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食欲素能系统在大鼠急性出血中的作用。

Role of the orexinergic system in acute haemorrhage in the rat.

作者信息

Hirota Kazuyoshi, Kushikata Tetsuya, Yoshida Hitoshi, Kudo Mihoko, Kudo Tsuyoshi

机构信息

Department of Anesthesiology, Hirosaki University Graduate School of Medicine, Hirosaki 036-8563, Japan.

出版信息

Neurosci Lett. 2008 Feb 20;432(2):162-6. doi: 10.1016/j.neulet.2007.12.015. Epub 2008 Jan 9.

Abstract

Orexins (OXs) stimulate sympathetic nerve activity to increase arterial pressure (AP) and heart rate (HR). We have previously reported that the OX(1)-receptor antagonist SB-334867 reversed the sympathomimetic actions of orexin A (OXA). In the present study we have investigated the role(s) of the orexinergic system in sympathetic activation during haemorrhage in rats. Sixteen Wistar rats, anaesthetised with pentobarbital, were assigned to 2 groups: saline i.p. (group S) and SB-334867 30 mg/kg i.p. (group SB) n=8 each. Haemorrhagic shock was established by acute withdrawal of 10 ml/kg of blood via an arterial catheter three times with a 30 min interval between each withdrawal. Haemodynamics were assessed 30 min after 10, 20, and 30 ml/kg of blood withdrawal. In addition, plasma orexin A and catecholamine concentrations in the shed blood were determined. In both groups, mean AP (MAP) and HR decreased significantly. Plasma catecholamine concentrations significantly increased following blood withdrawal. The reduction in MAP/HR and elevation of catecholamine levels were dependent on the total amount of shed blood. There were no differences between the groups. Plasma OXA concentrations increased to a greater extent in group SB than group S in response to haemorrhage. There was a significant correlation between plasma catecholamines and %change in MAP (epinephrine: r=0.553, p=0.0001, norepinephrine: r=0.374, p=0.0087) and HR (epinephrine: r=0.403, p=0.005, norepinephrine: r=0.436, p=0.002). There was no correlation with plasma orexin A levels. These data suggest that despite a weak activation the orexinergic system is unlikely to make a major contribution to the response to haemorrhage.

摘要

食欲素(OXs)刺激交感神经活动,以升高动脉压(AP)和心率(HR)。我们之前曾报道,OX(1)受体拮抗剂SB - 334867可逆转食欲素A(OXA)的拟交感神经作用。在本研究中,我们调查了食欲素能系统在大鼠出血期间交感神经激活中的作用。16只经戊巴比妥麻醉的Wistar大鼠被分为2组:腹腔注射生理盐水(S组)和腹腔注射30 mg/kg SB - 334867(SB组),每组n = 8。通过动脉导管以每次间隔30分钟急性抽取10 ml/kg血液,共抽取3次,建立失血性休克模型。在抽取10、20和30 ml/kg血液后30分钟评估血流动力学。此外,测定失血中血浆食欲素A和儿茶酚胺浓度。两组中,平均动脉压(MAP)和心率均显著下降。失血后血浆儿茶酚胺浓度显著升高。MAP/HR的降低和儿茶酚胺水平的升高取决于失血量。两组间无差异。出血后,SB组血浆OXA浓度升高幅度大于S组。血浆儿茶酚胺与MAP的变化百分比(肾上腺素:r = 0.553,p = 0.0001;去甲肾上腺素:r = 0.374,p = 0.0087)及心率(肾上腺素:r = 0.403,p = 0.005;去甲肾上腺素:r = 0.436,p = 0.002)之间存在显著相关性。与血浆食欲素A水平无相关性。这些数据表明,尽管食欲素能系统有轻度激活,但不太可能对出血反应起主要作用。

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