and antimotility activity of Aconitum heterophyllum and its significance in treatment of diarrhea. Indian J Pharmacol. 2014;46(1):82–87. PMC3912813
- ↑ 11.0 11.1 Meng X, Xu X, Shi L, Liu Y, Deng J, Huang X. Network pharmacology combining molecular docking to unveil the anti-inflammatory mechanism of Aconitum heterophyllum. Food Nutr Health. 2025;2:7. doi:10.1007/s44403-025-00016-1
This article is under development ..