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突触前阿片样物质OP4和大麻素CB1受体对脊髓麻醉大鼠心脏自主神经传递的调节作用

Modulation of the cardiac autonomic transmission of pithed rats by presynaptic opioid OP4 and cannabinoid CB1 receptors.

作者信息

Malinowska B, Piszcz J, Koneczny B, Hryniewicz A, Schlicker E

机构信息

Department of Experimental Physiology, Medical Academy, ul. Mickiewicza 2A, 15-230 Białystok 8, Poland.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2001 Sep;364(3):233-41. doi: 10.1007/s002100100450.

Abstract

We studied the effects of nociceptin, the endogenous ligand of the opioid OP4 receptor, and of two cannabinoid receptor agonists WIN 55,212-2 and CP-55,940 (0.001-1 micromol/kg each) on the neurogenic tachycardia and bradycardia in pithed rats. Electrical stimulation (1 Hz, 1 ms, 50 V for 10 s) of the preganglionic sympathetic nerve fibres and injection of nicotine 2 micromol/kg or isoprenaline 0.5 nmol/kg increased heart rate by about 70 beats/min (bpm) in pithed rats pretreated with atropine 1.5-2 micromol/kg. The electrically induced tachycardia was reduced dose dependently by nociceptin, WIN 55,212-2 and CP-55,940 (by 60, 30 and 20% at the highest dose, respectively). The OP4 and cannabinoid receptor agonists diminished the nicotine- but not the isoprenaline-stimulated increase in heart rate. In pithed rats pretreated with propranolol 3 micromol/kg, vagal stimulation (5 Hz, 1 ms, 15 V for 10 s) or injection of methacholine (5-10 nmol/kg) decreased heart rate by about 30 bpm. Nociceptin, but not WIN 55,212-2 or CP-55,940 decreased the vagal bradycardia dose dependently (the inhibitory effect of 1 micromol/kg was about 40%). Nociceptin failed to modify the methacholine-induced decrease in heart rate. The OP4 receptor antagonists naloxone benzoylhydrazone 5 micromol/kg and/or [Phe1Psi(CH2-NH)Gly2]-nociceptin(1-13)NH2 0.7 micromol/kg, but not the OP(1-3) receptor antagonist naloxone 10 micromol/kg, diminished the inhibitory action of nociceptin on the neurogenic tachycardia and bradycardia. The inhibitory effect of both cannabinoid receptor agonists on the neurogenic tachycardia was abolished by the CB1 receptor antagonist SR 141716 0.1 micromol/kg. The present data suggest that the postganglionic sympathetic nerve fibres innervating the rat heart are endowed with presynaptic opioid OP4 and cannabinoid CB1 receptors, activation of which inhibits the neurogenic tachycardia. The parasympathetic nerve fibres innervating the heart and causing bradycardia are endowed with presynaptic opioid OP4 but not cannabinoid receptors.

摘要

我们研究了阿片样物质OP4受体的内源性配体孤啡肽以及两种大麻素受体激动剂WIN 55,212-2和CP-55,940(每种剂量为0.001 - 1微摩尔/千克)对脊髓麻醉大鼠神经源性心动过速和心动过缓的影响。对经1.5 - 2微摩尔/千克阿托品预处理的脊髓麻醉大鼠,刺激节前交感神经纤维(1赫兹,1毫秒,50伏,持续10秒)以及注射2微摩尔/千克尼古丁或0.5纳摩尔/千克异丙肾上腺素可使心率增加约70次/分钟(bpm)。孤啡肽、WIN 55,212-2和CP-55,940可剂量依赖性地降低电刺激诱发的心动过速(最高剂量时分别降低60%、30%和20%)。OP4和大麻素受体激动剂可减弱尼古丁刺激引起的心率增加,但对异丙肾上腺素刺激引起的心率增加无影响。在经3微摩尔/千克普萘洛尔预处理的脊髓麻醉大鼠中,迷走神经刺激(5赫兹,1毫秒,15伏,持续10秒)或注射5 - 10纳摩尔/千克乙酰甲胆碱可使心率降低约30 bpm。孤啡肽可剂量依赖性地降低迷走神经诱发的心动过缓(1微摩尔/千克的抑制作用约为40%),而WIN 55,212-2和CP-55,940则无此作用。孤啡肽未能改变乙酰甲胆碱引起的心率降低。5微摩尔/千克的OP4受体拮抗剂纳洛酮苯甲酰腙和/或0.7微摩尔/千克的[Phe1Psi(CH2-NH)Gly2]-孤啡肽(1-13)NH2可减弱孤啡肽对神经源性心动过速和心动过缓的抑制作用,但10微摩尔/千克的OP(1-3)受体拮抗剂纳洛酮则无此作用。0.1微摩尔/千克的CB1受体拮抗剂SR 141716可消除两种大麻素受体激动剂对神经源性心动过速的抑制作用。目前的数据表明,支配大鼠心脏的节后交感神经纤维具有突触前阿片样物质OP4和大麻素CB1受体,激活这些受体可抑制神经源性心动过速。支配心脏并引起心动过缓的副交感神经纤维具有突触前阿片样物质OP4受体,但不具有大麻素受体。

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