Effect of premedication on the changes of neuropeptide Y (NPY) in anesthesia.

C L Chang, Y C Tsai, S S Lin, J T Cheng
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Abstract

Premedication is one of the popular techniques in anesthesia, not only for the decrease of side effects but also for the increase of actions. Clinically, we found that plasma neuropeptide Y-like immunoreactivity (NPY-IR) was lowered in patients who had received premedication. In rats, plasma NPY-IR was not modified by the intravenous injection of diazepam. Pethidine reduced the plasma NPY-IR level which could be reversed by naloxone. Direct inhibition of plasma NPY-IR through an activation of opioid receptors can thus be considered. To the cold-stress stimulation, plasma NPY-IR was markedly raised. Diazepam reduced this stimulation-induced increase of plasma NPY-IR in a dose-dependent manner. Similar derivative of benzodiazepine produced an inhibition in a way following the potency as that to produce anxiolytic action. Also, this inhibition was reversed by PK11195, an antagonist of peripheral benzodiazepine receptors. Moreover, pain-stimulated increase of plasma NPY-IR in rats was also reduced by pethidine. This action was totally reversed in the presence of naloxone, indicating the participation of opioid receptors in the process. The obtained results suggest that premedication of diazepam and/or pethidine has the ability to decrease plasma NPY-IR in animals.

麻醉前用药对神经肽Y (NPY)变化的影响。
预用药是麻醉中常用的技术之一,不仅可以减少副作用,而且可以增加作用。在临床上,我们发现接受药物前治疗的患者血浆神经肽y样免疫反应性(NPY-IR)降低。在大鼠中,静脉注射地西泮不改变血浆NPY-IR。哌替啶可降低血浆NPY-IR水平,纳洛酮可逆转。因此,可以考虑通过激活阿片受体直接抑制血浆NPY-IR。在冷应激刺激下,血浆NPY-IR明显升高。地西泮以剂量依赖的方式降低了这种刺激引起的血浆NPY-IR的增加。苯二氮卓类药物的类似衍生物在某种程度上产生抑制作用,其效力与产生抗焦虑作用相同。此外,这种抑制作用被PK11195逆转,PK11195是外周苯二氮卓受体的拮抗剂。此外,哌替啶还能降低疼痛刺激大鼠血浆NPY-IR的升高。在纳洛酮的存在下,这一作用完全逆转,表明阿片受体参与了这一过程。本研究结果提示,预先给药地西泮和/或哌替啶能够降低动物血浆NPY-IR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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