Gabapentin抗血小板凝集作用之機轉探討

Taipei Medical University Institutional Repository > 醫學院 > 醫學科學研究所 > 博碩士論文 > Item 987654321/5519

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题名:	Gabapentin抗血小板凝集作用之機轉探討 Mechanism involved in the antiplatelet effect of gabapentin
作者:	潘吉豐 Pan Chi Feng
贡献者:	醫學研究所
关键词:	gabapentin 血小板凝集 phosphoinositol breakdown TxA2 鈣離子 gabapentin platelet aggregation PI breakdown thromboxane A2 Ca2+
日期:	2003
上传时间:	2009-09-11 15:34:47 (UTC+8)
摘要:	Gabapentin (Neurontin) 是一種新的抗癲癇藥物，但是至今作用機轉仍然不清楚。有研究推測gabapentin可以改變血小板對serotonin的代謝或攝取（uptake）；然而，血小板在受刺激凝集的過程是否會受到gabapentin的影響，至今仍未有一套完整的研究加以證實。本研究在in vitro的實驗中發現外加gabapentin確實具有抑制血小板凝集之能力。並且在血小板凝集試驗中發現若事先外加gabapentin，確實有抑制由collagen、ADP、AA等血小板活化劑所引起的凝集作用；隨著血小板活化劑使用種類的不同，gabapentin之IC50約為120μM。本研究係探究gabapentin在血小板活化過程中對細胞內一些訊息傳遞的影響，亦即抑制血小板凝集之機轉。由研究結果發現gabapentin會隨著濃度之增加而有意義的抑制由不同血小板活化劑所引起的人類血小板之凝集現象；gabapentin會抑制由collagen所引起之血小板細胞內phosphoinositol breakdown；gabapentin會抑制由collagen所引起之血小板細胞內鈣離子的增加；再者gabapentin可抑制TxA2之形成，對AA的代謝路徑有所影響。由研究結果發現gabapentin抗血小板活化可能涉及以下路徑：gabapentin可藉由抑制phosphoinositol breakdown的pathway及影響TxA2之形成的pathway，進而影響細胞內鈣離子的移動，最後導致細胞內鈣離子的濃度減少而抑制血小板之凝集反應。關鍵字：Gabapentin，血小板凝集，phosphoinositol breakdown， TxA2，鈣離子 Gabapentin (Neurontin),in clinical use since 1993,is a novel antiepileptic drug. It is used clinically to reduce seizure frequency in patients with epilepsy. But the mechanism of action is not fully understood. Although its exact mechanism of action has yet to be determined, gabapentin is likely to have multiple effects. Nonepileptic use of gabapentin now accounts for roughly 40% of all reports on gabapentin. It has been previously speculated that gabapentin modulates the release of serotonin from blood platelets. But whether there is antiplatelet effect of gabapentin needs to be determined. In vitro study, gabapentin indeed inhibits the human platelet aggregation induced by various platelet inducers, such as collagen、ADP and arachidonic acid. Gabapentin also inhibits collagen-induced inositol monophosphate formation and inhibits collange-induced thromboxane A2 formation and intracellular Ca2+ mobilization. On account of these results, we speculate that the mechanism involved in signal transductions of platelet aggregation by gabapentin may be as the following: gabapentin may modulate the phosphoinositol breakdown pathway and thromboxane A2 formation pathway. Then may induce alteration in intracellular Ca2+ mobilization and reduce intracellular Ca2+ concentration and finally it may inhibit platelet activation. Key Words: gabapentin, platelet aggregation, PI breakdown thromboxane A2 , Ca2+
数据类型:	thesis
显示于类别:	[醫學科學研究所] 博碩士論文

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