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中枢钙离子通道阻滞可逆转乙醇诱导的大鼠体温过低。

Central Ca++-channel blockade reverses ethanol-induced poikilothermia in the rat.

作者信息

Rezvani A H, Mack C M, Crovi S I, Myers R D

出版信息

Alcohol. 1986 Jul-Aug;3(4):273-9. doi: 10.1016/0741-8329(86)90037-6.

DOI:10.1016/0741-8329(86)90037-6
PMID:3755956
Abstract

Two series of experiments were performed to determine the possible involvement of Ca++ channels in the thermolytic action of ethanol administered at a room temperature of 22 degrees C. In one group of 11 adult female Sprague-Dawley rats, stainless steel guide cannulae were implanted stereotaxically above the lateral cerebral ventricle. Prior to an experiment, a thermistor probe was inserted into the colon so that core temperature could be monitored continuously for up to six hours or until the temperature had returned to a previous baseline level. When the animal's body temperature had stabilized, a dose of 4.0 g/kg in a v/v solution of 20% ethanol was given by intragastric gavage. After the body temperature had declined by about 2.0 degrees C, ordinarily 30 min after ethanol administration, either control CSF or the vehicle plus one of four doses of verapamil (8.3, 25, 50 and 100 micrograms) was infused intracerebroventricularly (ICV) in a volume of 10 microliter. In a second group of 7 unoperated rats, either 4.0 g/kg ethanol or a physiological saline control solution was administered isovolumetrically by intragastric gavage; then, 30 min later, either 3.0 or 10.0 mg/kg verapamil was injected intraperitoneally. At an ambient temperature of 22 degrees C, ethanol gavage produced a significant decline in colonic temperature which was unaffected by physiological saline given by the same route. Although the CSF control vehicle was without effect, verapamil administered ICV attenuated the thermolytic action of ethanol in all doses tested; however, the lowest dose exerted its antagonist effect but with a longer latency. Conversely, when verapamil was given systemically, the hypothermic action of ethanol was significantly potentiated in a dose-dependent manner.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

进行了两组实验,以确定在22摄氏度室温下给予乙醇的热解作用中Ca++通道可能的参与情况。在一组11只成年雌性Sprague-Dawley大鼠中,将不锈钢引导套管立体定向植入大脑侧脑室上方。在实验前,将热敏电阻探头插入结肠,以便连续监测核心温度长达6小时或直至温度恢复到先前的基线水平。当动物体温稳定后,通过胃内灌胃给予20%乙醇的v/v溶液,剂量为4.0 g/kg。体温下降约2.0摄氏度后,通常在给予乙醇后30分钟,将对照脑脊液或载体加四种剂量之一的维拉帕米(8.3、25、50和100微克)以10微升的体积脑室内注射(ICV)。在第二组7只未手术的大鼠中,通过胃内灌胃等容给予4.0 g/kg乙醇或生理盐水对照溶液;然后,30分钟后,腹腔注射3.0或10.0 mg/kg维拉帕米。在22摄氏度的环境温度下,乙醇灌胃导致结肠温度显著下降,而相同途径给予生理盐水对此无影响。虽然脑脊液对照载体无效,但脑室内给予维拉帕米在所有测试剂量下均减弱了乙醇的热解作用;然而,最低剂量发挥其拮抗作用但潜伏期更长。相反,当全身给予维拉帕米时,乙醇的低温作用以剂量依赖性方式显著增强。(摘要截断于250字)

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