Stein L, Wise C D
Science. 1971 Mar 12;171(3975):1032-6. doi: 10.1126/science.171.3975.1032.
Single or repeated intraventricular injections of 6-hydroxydopamine caused marked and long-lasting deficits in brain self-stimulation and other rewarded behaviors in the rat. The behavioral deficits, as well as the depletion of brain norepinephrine induced by 6-hydroxydopamine, were prevented by prior treatment with chlorpromazine. Episodic or continuous formation of endogenous 6-hydroxydopamine in man as a result of a genetically determined enzymatic error could selectively damage the binding capacity and, eventually, the structural integrity of the noradrenergic reward mechanism. Such damage might cause the fundamental symptoms and long-term downhill course of schizophrenia.
向大鼠脑室内单次或重复注射6-羟基多巴胺会导致脑自我刺激及其他奖赏行为出现明显且持久的缺陷。6-羟基多巴胺所致的行为缺陷以及脑去甲肾上腺素耗竭,可通过事先给予氯丙嗪来预防。由于基因决定的酶错误,人类内源性6-羟基多巴胺的间歇性或持续性形成可能会选择性地损害去甲肾上腺素能奖赏机制的结合能力,并最终损害其结构完整性。这种损害可能会导致精神分裂症的基本症状和长期恶化病程。