Article by Justin L Scharton, Independent Researcher
Article written on February 10, 2025
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Hyperhidrosis (excessive sweating)
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Sweating Under Control: Receptors, Pharmacology, and Terpenes for Hyperhidrosis
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Disclaimer: This information is provided for informational purposes only and is not intended to diagnose, treat, or cure any condition. Always consult a licensed medical professional before making changes to your healthcare regimen.
Hyperhidrosis, or excessive sweating can be generalized, affecting the entire body, or focal, affecting specific areas such as the palms, armpits, soles, or face. (52F)
Eccrine Sweat Glands
Structure & Location: These are simple, coiled, tubular glands found throughout the body, with a high concentration on the soles of the feet. (52F)
Innervation & Function: Eccrine glands are stimulated by acetylcholine and the sympathetic nervous system. They receive sympathetic innervation via cholinergic (rather than adrenergic) fibers, which trigger sweating based on changes in core body temperature. (52F)
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Apocrine Sweat Glands
Structure & Location: These larger, branched glands are primarily located in the axillary (armpits) and perineal regions (including perianal areas, labia majora, scrotum, prepuce, nipples, and areolar tissue). (52F)
Innervation & Function: Apocrine glands are stimulated by norepinephrine, often producing malodorous perspiration. They are linked to emotion-induced sweating (e.g., stress, fear, pain, or sexual arousal). (52F)
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Treatment Options
The main goals in hyperhidrosis treatment are blocking acetylcholine (e.g. botulinum toxin or anticholinergics) and reducing stress responses (e.g. beta blockers).
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Anticholinergics such as Oxybutynin, blocks muscarinic receptors (particularly M1, M3, and M4) on both eccrine and apocrine sweat glands, reducing sweat production. They can produce side effects such as dry mouth, blurred vision from reduced tear production, constipation, and other symptoms due to reduced parasympathetic activity. (53F)
Botulinum Toxin A - Inhibits the release of acetylcholine at presynaptic terminals, halting sympathetic neurotransmission in sweat glands and thereby stopping excessive sweating. (54F)
Beta-Blockers (e.g., Propranolol) - Commonly prescribed for anxiety and stage fright. They lower heart rate and reduce stress-related symptoms like sweating and tremors. (55F)
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How different terpenes could affect hyperhidrosis
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Alpha-Pinene
Mechanism: α-Pinene is an acetylcholinesterase inhibitor. (5C,37E)
Effect on Sweating:
Worse for Cholinergic Sweating: By inhibiting the enzyme that breaks down acetylcholine, α-pinene could increase ACh levels, potentially increasing cholinergic sweating.
Possible Stress Reduction: Acetylcholinesterase inhibitors can induce a parasympathetic response,(65C) and increased parasympathetic tone can counteract some sympathetic-driven processes, α-pinene might also calm stress-related triggers; but it could still worsen sweating through increasing acetylcholine.
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Beta-Myrcene
Mechanisms: Mu-Opioid and α2-Adrenoreceptor Modulation (69C)
Effect on Sweating:
Reduced Sympathetic Tone: Activation of α2 receptors can lowers sympathetic outflow and can increase vagal (parasympathetic) tone. (52F)
Stress-Induced Sweating: By diminishing the stress (fight-or-flight) response, myrcene may help reduce sweating tied to anxiety, fear, or emotional triggers.
Relaxing Indica Terpene: Myrcene is a well known relaxing Indica terpene. It could help reduce stress-induced sweating by modulating both the mu-opioid and alpha 2-adrenoreceptor.
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Linalool
Mechanisms: Inhibits ACh Release at neuromuscular junctions (reducing channel open time), (55C) and a NMDA Receptor Antagonist. (12F,24F)
Effect on Sweating:
Cholinergic Pathway: By decreasing ACh release, linalool could reduce primary neurotransmitter for eccrine glands.
Neuroexcitation: As an NMDA antagonist, it could lower excitatory signaling,(23F,24F) further reducing stress-induced sweating.
Overall Impact: Could help both cholinergic and stress-related sweating.
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Terpineol
Mechanism: Anticholinergic (11D)
Effect on Sweating: Similar to prescription anticholinergics, terpineol could reduce excessive sweating by blocking muscarinic receptors on sweat glands.
May produce side effects typical of anticholinergics. Prescription anticholinergics can produce symptoms that include dry mouth rapid heart rate, arrhythmias, urinary retention, blurred vision, constipation, reduced gut motility, hyperthermia, and inhibition of sweating.(35C)
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A cannabis strain with myrcene, terpineol, and linalool could be a good choice to help with hyperhidrosis. Strains that could make sweating worse would have acetylcholinesterase inhibitors, which include:
Limonene IC(50)=390.2 ± 30.0 (37E)
Alpha-Pinene IC(50)=524.5 ± 42.4 (37E)
Beta-Caryophyllene IC(50)=436.0±29.9 (37E)
Beta-Caryophyllene Oxide IC(50)=320.16 ± 13.47 (37E)
Humulene IC(50)=785.3 ± 66.0 (37E)
Delta 3 Carene IC(50) not available (52C)
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Many strains have some of these ACh inhibitor terpenes with Indica’s that have more beneficial terpenes (myrcene, terpineol, and linalool), and depending on the concentration of each, one effect will take over. For example, Lemon Walker still gives me a lot of anticholinergic effects like dry mouth and eyes from the terpineol even though there is some limonene and a-pinene in it, and this strain does help reduce sweating.
Sources
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5C. Miyazawa M, Yamafuji C. Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids. J Agric Food Chem. 2005 Mar 9;53(5):1765-8. doi: 10.1021/jf040019b. PMID: 15740071.
35C. Ghossein N, Kang M, Lakhkar AD. Anticholinergic Medications. [Updated 2023 May 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK555893/
52C. Miyazawa M, Yamafuji C. Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids. J Agric Food Chem. 2005 Mar 9;53(5):1765-8. doi: 10.1021/jf040019b. PMID: 15740071.
55C. Re L, Barocci S, Sonnino S, Mencarelli A, Vivani C, Paolucci G, Scarpantonio A, Rinaldi L, Mosca E. Linalool modifies the nicotinic receptor-ion channel kinetics at the mouse neuromuscular junction. Pharmacol Res. 2000 Aug;42(2):177-82. doi: 10.1006/phrs.2000.0671. PMID: 10887049.
11D. Dos Santos Negreiros P, da Costa DS, da Silva VG, de Carvalho Lima IB, Nunes DB, de Melo Sousa FB, de Souza Lopes Araújo T, Medeiros JVR, Dos Santos RF, de Cássia Meneses Oliveira R. Antidiarrheal activity of α-terpineol in mice. Biomed Pharmacother. 2019 Feb;110:631-640. doi: 10.1016/j.biopha.2018.11.131. Epub 2018 Dec 9. PMID: 30540974.
37E. Hung NH, Quan PM, Satyal P, Dai DN, Hoa VV, Huy NG, Giang LD, Ha NT, Huong LT, Hien VT, Setzer WN. Acetylcholinesterase Inhibitory Activities of Essential Oils from Vietnamese Traditional Medicinal Plants. Molecules. 2022 Oct 20;27(20):7092. doi: 10.3390/molecules27207092. PMID: 36296686; PMCID: PMC9610647.
12F. Brum LF, Elisabetsky E, Souza D. Effects of linalool on [(3)H]MK801 and [(3)H] muscimol binding in mouse cortical membranes. Phytother Res. 2001 Aug;15(5):422-5. doi: 10.1002/ptr.973. PMID: 11507735.
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23F. Alkhachroum A, Der-Nigoghossian CA, Mathews E, Massad N, Letchinger R, Doyle K, Chiu WT, Kromm J, Rubinos C, Velazquez A, Roh D, Agarwal S, Park S, Connolly ES, Claassen J. Ketamine to treat super-refractory status epilepticus. Neurology. 2020 Oct 20;95(16):e2286-e2294. doi: 10.1212/WNL.0000000000010611. Epub 2020 Sep 1. PMID: 32873691; PMCID: PMC7713785.
24F. Jewett BE, Thapa B. Physiology, NMDA Receptor. [Updated 2022 Dec 11]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK519495/
52F. Hodge BD, Sanvictores T, Brodell RT. Anatomy, Skin Sweat Glands. [Updated 2022 Oct 10]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482278/
53F. Kudlak M, Tadi P. Physiology, Muscarinic Receptor. [Updated 2023 Aug 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK555909/
54F. Heckmann M, Ceballos-Baumann AO, Plewig G; Hyperhidrosis Study Group. Botulinum toxin A for axillary hyperhidrosis (excessive sweating). N Engl J Med. 2001 Feb 15;344(7):488-93. doi: 10.1056/NEJM200102153440704. PMID: 11172190.
55F. Farzam K, Jan A. Beta Blockers. [Updated 2023 Aug 22]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK532906/