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《中国神经再生研究：英文版》
>Changes in P2Y purinoreceptor-mediated intracellular calcium signal pathways results in inositol-1, 4, 5-triphosphate-sensitive calcium stores in rat small trigeminal ganglion neurons
Changes in P2Y purinoreceptor-mediated intracellular calcium signal pathways results in inositol-1, 4, 5-triphosphate-sensitive calcium stores in rat small trigeminal ganglion neurons
BACKGROUND: Most of the currently available information on purinergic receptors (P2Rs) involved in pain transmission is based on results obtained in dorsal root ganglion or the spinal cord. However, the mechanism of P2Rs in trigeminal neuralgia remains unclear. OBJECTIVE: To investigate changes in the P2R-mediated calcium signaling pathway in nociceptive trigeminal ganglion neurons. DESIGN, TIME AND SETTING: In vitro experiments were conducted at the Patch-Clamp Laboratory of Comprehensive Experiment Center of Anhui Medical University, China from September 2008 to June 2009. MATERIALS: Thapsigargin, caffeine, suramin, and adenosine 5’-triphosphate were purchased from Sigma, USA. METHODS: Using Fura-2-based microfluorimetry, intracellular calcium concentration ([Ca2+]i) was measured in freshly isolated adult rat small trigeminal ganglion neurons before and after drug application. MAIN OUTCOME MEASURES: Fluorescent intensities were expressed as the ratio F340/F380 to observe [Ca2+]i changes. RESULTS: In normal extracellular solution and Ca2+-free solution, application of thapsigargin (1 μmol/L), a sarcoplasmic reticulum Ca2+ pump adenosine 5’-triphosphate inhibitor, as well as caffeine (20 mmol/L), a ryanodine receptor agonist, triggered [Ca2+]i increase in small trigeminal ganglion neurons. A similar response was induced by application of adenosine 5’-triphosphate (100 μmol/L). In Ca2+-free conditions, adenosine 5’-triphosphate-induced [Ca2+]i transients in small trigeminal ganglion neurons were inhibited in cells pre-treated with thapsigargin (P 0.05). In normal, extracellular solution, adenosine 5’-triphosphate-induced [Ca2+]i transients in small trigeminal ganglion neurons were partly inhibited in cells pre-treated with thapsigargin (P < 0.05). CONCLUSION: Inositol-1, 4, 5-triphosphate (IP3)- and ryanodine-sensitive Ca2+ stores exist in rat nociceptive trigeminal ganglion neurons. Two pathways are involved in the purinoreceptor-mediated [Ca2+]i rise observed in nociceptive trigeminal ganglion neurons. One pathway involves the metabotropic P2Y receptors, which are associated with the IP3 sensitive Ca2+store, and the second pathway is coupled to ionotropic P2X receptors that induce the Ca2+ influx.
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