Effects of Intravenous anesthetics on Phosphatidylinositol Response of Spinal Descending Inhibitory Pathways of Rat

静脉麻醉药对大鼠脊髓下降抑制通路磷脂酰肌醇反应的影响

• 批准号: 10671421
• 负责人: SHIBATA Osamu
• 金额: $ 1.98万
• 依托单位: Nagasaki University
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Scientific Research (C)
• 财政年份: 1998
• 资助国家: 日本
• 起止时间: 1998 至 2000
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-10671421/
• 关键词: Spinal cord; Intravenous anesthetics; Inositol monophosphate; Phosphatidylinositol response; イノシトールリン脂質; 麻酔薬; イノシトールソン脂質; クロニジン; カテコラミン; 気管平滑筋

Noradrenergic neurons arise from the locus coeruleus and project widely to the spinal cord, cerebral cortex andothers. Noradrenergic pathways in the spinal cord are considered to be one of the central descending inhibitory influences on spinal sensory transmission. Norepinephrine (NE) in the central nervous system has the effect to stimulate phosphatidylinositol (PI) response through aradrenergic receptors. The present study was designed to examine the effects of intravenous anesthetics on NE-induced PI response of rat spinal cords. Materials and Methods: Male Wistar ratsweighing 250-350 g were used for the experiments. , The rats were anesthetized with pentobarbital and their thoracic spinal cord was rapidly isolated. The spinal cord waschopped into 1-mm-wide slices. Three pieces of the slice were placed in small flat-bottomed tubes andincubated in K-H solution containing 5 mM LiCI. The effects of intravenous anesthetics on NE-induced inositol monophosphate (IP_1) accumulation were examined. We measured [^3H]IP_1 in spinal cord slices incubated with [^3H]myo-inositol with aliquid scintillation counter. Results : NE-induced IP_1 accumulation of spinal cord slices was attenuated dose-dependently by droperidol, but was not attenuated by ketamine, fentanyl and midazolam.

去甲肾上腺素能神经元来自基因座，并广泛地投射到脊髓，大脑皮层和thothorth。脊髓中的去肾上腺素能途径被认为是对脊柱感觉传递的中心降低抑制作用之一。中枢神经系统中的去甲肾上腺素（NE）具有通过阿雷肾上腺素受体刺激磷脂酰肌醇（PI）反应的作用。本研究旨在检查静脉麻醉药对大鼠脊髓NE诱导的PI反应的影响。材料和方法：使用250-350 g的雄性Wistar Ratswighs进行实验。 ，将大鼠用戊巴比妥麻醉，并迅速分离其胸椎。脊髓融合成1毫米宽的切片。将三块切片放在小的平底管中，并在含有5毫米lici的K-H溶液中孵育。检查了静脉麻醉药对NE诱导的肌醇一磷酸（IP_1）积累的影响。我们在脊髓切片中测量了[^3H] IP_1，该切片与[^3H]肌醇与中液闪烁计数器一起孵育。结果：NE诱导的IP_1脊髓切片的积累依赖于Droperidol依赖性剂量，但并未因氯胺酮，芬太尼和咪达唑仑的衰减而减弱。

项目成果

Iwanaga S, Shibata O, Tsuda A, Hashimoto S, Makita T, Cho S, Sumikawa K: "The role of alpha1 - adrenocedptors in the clonidine-induced contraction and relaxation of rat aorta"Res Commun Mol Pathol Pharmacol. 102(2). 137-47 (1998)

Iwanaga S、Shibata O、Tsuda A、Hashimoto S、Makita T、Cho S、Sumikawa K：“α1-肾上腺素受体在可乐定诱导的大鼠主动脉收缩和舒张中的作用”Res Commun Mol Pathol Pharmacol。

Shu Iwanaga: "The role of α_1-adrenoceptors in clonidine-induced contraction and relaxation of cut aorta" Research communications in molecular pathology and pharmacology. (in press).

Shu Iwanaga：“α_1-肾上腺素受体在可乐定诱导的主动脉收缩和舒张中的作用”分子病理学和药理学研究通讯（出版中）。

Shibata O, Saito M, Hashimoto S, Sakai K, Makita T, Sumikawa K: "Clonidine attenuates the carbachol-induced contractile and phosphatidylinositol responses of rat trachea"J. Pharm Parmacol. 52(12). 1523-8 (2000)

Shibata O、Saito M、Hashimoto S、Sakai K、Makita T、Sumikawa K：“可乐定减弱卡巴胆碱诱导的大鼠气管收缩和磷脂酰肌醇反应”J。

Shibata O, Saitgo M, Maekawa T, Shibata S, Makita T, Sumikawa K: "There is no direct relationship between PI response and smooth muscle contraction of rat trachea stimulated by alpha-agonists"Can J anaesth. 43(8). 830-1 (2001)

Shibata O、Saitgo M、Maekawa T、Shibata S、Makita T、Sumikawa K：“PI 反应与 α 激动剂刺激的大鼠气管平滑肌收缩之间没有直接关系”Can J anaesth。

Tsuda A, Shibata O, Saito M, Hashimoto S, Iwanaga S, Makita T, Sumikawa K: "A dose-response study of anticholinesterase drugs on contractile and phosphatidylinositol responses of rat trachea"Anesth Analg. 92(1). 100-5 (2001)

Tsuda A、Shibata O、Saito M、Hashimoto S、Iwanaga S、Makita T、Sumikawa K：“抗胆碱酯酶药物对大鼠气管收缩和磷脂酰肌醇反应的剂量反应研究”Anesth Analg。