Overstreet D H, Lee Y W, Rezvani A H, Pei Y H, Criswell H E, Janowsky D S
Skipper Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill 27599-7178, USA.
Alcohol Clin Exp Res. 1996 Apr;20(2):221-7. doi: 10.1111/j.1530-0277.1996.tb01633.x.
The Chinese herbal medicine, NPI-028, has been used for centuries in China to counteract alcohol intoxication. The present study used a number of different experimental conditions to determine whether NPI-028 and its derivatives might selectively influence alcohol intake in rodents that naturally exhibit high alcohol intakes. It was determined that intraperitoneal (i.p.) injections of NPI-028 (0.5, 0.75, and 1.0 g/kg) suppressed alcohol intake by up to 30% in both alcohol-preferring P and Fawn-Hooded (FH) rats during a continuous access schedule. These injections did not significantly affect food or water intakes, nor did the highest dose of NPI-028 (1 g/kg) alter blood ethanol levels after an i.p. injection of 2.5 g/kg of ethanol. In P rats, it was found that NPI-028 was orally active with the dose of 1.5 g/kg having a greater effect on ethanol intake than the 1.0 g/kg dose; once again, food and water intakes were not significantly altered. In FH rats maintained on a limited access schedule (1 hr/day), alcohol intake was completely abolished by 1.5 g/kg of NPI-028. Chronic i.p. administration of NPI-028 (0.75 g/kg) for four consecutive days in FH rats maintained on a continuous access schedule did not lead to any diminution of its alcohol-suppressant effects. Thus, NPI-028 has significant effects on alcohol intake without much effect on water and food intake, and tolerance does not readily develop to these effects. The i.p. administration of a partially purified extract (NPI-031) of NPI-028, obtained by countercurrent chromatography, also dose-dependently suppressed ethanol intake in FH rats, but the highest dose 200 mg/kg) also significantly decreased food intake. Finally, the i.p. administration of puerarin (NPI-31G), an isoflavone isolated from NPI-031 by countercurrent chromatography, significantly reduced ethanol intake in FH rats without affecting food or water intake. Therefore, NPI-028 and one of its pure components, NPI-031G, selectively reduced ethanol intake in alcohol-preferring rats.
中草药NPI - 028在中国已使用了数百年,用于对抗酒精中毒。本研究采用了多种不同的实验条件,以确定NPI - 028及其衍生物是否可能选择性地影响自然表现出高酒精摄入量的啮齿动物的酒精摄入量。结果表明,在连续获取酒精的实验安排下,对偏好酒精的P大鼠和小鹿斑鼠(FH)腹腔注射NPI - 028(0.5、0.75和1.0 g/kg)可使酒精摄入量降低多达30%。这些注射对食物或水的摄入量没有显著影响,腹腔注射2.5 g/kg乙醇后,最高剂量的NPI - 028(1 g/kg)也未改变血液乙醇水平。在P大鼠中,发现NPI - 028口服有效,1.5 g/kg剂量对乙醇摄入量的影响大于1.0 g/kg剂量;同样,食物和水的摄入量没有显著改变。在按有限获取计划(每天1小时)饲养的FH大鼠中,1.5 g/kg的NPI - 028可完全消除酒精摄入量。在按连续获取计划饲养的FH大鼠中,连续四天腹腔注射NPI - 028(0.75 g/kg)不会导致其酒精抑制作用减弱。因此,NPI - 028对酒精摄入量有显著影响,而对水和食物摄入量影响不大,且这些作用不易产生耐受性。通过逆流色谱法获得的NPI - 028部分纯化提取物(NPI - 031)腹腔注射也能剂量依赖性地抑制FH大鼠的乙醇摄入量,但最高剂量(200 mg/kg)也显著降低了食物摄入量。最后,腹腔注射通过逆流色谱法从NPI - 031中分离出的异黄酮葛根素(NPI - 31G)可显著降低FH大鼠的乙醇摄入量,而不影响食物或水的摄入量。因此,NPI - 028及其一种纯成分NPI - 031G可选择性降低偏好酒精大鼠的乙醇摄入量。