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评估二羟基色胺和5-羟色胺拮抗剂作为细胞毒性剂对二甲基肼诱导的腺癌的细胞毒性。

Evaluation of the cytotoxicity of dihydroxytryptamines and 5-hydroxytryptamine antagonists as cytotoxic agents in dimethylhydrazine-induced adenocarcinomata.

作者信息

Tutton P J, Barkla D H

出版信息

Cancer Chemother Pharmacol. 1978;1(4):209-13. doi: 10.1007/BF00257151.

Abstract

The cytotoxicity of 5,6-dihydroxytryptamine (5,6-DHT), 5,7-dihydroxytryptamine (5,7-DHT), bromolysergic acid diethylamide (BOL), methysergide, and cyproheptadine, and also of 5,6-DHT together with either BOL, methysergide, or cyproheptadine in dimethylhydrazine-induced (DMH) carcinomata of rat colon was evaluated by estimating the percentage of necrotic cells in histological sections of tissues taken 15 h after injection of each of the drugs. In addition, the influence of methysergide and cyproheptadine on the tumour cell mitotic rate was estimated by means of a stathmokinetic technique. Both 5,6-DHT and 5,7-DHT were cytotoxic at each dose tested and for each of these agents the percentage of necrotic cells was directly correlated with the dose of drug used. BOL was not found to be cytotoxic to the colonic carcinomata, whereas both methysergide and cyproheptadine did cause detectable tumour cell necrosis. Methysergide was also found to accelerate tumour cell proliferation, whereas cyproheptadine did not. BOL competitively inhibited the cytotoxicity of 5,6-DHT and neither methysergide nor cyproheptadine potentiated the effect of 5,6 DHT.

摘要

通过估计在注射每种药物15小时后所取组织的组织学切片中坏死细胞的百分比,评估了5,6 - 二羟基色胺(5,6 - DHT)、5,7 - 二羟基色胺(5,7 - DHT)、溴麦角酰二乙胺(BOL)、美西麦角和赛庚啶,以及5,6 - DHT与BOL、美西麦角或赛庚啶联合使用对二甲基肼诱导的(DMH)大鼠结肠癌的细胞毒性。此外,通过一种有丝分裂抑制技术评估了美西麦角和赛庚啶对肿瘤细胞有丝分裂率的影响。5,6 - DHT和5,7 - DHT在每个测试剂量下均具有细胞毒性,并且对于这些药物中的每一种,坏死细胞的百分比与所用药物的剂量直接相关。未发现BOL对结肠癌具有细胞毒性,而美西麦角和赛庚啶均确实导致了可检测到的肿瘤细胞坏死。还发现美西麦角会加速肿瘤细胞增殖,而赛庚啶则不会。BOL竞争性抑制5,6 - DHT的细胞毒性,美西麦角和赛庚啶均未增强5,6 - DHT的作用。

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