Anisimov V N, Pozdeev V K, Dmitrievskaia A Iu, Gracheva G M, Il'in A P
Vopr Onkol. 1977;23(7):34-9.
Thirty minutes after the administration of DMBA (5 mg i. v.) to rats the level of norepinephrine, dopamine, serotonine (5-HT) and 5-IIIAA in the hypothalamus was decreased, while monoamines levels in the brain stem and hemispheres was unchanged. After benz(a) anthracene (5 mg i.v.) treatment the level of 5-HT in rat hypothalamus was decreased, but catecholamines and 5-HIAA levels were not changed. Pretreatment with L-DOPA abolished the elevation of the threshold of hypothalamic sensitivity to estrogen suppression, induced by 20-methylcholanthrene in rats, and alpha-methyl-DOPA enhanced. It is suggested that the central (hypothalamic) mechanisms participate in the release of the carcinogenic effect of polycylic hydrocarbons in rats.
给大鼠静脉注射5毫克二甲基苯蒽(DMBA)30分钟后,下丘脑去甲肾上腺素、多巴胺、血清素(5-羟色胺,5-HT)和5-羟吲哚乙酸(5-HIAA)水平降低,而脑干和大脑半球中的单胺水平未变。用苯并(a)蒽(5毫克静脉注射)处理后,大鼠下丘脑5-HT水平降低,但儿茶酚胺和5-HIAA水平未改变。左旋多巴预处理消除了20-甲基胆蒽诱导的大鼠下丘脑对雌激素抑制敏感性阈值的升高,而α-甲基多巴增强了该阈值升高。提示中枢(下丘脑)机制参与了多环烃对大鼠致癌作用的释放。