Ernouf D, Compagnon P, Lothion P, Narcisse G, Bénard J Y, Daoust M
1-UFR Médecine Pharmacie de Rouen, Saint Etienne du Rouvray, France.
Life Sci. 1993;52(12):989-95. doi: 10.1016/0024-3205(93)90190-e.
We studied platelet 3H-serotonin uptake in 32 former alcoholics, withdrawn for from 1 month to 22 years, in their descendants (21.7 +/- 1.6 years old, n = 17; 10.9 +/- 0.7 years old; n = 19), and in respective control groups, paired in age and sex. All of the alcoholics presented high 3H-serotonin uptake (Vmax = 10.88 +/- 4.23 pmoles/10(8)pl/30 sec., vs. 0.93 +/- 0.15 pmole/10(8)pl/30 sec. Their descendants also showed high platelet serotonin uptake: 3.94 +/- 1.44 pmoles/10(8)pl/30 sec., vs. 0.93 +/- 0.15 pmoles/10(8)pl/30 sec. for adult descendants, and 5.99 +/- 2.23 vs. 0.84 +/- 0.15 pmole/10(8)pl/30 sec. for young descendants. All subjects were free of alcoholisation (biological parameters studied were blood ethanol concentration, gamma glutamyl transferase and mean corpuscular volume), and dependence of former alcoholics was evaluate by using, a posteriori, the CAGE test. In descendants, 28% of the subjects have Vmax values higher than the highest of the control group. Alcohol, in vitro, (54 mM) did not affect serotonin uptake in any group. These results indicate that in descendants of alcoholics, platelet serotonin uptake is altered, without modification of sensitivity to ethanol. The genetic basis of alcohol dependence could be linked with the platelet serotonin transport.
我们研究了32名戒酒时间从1个月至22年不等的既往酗酒者及其后代(成年后代21.7±1.6岁,n = 17;幼年后代10.9±0.7岁,n = 19)以及年龄和性别匹配的相应对照组的血小板3H-血清素摄取情况。所有酗酒者均表现出较高的3H-血清素摄取(Vmax = 10.88±4.23皮摩尔/10⁸血小板/30秒,而对照组为0.93±0.15皮摩尔/10⁸血小板/30秒)。他们的后代也表现出血小板血清素摄取较高:成年后代为3.94±1.44皮摩尔/10⁸血小板/30秒,而对照组为0.93±0.15皮摩尔/10⁸血小板/30秒;幼年后代为5.99±2.23皮摩尔/10⁸血小板/30秒,而对照组为0.84±0.15皮摩尔/10⁸血小板/30秒。所有受试者均未饮酒(所研究的生物学参数为血液乙醇浓度、γ-谷氨酰转移酶和平均红细胞体积),既往酗酒者的酒瘾通过事后使用CAGE测试进行评估。在后代中,28%的受试者Vmax值高于对照组的最高值。体外实验中,酒精(54 mM)对任何一组的血清素摄取均无影响。这些结果表明,在酗酒者的后代中,血小板血清素摄取发生改变,但对乙醇的敏感性未改变。酒精依赖的遗传基础可能与血小板血清素转运有关。