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在PGE1诱导的体温过高期间,一氧化氮可降低体温以及减少对棕色脂肪组织的交感神经输入。

Nitric oxide reduces body temperature and sympathetic input to brown adipose tissue during PGE1-hyperthermia.

作者信息

Monda M, Amaro S, Sullo A, De Luca B

机构信息

Department of Human Physiology and Integrated Biological Function Filippo Bottazzi Second University of Naples, Italy.

出版信息

Brain Res Bull. 1995;38(5):489-93. doi: 10.1016/0361-9230(95)02020-r.

Abstract

The firing rate of the nerves innervating interscapular brown adipose tissue (IBAT) and IBAT and colonic temperatures (TIBAT and TC were monitored in urethane-anaesthetized male Sprague-Dawley rats. These variables were measured for 40 min before (baseline values) and 40 min after a 4 micromoles L-arginine (L-arg) or 400 nmoles nitroprusside (NP) injection in a lateral cerebral ventricle and an intracerebroventricular administration of 500 ng prostaglandin E1 (PGE1). The same variables were monitored in other rats with L-arg or NP or PGE1 administration alone. No drug was injected in control rats. The results show that L-arg or NP injection reduces the increases in firing rate, TIBAT, Tc induced by PGE1. These findings suggest that nitric oxide is important in the control of thermogenic changes during the PGE1 hyperthermia.

摘要

在氨基甲酸乙酯麻醉的雄性斯普拉格-道利大鼠中,监测支配肩胛间棕色脂肪组织(IBAT)的神经放电频率以及IBAT和结肠温度(TIBAT和TC)。在侧脑室注射4微摩尔L-精氨酸(L-arg)或400纳摩尔硝普钠(NP)以及脑室内给予500纳克前列腺素E1(PGE1)之前(基线值)和之后40分钟测量这些变量。在单独给予L-arg、NP或PGE1的其他大鼠中监测相同的变量。对照大鼠未注射任何药物。结果表明,注射L-arg或NP可降低PGE1诱导的放电频率、TIBAT和Tc的升高。这些发现表明,一氧化氮在PGE1热疗期间产热变化的控制中起重要作用。

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