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吗啡耐受和依赖大鼠肠道运动障碍的外周机制

Peripheral mechanisms of intestinal dysmotility in the morphine tolerant and dependent rats.

作者信息

Banach T, Zurowski D, Gil K, Weisbrodt N W, Rosenfeld G, Thor P J

机构信息

Dept. of Pathophysiology, Jagiellonian University Medical College, Cracow, Poland.

出版信息

J Physiol Pharmacol. 2006 Mar;57(1):73-82.

Abstract

Changes of intestinal motility and transit produced by tolerance to and dependence upon morphine have been partly attributed to peripheral mechanisms. We evaluated the effect of chronic peripheral morphine administration and peripheral mu-receptor blockade on vagal afferent activity (VAA) and c-Kit positive intramuscular cells of Cajal (ICCs). Ten rats were subjected to chronic subcutaneous morphine infusion for 72 h with subsequent VAA recording. Potential frequency was evaluated within recordings before and after mu receptor blockade by (D)-Phe -Cys -Tyr -(D)-Trp -Orn -Thr -Phe -Thr (CTOP) i.p. injections. Afterwards the rats were sacrificed and intramuscular c-Kit antigen expression was assessed by image analysis within removed fragments of duodenum and ascending colon. An equal group of rats served as a control for VAA and c-Kit expression. Analysis of VAA revealed similar frequencies of potentials in morphine tolerant / dependent rats before CTOP and in the controls. CTOP increased potential frequency in the morphine group which effect was visible mostly within the first 20 minutes (p=0.01). The morphine infused animals presented also higher c-Kit expression in both the duodenum (p<0.001) and the ascending colon (p<0.001) in comparison to the control group. Results of our study may indicate the involvement of both the intestinal wall and the long vago-vagal reflexes in tolerance to and dependence upon opioids.

摘要

对吗啡产生耐受性和依赖性所导致的肠道运动和传输变化,部分归因于外周机制。我们评估了慢性外周给予吗啡以及外周μ受体阻断对迷走神经传入活动(VAA)和Cajal肌内阳性细胞(ICC)的影响。十只大鼠接受了72小时的慢性皮下吗啡输注,随后记录VAA。通过腹腔注射(D)-苯丙氨酸-半胱氨酸-酪氨酸-(D)-色氨酸-鸟氨酸-苏氨酸-苯丙氨酸-苏氨酸(CTOP)阻断μ受体前后,在记录中评估电位频率。之后处死大鼠,通过图像分析评估十二指肠和升结肠切除片段内的肌内c-Kit抗原表达。另一组同等数量的大鼠作为VAA和c-Kit表达的对照。对VAA的分析显示,CTOP给药前,吗啡耐受/依赖大鼠的电位频率与对照组相似。CTOP增加了吗啡组的电位频率,这种效应主要在最初20分钟内可见(p = 0.01)。与对照组相比,接受吗啡输注的动物在十二指肠(p < 0.001)和升结肠(p < 0.001)中也表现出更高的c-Kit表达。我们的研究结果可能表明肠壁和长迷走-迷走反射均参与了对阿片类药物的耐受性和依赖性。

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