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'''[https://en.wikipedia.org/wiki/Acorus_calamus Acorus calamus L.]''', popularly known as '''Vacha''', is a semi-aquatic perennial herbaceous plant native to temperate and subtropical regions of Asia, Europe, and North America. It is widely revered in [[Ayurveda]] as a powerful medhya (nootropic) and nervine tonic, highly valued for improving intellect, memory, speech, and managing cognitive or neurological disorders.
'''[https://en.wikipedia.org/wiki/Acorus_calamus Acorus calamus L.]''', popularly known as '''Vacha''', is a semi-aquatic perennial herbaceous plant native to temperate and subtropical regions of Asia, Europe, and North America. It is widely revered in [[Ayurveda]] as a powerful medhya (nootropic) and nervine tonic, highly valued for improving intellect, memory, speech, and managing cognitive or neurological disorders. Its rhizome has been used in Ayurveda, Unani, Siddha and Chinese medicine for nervous disorders, colic, cough, fever, inflammation and digestive complaints, and modern studies have examined several of these uses.<ref name="Rajput2014">Rajput SB, Tonge MB, Karuppayil SM. An overview on traditional uses and pharmacological profile of Acorus calamus Linn. (Sweet flag) and other Acorus species. Phytomedicine. 2014;21(3):268–276. doi:10.1016/j.phymed.2013.09.020. PMID: 24200497</ref>


== English name ==  
== English name ==  
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* Out of India: China, Japan, Sri Lanka, Myanmar, Thailand, Indonesia, Malaysia, Philippines, Europe, Germany, Russia, Canada, Kenya, Uganda, Tanzania, Australia, Oceania.
* Out of India: China, Japan, Sri Lanka, Myanmar, Thailand, Indonesia, Malaysia, Philippines, Europe, Germany, Russia, Canada, Kenya, Uganda, Tanzania, Australia, Oceania.


== Phytochemical Composition ==
== Phytoconstituents ==
The therapeutic potential of *Acorus calamus* is derived from its diverse secondary metabolites concentrated in the rhizomes:
=== Major classes of compounds ===
* '''Volatile Essential Oils:''' Rich in beta-asarone, alpha-asarone, and sesquiterpenes.
A comprehensive review reports that about 145 constituents have been isolated and identified from the plant. They belong mainly to the phenylpropanoids (including α-asarone and β-asarone), sesquiterpenoids and monoterpenes, with triterpenoid saponins and other compounds also described.<ref name="Sharma2020">Sharma V, Sharma R, Gautam DS, Kuča K, Nepovimová E, Martins N. Role of Vacha (Acorus calamus Linn.) in neurological and metabolic disorders: evidence from ethnopharmacology, phytochemistry, pharmacology and clinical study. Journal of Clinical Medicine. 2020;9(4):1176. doi:10.3390/jcm9041176</ref>
* '''Phenylpropanoids:''' Eugenol and calamenene derivatives.
* '''Bitters and Glucosides:''' Acoretin and tannins.


== Pharmacological Activities & Therapeutic Efficacy ==
=== Essential oil of the rhizome ===
=== Nootropic and Neuroprotective Effects ===
GC/MS analysis of the rhizome essential oil showed β-asarone (79.54%) and α-asarone (8.47%) as the major constituents. The asarone content varies between plant chemotypes, so these figures apply only to the sample studied.<ref name="Mukherjee2007">Mukherjee PK, Kumar V, Mal M, Houghton PJ. In vitro acetylcholinesterase inhibitory activity of the essential oil from Acorus calamus and its main constituents. Planta Medica. 2007;73(3):283–285. doi:10.1055/s-2007-967114. PMID: 17286241</ref>
* '''Mechanism:''' Active constituents like asarone readily cross the blood-brain barrier, enhancing cognitive functions, neurotransmitter levels (such as acetylcholine), and offering protection against oxidative stress-induced neurodegeneration.
* '''Scientific Evidence:''' Experimental studies demonstrate significant memory enhancement, reversal of cognitive deficits, and reduction of neuroinflammation in animal models of amnesia and dementia.<ref name="Mukherjee2007">{{cite journal |last1=Mukherjee |first1=P. K. |last2=Kumar |first2=V. |last3=Mal |first3=M. |last4=Houghton |first4=P. J. |year=2007 |title=Acetylcholinesterase inhibitors from plants (Review) |journal=Phytomedicine |volume=14 |issue=4 |pages=289–300}}</ref>


=== Anticonvulsant and Sedative Actions ===
== Therapeutic Efficacy: Pharmacological Evidence ==
* '''Mechanism:''' Ethanolic extracts modulate gamma-aminobutyric acid (GABA) receptor systems and suppress central nervous system hyperexcitability, justifying its historical role in managing epilepsy (*apasmara*).
The evidence summarised below comes from animal and in vitro studies. No controlled human clinical trial of ''Acorus calamus'' was verified during the preparation of this monograph.
* '''Scientific Evidence:''' Laboratory evaluations show prolonged latency periods and reduced severity of chemically induced seizures in rodents.<ref name="Jaya2003">{{cite journal |last1=Jayaraman |first1=R. |last2=Anand |first2=S. |last3=Latha |first3=R. |year=2003 |title=Effect of Acorus calamus on seizure models in mice |journal=Journal of Ethnopharmacology |volume=88 |issue=2 |pages=157–161}}</ref>


=== Anti-Inflammatory and Gastroprotective Efficacy ===
=== Nootropic activity (Medhya, Smrti daurbalya) ===
* '''Mechanism:''' The volatile oil fraction exhibits strong inhibition over pro-inflammatory mediators and protects gastric mucosal linings against ulcerogenic stimuli.
In an in vitro Ellman assay, the hydroalcoholic extract, the essential oil and the main constituents of the rhizome inhibited acetylcholinesterase. β-Asarone, the major constituent of the oil, showed the strongest inhibition. This offers a biochemical basis for the traditional use of Vacha to improve memory, although enzyme inhibition in vitro does not by itself prove a memory-enhancing effect in humans.<ref name="Mukherjee2007"/>
* '''Scientific Evidence:''' Research validates its ability to reduce paw edema and decrease gastric ulcer indices in experimental ulcer models.<ref name="Vohora1990">{{cite journal |last1=Vohora |first1=S. B. |last2=Shah |first2=S. A. |last3=Dandiya |first3=P. C. |year=1990 |title=Central nervous system and anti-inflammatory studies on Acorus calamus |journal=Journal of Ethnopharmacology |volume=28 |issue=1 |pages=53–62}}</ref>


== Safety, Toxicity, and Dosage ==
=== Neuroprotective activity ===
* '''Precautions:''' Due to the presence of beta-asarone in certain varieties, high doses or long-term uncontrolled usage of crude wild varieties should be monitored. Pregnant women and young children should use standardized preparations strictly under qualified guidance.
Acorus calamus extract was reported to have a neuroprotective effect against middle cerebral artery occlusion-induced ischaemia in rats.<ref name="Shukla2006">Shukla PK, Khanna VK, Ali MM, Maurya R, Khan MY, Srimal RC. Neuroprotective effect of Acorus calamus against middle cerebral artery occlusion-induced ischaemia in rat. Human & Experimental Toxicology. 2006;25(4):187–194. doi:10.1191/0960327106ht613oa</ref>


=== Central nervous system and sedative activity (Unmada) ===
An ethanol extract of the rhizome was screened for central nervous system activity in mice and rats. It produced a number of actions similar to those of α-asarone, though it differed from it in some respects.<ref name="Vohora1990">Vohora SB, Shah SA, Dandiya PC. Central nervous system studies on an ethanol extract of Acorus calamus rhizomes. Journal of Ethnopharmacology. 1990;28(1):53–62. doi:10.1016/0378-8741(90)90065-2</ref>
=== Anticonvulsant activity (Apasmara) ===
The effect of ''Acorus calamus'' on behavioural, electroencephalographic and antioxidant changes was studied in ferric chloride-induced epileptogenesis in rats. The authors concluded that the plant has potential to be developed as an antiepileptic agent.<ref name="Hazra2007">Hazra R, Ray K, Guha D. Inhibitory role of Acorus calamus in ferric chloride-induced epileptogenesis in rat. Human & Experimental Toxicology. 2007;26(12):947–953.</ref>
=== Anti-inflammatory, analgesic and antipyretic activity ===
In rats, methanol and n-hexane extracts of the rhizome (125, 250 and 500 mg/kg) showed dose-dependent anti-inflammatory, analgesic and antipyretic effects. Paw inflammation in the carrageenan model was significantly reduced.<ref name="Bari2024">Bari MU, et al. Anti-inflammatory, anti-nociceptive, and anti-pyretic activities of Acorus calamus rhizome extracts in animal models. Pakistan Journal of Zoology. 2024. doi:10.17582/journal.pjz/20240506024014</ref>
=== Gastroprotective activity (Shula, Adhmana) ===
Antisecretagogue, antiulcer and cytoprotective properties of ''Acorus calamus'' were reported in rats. This is consistent with its traditional use in colic and abdominal distension, but the data are from animals only.<ref name="Rafatullah1994">Rafatullah S, Tariq M, Mossa JS, Al-Yahya MA, Al-Said MS, Ageel AM. Antisecretagogue, anti-ulcer and cytoprotective properties of Acorus calamus in rats. Fitoterapia. 1994;65(1):19–23.</ref>
== Safety, Toxicity, and Precautions ==
* '''Asarone toxicity:''' The European Medicines Agency's herbal committee stated that α- and β-asarone are genotoxic and cause liver cancer in rodents. It advised caution with herbal products containing asarone, especially those from ''Acorus'' species.<ref name="EMA2005">European Medicines Agency, Committee on Herbal Medicinal Products (HMPC). Public statement on the use of herbal medicinal products containing asarone. EMEA/HMPC/139215/2005. 2005.</ref>
* '''Precautions (inference, not from a cited study):''' High doses or prolonged use of crude, unstandardised preparations should be avoided, since asarone content varies between plant varieties. Pregnant women and young children should use Vacha only under qualified supervision.


== Summary of Therapeutic Profile ==
== Summary of Therapeutic Profile ==
{| class="wikitable sortable" style="text-align: left;"
{| class="wikitable sortable" style="text-align: left;"
|+ Therapeutic Applications of *Acorus calamus*
|+ Therapeutic Applications of ''Acorus calamus'' (preclinical evidence)
! Indication
! Indication !! Experimental finding !! Type of evidence
! Active Biomolecules
|-
! Primary Pharmacological Action
| '''Memory and cognition (Medhya)''' || Acetylcholinesterase inhibition by extract, oil and β-asarone || In vitro
|-
| '''Neurological injury''' || Neuroprotection against induced cerebral ischaemia || Rat model
|-
|-
| '''Cognitive Decline & Memory Loss'''
| '''Epilepsy (Apasmara)''' || Inhibition of ferric chloride-induced epileptogenesis || Rat model
| Alpha-asarone, Beta-asarone
| Nootropic, Acetylcholinesterase inhibition
|-
|-
| '''Epilepsy & Neurological Spasms'''
| '''Pain, inflammation and fever''' || Dose-dependent anti-inflammatory, analgesic and antipyretic effects || Rat models
| Volatile essential oils
| Anticonvulsant, CNS depressant
|-
|-
| '''Digestive Colic & Abdominal Distress'''
| '''Colic, abdominal distress''' || Antiulcer, antisecretory and cytoprotective effects || Rat model
| Sesquiterpenes, Phenylpropanoids
| Carminative, Anti-inflammatory
|}
|}


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<ref name="Tripathi2006">Dr. Indradev Tripathi, Raj Nighantu of Pandit Narahari, ed.2006, Chaukhambha Krishnadas Academy, Varanasi; Pippalyadi Varga – 52.</ref>
<ref name="Tripathi2006">Dr. Indradev Tripathi, Raj Nighantu of Pandit Narahari, ed.2006, Chaukhambha Krishnadas Academy, Varanasi; Pippalyadi Varga – 52.</ref>
<ref name="Chunekar2015">Prof. K.C. Chunekar, Bhavprakasha Nighantu, Reprint 2015, Chaukhambha Vishvabharti, Haritakyadi Varga, verse no. 102, p. 42.</ref>
<ref name="Chunekar2015">Prof. K.C. Chunekar, Bhavprakasha Nighantu, Reprint 2015, Chaukhambha Vishvabharti, Haritakyadi Varga, verse no. 102, p. 42.</ref>
<ref name="Mukherjee2007">{{cite journal |last1=Mukherjee |first1=P. K. |last2=Kumar |first2=V. |last3=Mal |first3=M. |last4=Houghton |first4=P. J. |year=2007 |title=Acetylcholinesterase inhibitors from plants (Review) |journal=Phytomedicine |volume=14 |issue=4 |pages=289–300}}</ref>
<ref name="Rajput2014">Rajput SB, Tonge MB, Karuppayil SM. An overview on traditional uses and pharmacological profile of Acorus calamus Linn. (Sweet flag) and other Acorus species. Phytomedicine. 2014;21(3):268–276. doi:10.1016/j.phymed.2013.09.020. PMID: 24200497</ref>
<ref name="Jaya2003">{{cite journal |last1=Jayaraman |first1=R. |last2=Anand |first2=S. |last3=Latha |first3=R. |year=2003 |title=Effect of Acorus calamus on seizure models in mice |journal=Journal of Ethnopharmacology |volume=88 |issue=2 |pages=157–161}}</ref>
<ref name="Sharma2020">Sharma V, Sharma R, Gautam DS, Kuča K, Nepovimová E, Martins N. Role of Vacha (Acorus calamus Linn.) in neurological and metabolic disorders: evidence from ethnopharmacology, phytochemistry, pharmacology and clinical study. Journal of Clinical Medicine. 2020;9(4):1176. doi:10.3390/jcm9041176</ref>
<ref name="Vohora1990">{{cite journal |last1=Vohora |first1=S. B. |last2=Shah |first2=S. A. |last3=Dandiya |first3=P. C. |year=1990 |title=Central nervous system and anti-inflammatory studies on Acorus calamus |journal=Journal of Ethnopharmacology |volume=28 |issue=1 |pages=53–62}}</ref>
<ref name="Mukherjee2007">Mukherjee PK, Kumar V, Mal M, Houghton PJ. In vitro acetylcholinesterase inhibitory activity of the essential oil from Acorus calamus and its main constituents. Planta Medica. 2007;73(3):283–285. doi:10.1055/s-2007-967114. PMID: 17286241</ref>
<ref name="Shukla2006">Shukla PK, Khanna VK, Ali MM, Maurya R, Khan MY, Srimal RC. Neuroprotective effect of Acorus calamus against middle cerebral artery occlusion-induced ischaemia in rat. Human & Experimental Toxicology. 2006;25(4):187–194. doi:10.1191/0960327106ht613oa</ref>
<ref name="Vohora1990">Vohora SB, Shah SA, Dandiya PC. Central nervous system studies on an ethanol extract of Acorus calamus rhizomes. Journal of Ethnopharmacology. 1990;28(1):53–62. doi:10.1016/0378-8741(90)90065-2</ref>
<ref name="Hazra2007">Hazra R, Ray K, Guha D. Inhibitory role of Acorus calamus in ferric chloride-induced epileptogenesis in rat. Human & Experimental Toxicology. 2007;26(12):947–953.</ref>
<ref name="Bari2024">Bari MU, et al. Anti-inflammatory, anti-nociceptive, and anti-pyretic activities of Acorus calamus rhizome extracts in animal models. Pakistan Journal of Zoology. 2024. doi:10.17582/journal.pjz/20240506024014</ref>
<ref name="Rafatullah1994">Rafatullah S, Tariq M, Mossa JS, Al-Yahya MA, Al-Said MS, Ageel AM. Antisecretagogue, anti-ulcer and cytoprotective properties of Acorus calamus in rats. Fitoterapia. 1994;65(1):19–23.</ref>
<ref name="EMA2005">European Medicines Agency, Committee on Herbal Medicinal Products (HMPC). Public statement on the use of herbal medicinal products containing asarone. EMEA/HMPC/139215/2005. 2005.</ref>
}}
}}


[[Category: Database of herbs and minerals | Herbs]]
[[Category: Database of herbs and minerals | Herbs]]
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