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育亨宾和哌唑嗪对去甲肾上腺素诱导的豚鼠耳部皮肤动脉各节段收缩的阻断作用存在差异。

Blockade of noradrenaline-induced constrictions by yohimbine and prazosin differs between consecutive segments of cutaneous arteries in guinea-pig ears.

作者信息

Morris J L

机构信息

Centre for Neuroscience, School of Medicine, Flinders University of South Australia, Adelaide.

出版信息

Br J Pharmacol. 1994 Dec;113(4):1105-12. doi: 10.1111/j.1476-5381.1994.tb17110.x.

Abstract
  1. The study has examined the receptors mediating constriction produced by brief local application of noradrenaline (NA) to cutaneous arteries and arterioles in the ear vasculature of anaesthetized guinea-pigs. The innervation of the corresponding vascular segments has been examined immunohistochemically at the conclusion of the pharmacological experiments. 2. Small arteries of branch order 4 (4 degrees, 40-110 microns internal diameter) were more sensitive to the vasoconstrictor action of NA than were more proximal arteries of branch order 3 (3 degrees, 60-150 microns internal diameter), or more distal arteries and arterioles of branch orders 5 to 7 (5 degrees-7 degrees, 18-85 microns internal diameter). This higher sensitivity of 4 degrees arteries was maintained after blockade of neuronal uptake with desipramine (1 microM), and after blockade of beta-adrenoceptors with propranolol (1 microM). 3. NA-induced vasoconstrictions of distal arterioles (5 degrees-7 degrees) were abolished or greatly reduced by yohimbine (1 microM). The blockade by yohimbine decreased progressively with increasing vessel diameter of proximal arteries, while the blockade by prazosin (1 microM) increased progressively in arteries > 40 microns diameter. 4. In 3 degrees and 4 degrees arteries, a substantial component (approximately 50%) of NA-induced vasoconstrictions remained after combined treatment with yohimbine and prazosin, in the presence or absence of desipramine. These constrictions were not further reduced by benextramine (1-10 microM), but were abolished by dihydroergotamine (1-10 microM). Constrictions induced by ATP (0.1-1 mM) were not affected by dihydroergotamine. 5. 5-Hydroxytryptamine (3-100 microM) had a variable effect on 3 degree and 4 degree arteries including: concentration dependent constrictions (n = 3); small constrictions at some concentrations, and dilatations or no change in diameter at other concentrations (n = 6); concentration-dependent dilatations only (n = 3). The 5-HT2 receptor antagonist, ketanserin (0.1-0.3 micro M), did not affect NA-induced constrictions.6. In 16 arterial segments ranging from 3 degree arteries to 60 arterioles, there was a significant correlation between the presence of neuropeptide Y-immunoreactive (NPY-IR) sympathetic axons and the degree of blockade of NA-induced constrictions by yohimbine, prazosin and dihydroergotamine.7. These results demonstrate marked differences in the postsynaptic adrenoceptors mediating vasoconstriction to a bolus of NA applied briefly to the adventitial surface of different segments of the cutaneous vasculature of the guinea-pig ear. Furthermore, the presence or absence of adrenoceptors sensitive to blockade by yohimbine or prazosin is related to the proportion of sympathetic axons innervating each vascular segment which contain NPY-IR.
摘要
  1. 本研究检测了在麻醉豚鼠耳部血管系统中,通过向皮肤动脉和小动脉局部短暂应用去甲肾上腺素(NA)所介导的收缩的受体。在药理学实验结束时,已通过免疫组织化学方法检测了相应血管段的神经支配情况。2. 分支等级为4级(4°,内径40 - 110微米)的小动脉对NA的血管收缩作用比分支等级更高的3级近端动脉(3°,内径60 - 150微米)或分支等级为5至7级(5° - 7°,内径18 - 85微米)的更远端动脉和小动脉更敏感。在用去甲丙咪嗪(1微摩尔)阻断神经元摄取后,以及用普萘洛尔(1微摩尔)阻断β - 肾上腺素能受体后,4°动脉的这种更高敏感性得以维持。3. 育亨宾(1微摩尔)可消除或显著降低NA诱导的远端小动脉(5° - 7°)的血管收缩。随着近端动脉直径增加,育亨宾的阻断作用逐渐减弱,而哌唑嗪(1微摩尔)的阻断作用在直径大于40微米的动脉中逐渐增强。4. 在3°和4°动脉中,在存在或不存在去甲丙咪嗪的情况下,联合使用育亨宾和哌唑嗪后,NA诱导的血管收缩仍有相当一部分(约50%)存在。这些收缩不受苯苄胺(1 - 10微摩尔)进一步影响,但被双氢麦角胺(1 - 10微摩尔)消除。ATP(0.1 - 1毫摩尔)诱导的收缩不受双氢麦角胺影响。5. 5 - 羟色胺(3 - 100微摩尔)对3°和4°动脉有不同影响,包括:浓度依赖性收缩(n = 3);在某些浓度下有小收缩,在其他浓度下有扩张或直径无变化(n = 6);仅浓度依赖性扩张(n = 3)。5 - HT2受体拮抗剂酮色林(0.1 - 0.3微摩尔)不影响NA诱导收缩。6. 在从3°动脉到60条小动脉的16个动脉段中,神经肽Y免疫反应性(NPY - IR)交感神经轴突的存在与育亨宾、哌唑嗪和双氢麦角胺对NA诱导收缩的阻断程度之间存在显著相关性。7. 这些结果表明,在豚鼠耳部皮肤血管不同节段的外膜表面短暂应用一剂NA所介导的血管收缩的突触后肾上腺素能受体存在显著差异。此外,对育亨宾或哌唑嗪阻断敏感的肾上腺素能受体的存在与否与支配每个血管段的含NPY - IR交感神经轴突的比例有关。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba48/1510510/5d94a40318f9/brjpharm00173-0040-a.jpg

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