Chance W T, von Meyenfeldt M, Fischer J E
Pharmacol Biochem Behav. 1983 Jan;18(1):115-21. doi: 10.1016/0091-3057(83)90260-5.
Anorectic tumor-bearing rats exhibited increased brain levels of the 5-HT precursor, tryptophan, and metabolite, 5-hydroxyindoleacetic acid (5-HIAA). In an effort to determine whether indoleamine systems had any role in the etiology of cancer anorexia the anorectic effects of cancer (Walker 256 carcinosarcoma) were investigated in immature female rats that had been depleted of brain serotonin (5-HT) by the intracisternal injection of 5,7-dihydroxytryptamine (5,7-DHT) or the systemic injection of para-chloramphetamine (PCA). Although both 5,7-DHT and PCA significantly reduced brain concentrations of 5-HT and 5-HIAA by approximately 50%, no effects on the onset or severity of the anorectic response to cancer were observed. Similarly, neither drug affected eating in non-tumor-bearing control animals. Therefore, these data do not support increased brain 5-HT activity as a primary mediator of cancer anorexia.
患有厌食症的荷瘤大鼠大脑中5-羟色胺(5-HT)前体色氨酸及其代谢产物5-羟吲哚乙酸(5-HIAA)的水平升高。为了确定吲哚胺系统在癌症厌食症病因中是否起作用,研究人员对未成熟雌性大鼠进行了研究,这些大鼠通过脑池内注射5,7-二羟基色胺(5,7-DHT)或全身注射对氯苯丙胺(PCA)耗尽了大脑中的血清素(5-HT),观察癌症(Walker 256癌肉瘤)的厌食作用。尽管5,7-DHT和PCA均使大脑中5-HT和5-HIAA的浓度显著降低了约50%,但未观察到对癌症厌食反应的发作或严重程度有任何影响。同样,这两种药物对未患肿瘤的对照动物的进食也没有影响。因此,这些数据不支持大脑5-HT活性增加是癌症厌食症的主要介导因素这一观点。