Glycine- and GABA-mimetic Actions of Shilajit on the Substantia Gelatinosa Neurons of the Trigeminal Subnucleus Caudalis in Mice.
10.4196/kjpp.2011.15.5.285
- Author:
Hua YIN
1
;
Eun Ju YANG
;
Soo Joung PARK
;
Seong Kyu HAN
Author Information
1. Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University, Jeonju 561-756, Korea. skhan@jbnu.ac.kr
- Publication Type:Original Article
- Keywords:
Substantia gelatinosa neurons;
Shilajit;
Patch clamp;
Glycine receptor;
GABAA receptor
- MeSH:
6-Cyano-7-nitroquinoxaline-2,3-dione;
Animals;
Brain Stem;
Central Nervous System;
Chloride Channels;
Facial Pain;
Gluconates;
Mecamylamine;
Mice;
Minerals;
N-Methylaspartate;
Neurons;
Picrotoxin;
Potassium;
Receptors, Glutamate;
Receptors, Glycine;
Receptors, Nicotinic;
Resins, Plant;
Strychnine;
Substantia Gelatinosa;
Tetrodotoxin
- From:The Korean Journal of Physiology and Pharmacology
2011;15(5):285-289
- CountryRepublic of Korea
- Language:English
-
Abstract:
Shilajit, a medicine herb commonly used in Ayurveda, has been reported to contain at least 85 minerals in ionic form that act on a variety of chemical, biological, and physical stressors. The substantia gelatinosa (SG) neurons of the trigeminal subnucleus caudalis (Vc) are involved in orofacial nociceptive processing. Shilajit has been reported to be an injury and muscular pain reliever but there have been few functional studies of the effect of Shilajit on the SG neurons of the Vc. Therefore, whole cell and gramicidin-perfotrated patch clamp studies were performed to examine the action mechanism of Shilajit on the SG neurons of Vc from mouse brainstem slices. In the whole cell patch clamp mode, Shilajit induced short-lived and repeatable inward currents under the condition of a high chloride pipette solution on all the SG neurons tested. The Shilajit-induced inward currents were concentration dependent and maintained in the presence of tetrodotoxin (TTX), a voltage gated Na+ channel blocker, CNQX, a non-NMDA glutamate receptor antagonist, and AP5, an NMDA receptor antagonist. The Shilajit-induced responses were partially suppressed by picrotoxin, a GABAA receptor antagonist, and totally blocked in the presence of strychnine, a glycine receptor antagonist, however not affected by mecamylamine hydrochloride (MCH), a nicotinic acetylcholine receptor antagonist. Under the potassium gluconate pipette solution at holding potential 0 mV, Shilajit induced repeatable outward current. These results show that Shilajit has inhibitory effects on the SG neurons of Vc through chloride ion channels by activation of the glycine receptor and GABAA receptor, indicating that Shilajit contains sedating ingredients for the central nervous system. These results also suggest that Shilajit may be a potential target for modulating orofacial pain processing.
