Open Access
CC BY-NC-ND 4.0 · Planta Medica International Open 2019; 6(01): e23-e27
DOI: 10.1055/a-0871-2496
Original Papers
Eigentümer und Copyright ©Georg Thieme Verlag KG 2019

Evidence for Involvement of TRPV1 Receptors and Potassium Channels in the Seizures Induced by α-Sanshool

Benito Reyes-Trejo
1   Agricultural High School Department, Natural Products Laboratory, Chemistry Area, Autonomous University Chapingo, Chapingo, Mexico
,
Mario Noel Morales-Hernández
1   Agricultural High School Department, Natural Products Laboratory, Chemistry Area, Autonomous University Chapingo, Chapingo, Mexico
,
Gloria Melisa González-Anduaga
2   Faculty of Chemistry, Department of Pharmacy, National Autonomous University of Mexico, University City, Coyoacan 04510, Mexico City, Mexico
,
José Luis Balderas-López
2   Faculty of Chemistry, Department of Pharmacy, National Autonomous University of Mexico, University City, Coyoacan 04510, Mexico City, Mexico
,
José Carlos Tavares-Carvalho
3   Department of Biological Sciences and Health, Laboratory of Pharmaceutical Research, Pharmacy Course, Federal University of Amapa, Macapa, AP, Brazil
,
Andrés Navarrete
2   Faculty of Chemistry, Department of Pharmacy, National Autonomous University of Mexico, University City, Coyoacan 04510, Mexico City, Mexico
› Author Affiliations
Further Information

Publication History

received 27 September 2018
revised 28 February 2019

accepted 01 March 2019

Publication Date:
24 June 2019 (online)

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Abstract

α-Sanshool is an alkamide isolated from the stem bark of Zanthoxylum liebmannianum, a Mexican medicinal plant known as Colopahtle. Our research group has reported that the intraperitoneal administration of α-sanshool induces tonic-clonic seizures in mice. In the present study, we investigated the convulsive effect of this alkamide and elucidated its mechanism of action by comparing with well-known convulsive and anticonvulsive drugs in an in vivo approach. α-Sanshool showed a potent (ED50 [CL 95%]=3.06 [2.92–3.22] mg/kg) and immediate (2±2 s) seizure effect after the intraperitoneal administration in mice. The convulsive effect of this alkamide was only observed for intraperitoneal administration; the oral route did not show any effect. α-Sanshool was less potent than strychnine (ED50 [CL 95%]=1.53 [1.44–1.62] mg/kg), but more effective than bicuculline, 4-aminopyridine, affinin, and pentylenetetrazol, in that order. The seizures induced by α-sanshool were reduced by capsazepine and diazoxide, suggesting the involvement of TRPV1 and potassium channels in the mechanism of action of this compound.

Supporting Information