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P物质在缺血再灌注期间心肌功能障碍中的作用。

The role of substance P in myocardial dysfunction during ischemia and reperfusion.

作者信息

Chiao H, Caldwell R W

机构信息

Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912-2300, USA.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1996 Mar;353(4):400-7. doi: 10.1007/BF00261436.

Abstract

Impairment of myocardial contraction ("myocardial stunning") occurs during reperfusion after short ischemic periods. Substance P (SP) is widely distributed in heart and can be released by various stimuli including myocardial hypoxia. Our previous study shows SP has a negative inotropic effect in guinea pig heart. The objective of this study was to investigate whether SP contributes to the myocardial stunning after brief global ischemia. Guinea pig hearts in a Langendorff preparation were subjected to 15 min of global ischemia followed by 60 min reperfusion. Experiments were performed without and with pretreatment with neurokinin-1 (NK1) receptor antagonists, spantide (10(-6)M) or CP-99,994-01 (10(-6)M) in order to study the role of SP. Experiments were also performed in hearts which were perfused with atropine, phentolamine, and nadolol (10(-6)M each) to examine the role of neurotransmitters and autonomic receptors. A group of hearts obtained from capsaicin-pretreated guinea pigs was also investigated. Left ventricular developed pressure (LVDP), left ventricular end-diastolic pressure (LVEDP), heart rate, and perfusion pressure were monitored. At the end of reperfusion, the LVDP of control hearts recovered to only 55 +/- 6% (+/- SEM) of preischemic baseline and the LVEDP increased significantly (P > 0.05). With pretreatment with spantide or CP-99,994-01, LVDP recovered to 88 +/- 2% or 78 +/- 2% of the preischemic baseline, respectively. The LVEDP of these hearts was not different from preischemic baseline and much smaller than in control hearts. There were no differences in heart rate and perfusion pressure compared to baseline among all groups. Similar results were obtained in hearts perfused with autonomic blockers. However, recoveries of LVDP and LVEDP were faster in hearts perfused with autonomic blockers during the first 10 min of reperfusion. Pretreatment with capsaicin also significantly improved recovery of LVDP and LVEDP. In conclusion, substance P is involved in postischemic myocardial dysfunction and neurokinin-1 receptors mediate this action. The NK1 receptor antagonists may be useful in prevention of "myocardial stunning".

摘要

在短暂缺血后的再灌注过程中会发生心肌收缩功能受损(“心肌顿抑”)。P物质(SP)广泛分布于心脏,可由包括心肌缺氧在内的各种刺激释放。我们之前的研究表明,SP对豚鼠心脏有负性变力作用。本研究的目的是探讨SP是否在短暂全心缺血后导致心肌顿抑。采用Langendorff装置制备的豚鼠心脏经历15分钟全心缺血,随后再灌注60分钟。为研究SP的作用,实验分未用和用神经激肽-1(NK1)受体拮抗剂spantide(10⁻⁶M)或CP-99,994-01(10⁻⁶M)预处理两组进行。实验还在分别用阿托品、酚妥拉明和纳多洛尔(各10⁻⁶M)灌注的心脏中进行,以研究神经递质和自主受体的作用。还研究了一组来自辣椒素预处理豚鼠的心脏。监测左心室舒张末压(LVDP)、左心室舒张末压(LVEDP)、心率和灌注压。再灌注结束时,对照心脏的LVDP仅恢复到缺血前基线的55±6%(±SEM),LVEDP显著升高(P>0.05)。用spantide或CP-99,994-01预处理后,LVDP分别恢复到缺血前基线的88±2%或78±2%。这些心脏的LVEDP与缺血前基线无差异,且远小于对照心脏。与基线相比,所有组的心率和灌注压均无差异。在用自主神经阻滞剂灌注的心脏中也得到了类似结果。然而,在用自主神经阻滞剂灌注的心脏中,再灌注最初10分钟内LVDP和LVEDP的恢复更快。辣椒素预处理也显著改善了LVDP和LVEDP的恢复。总之,P物质参与缺血后心肌功能障碍,神经激肽-1受体介导这一作用。NK1受体拮抗剂可能有助于预防“心肌顿抑”。

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