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http://dx.doi.org/10.4196/kjpp.2011.15.5.285

Glycine- and GABA-mimetic Actions of Shilajit on the Substantia Gelatinosa Neurons of the Trigeminal Subnucleus Caudalis in Mice  

Yin, Hua (Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University)
Yang, Eun-Ju (Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University)
Park, Soo-Joung (Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University)
Han, Seong-Kyu (Department of Oral Physiology, School of Dentistry and Institute of Oral Bioscience, Chonbuk National University)
Publication Information
The Korean Journal of Physiology and Pharmacology / v.15, no.5, 2011 , pp. 285-289 More about this Journal
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 $GABA_A$ 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 $GABA_A$ 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.
Keywords
Substantia gelatinosa neurons; Shilajit; Patch clamp; Glycine receptor; $GABA_A$ receptor;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
Times Cited By Web Of Science : 0  (Related Records In Web of Science)
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1 Schepetkin I, Khlebnikov A, Kwon BS. Medical drugs from humus matter: focus on mumie. Drug Dev Res. 2002;57:140- 159.   DOI   ScienceOn
2 Gobel S. Golgi studies of the neurons in layer II of the dorsal horn of the medulla (trigeminal nucleus caudalis). J Comp Neurol. 1978;180:395-413.   DOI   ScienceOn
3 Light AR, Perl ER. Reexamination of the dorsal root projection to the spinal dorsal horn including observations on the differential termination of coarse and fine fibers. J Comp Neurol. 1979;186:117-131.   DOI   ScienceOn
4 Light AR, Kavookjian AM. Morphology and ultrastructure of physiologically identified substantia gelatinosa (lamina II) neurons with axons that terminate in deeper dorsal horn laminae (III-V). J Comp Neurol. 1988;267:172-189.   DOI   ScienceOn
5 Pan YZ, Pan HL. Primary afferent stimulation differentially potentiates excitatory and inhibitory inputs to spinal lamina II outer and inner neurons. J Neurophysiol. 2004;91:2413-2421.   DOI   ScienceOn
6 Acharya SB, Frotan MH, Goel RK, Tripathi SK, Das PK. Pharmacological actions of Shilajit. Indian J Exp Biol. 1988;26: 775-777.
7 Tiwari P, Ramarao P, Ghosal S. Effects of Shilajit on the development of tolerance to morphine in mice. Phytother Res. 2001;15:177-179.   DOI   ScienceOn
8 Garedew A, Feist M, Schmolz E, Lamprecht I. Thermal analysis of mumiyo, the legendary folk remedy from the Himalaya region. Thermochimica Acta. 2004;417:301-309.   DOI   ScienceOn
9 Agarwal SP, Khanna R, Karmarkar R, Anwer MK, Khar RK. Shilajit: a review. Phytother Res. 2007;21:401-405.   DOI   ScienceOn
10 Jaiswal AK, Bhattacharya SK. Effects of Shilajit on memory, anxiety and brain monoamines in rats. Indian Journal of Pharmacology. 1992;24:12-17.
11 Ghosal S, Singh SK, Srivastava RS. Shilajit part 2. Biphenyl metabolites from Trifolium repens. J Chem Res. 1988;196:165- 166.
12 Charaka S, Sharma PV. Karaprchitiya RasayanaPada. 4th ed. Chowkhambha orientalia Chikitsasthana, Varanasi; 1998. 49-50 p.
13 Takeuchi A, Onodera K. Effect of bicuculline on the GABA receptor of the crayfish neuromuscular junction. Nat New Biol. 1972;236:55-56.
14 Ghosal S. Chemistry of shilajit, an immunomodulatory Ayurvedic Rasayana. Pure and Appl Chem. 1990;62:1285-1288.   DOI
15 Ali M, Sahrawat I, Singh O. Phytochemical investigation of Shilajit. India J Chem. 2004;43B:2217-2222.
16 Myers VB, Haydon DA. Ion transfer across lipid membranes in the presence of gramicidin A. II. The ion selectivity. Biochim Biophys Acta. 1972;274:313-322.   DOI   ScienceOn
17 Kyrozis A, Reichling DB. Perforated-patch recording with gramicidin avoids artifactual changes in intracellular chloride concentration. J Neurosci Methods. 1995;57:27-35.   DOI   ScienceOn
18 Bhattacharya SK, Ghosal S. Effect of Shilajit on rat brain monoamines. Phytotherapy Res. 1992;6:163-164.   DOI
19 Kreuter J, Shamenkov D, Petrov V, Ramge P, Cychutek K, Koch-Brandt C, Alyautdin R. Apolipoprotein-mediated transport of nanoparticle-bound drugs across the blood-brain barrier. J Drug Target. 2002;10:317-325.   DOI   ScienceOn
20 Kuffler SW, Edwards C. Mechanism of gamma aminobutyric acid (GABA) action and its relation to synaptic inhibition. J Neurophysiol. 1958;21:589-610.   DOI
21 Bowery NG, Hill DR, Hudson AL, Doble A, Middlemiss DN, Shaw J, Turnbull M. (.)Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptor. Nature. 1980;283:92-94.   DOI   ScienceOn
22 Lee J, Back SK, Lim EJ, Cho GC, Kim MA, Kim HJ, Lee MH, Na HS. Are spinal GABAergic elements related to the manifestation of neuropathic pain in rat? Korean J Physiol Pharmacol. 2010;14:59-69.   DOI
23 Ebihara S, Shirato K, Harata N, Akaike N. Gramicidin-perforated patch recording: GABA response in mammalian neurones with intact intracellular chloride. J Physiol. 1995;484:77- 86.   DOI
24 Rajendra S, Lynch JW, Schofield PR. The glycine receptor. Pharmacol Ther. 1997;73:121-146.   DOI   ScienceOn
25 Lynch JW. Molecular structure and function of the glycine receptor chloride channel. Physiol Rev. 2004;84:1051-1095.   DOI   ScienceOn
26 Bradaia A, Trouslard J. Nicotinic receptors regulate the release of glycine onto lamina X neurones of the rat spinal cord. Neuropharmacology. 2002;43:1044-1054.   DOI   ScienceOn
27 Bormann J, Hamill OP, Sakmann B. Mechanism of anion permeation through channels gated by glycine and gamma-aminobutyric acid in mouse cultured spinal neurones. J Physiol. 1987;385:243-286.   DOI
28 Sessle BJ. Mechanisms of trigeminal and occipital pain. Pain Rev. 1996;3:91-116.