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(+)-Pilocarpine is a muscarinic acetylcholine receptor agonist that binds to human hippocampal, pons, and submandibular gland membranes, which are endogenously enriched in the M1, M2, and M3 receptor subtypes, respectively (apparent Kis = 6, 8.2, and 6.9 μM, respectively).1 It induces salivary secretion in rats when administered intraperitoneally at a dose of 1 mg/kg.2 Topical administration of (+)-pilocarpine inhibits methylcellulose-induced increases in intraocular pressure in rabbits in a dose-dependent manner.3 (+)-Pilocarpine is a chemoconvulsant that has been used in the generation of temporal lobe epilepsy animal models.4,5,6 Formulations containing (+)-pilocarpine have been used in the treatment of elevated intraocular pressure and dry mouth.
WARNING This product is not for human or veterinary use.
1. Human M1-
2. Involvement of the central nervous system in the salivary secretion induced by pilocarpine in rats. J. Dent. Res. 72(11), 1481-1484 (1993).
3. The influence of epinephrine and pilocarpine upon intraocular pressure following single and combination installation. Ophthal. Res. 2(6), 328-336 (1971).
4. Neuroactive steroids protect against pilocarpine-
5. Disease-
6. NMDA receptor-
A non-