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玛雪莉(一种热解烟草产品)在维生素A缺乏的斯普拉格-道利大鼠中的致癌性研究。

Carcinogenicity studies of masheri: pyrolysed tobacco product, in vitamin-A-deficient Sprague Dawley rats.

作者信息

Ammigan N, Nair U J, Lalitha V S, Bhide S V

机构信息

Carcinigenesis Division, Cancer Research Institute, Tata Memorial Centre, Parel, Bombay, India.

出版信息

J Cancer Res Clin Oncol. 1991;117(1):50-4. doi: 10.1007/BF01613196.

Abstract

The carcinogenicity of long-term feeding of masheri extract to animals in a vitamin-A-sufficient (SLO+) and deficient (SLO-) state was studied in Sprague Dawley rats by feeding daily dose of 3 mg extract over a period of 21 months. The phase I activating enzymes, the glutathione (GSH)/glutathione S-transferase (GST) detoxification system, and the hepatic and circulating levels of vitamins A and C were also monitored at 12 and 21 months. It was observed that the phase I enzyme activities were significantly higher in SLO+ than in SLO- rats at both 12 months and 21 months. Moreover, the SLO- masheri-treated animals also showed a decreased in the GSH/GST detoxification system while the reverse was observed in SLO+ group. Masheri extract treatment significantly lowered the hepatic and circulating levels of vitamin A while a concurrent increase was observed in the vitamin C level. The extract was found to be tumorigenic in both the SLO+ and SLO- groups. Benign tumours were observed in the SLO+ group while a high incidence of malignant tumours of the lung were observed in the SLO- group upon treatment with masheri extract.

摘要

通过在21个月的时间里每天给斯普拉格-道利大鼠喂食3毫克马舍里提取物,研究了在维生素A充足(SLO+)和缺乏(SLO-)状态下长期给动物喂食马舍里提取物的致癌性。在12个月和21个月时,还监测了I期激活酶、谷胱甘肽(GSH)/谷胱甘肽S-转移酶(GST)解毒系统以及肝脏和循环中维生素A和C的水平。观察到,在12个月和21个月时,SLO+大鼠的I期酶活性显著高于SLO-大鼠。此外,经马舍里提取物处理的SLO-动物的GSH/GST解毒系统也有所下降,而在SLO+组中观察到相反的情况。马舍里提取物处理显著降低了肝脏和循环中维生素A的水平,同时维生素C水平出现了相应升高。发现该提取物在SLO+和SLO-组中均具有致瘤性。在用马舍里提取物处理后,SLO+组中观察到良性肿瘤,而SLO-组中观察到肺部恶性肿瘤的高发病率。

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本文引用的文献

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Polycyclic aromatic hydrocarbon profiles of pyrolysed tobacco products commonly used in India.
Cancer Lett. 1984 Aug;24(1):89-94. doi: 10.1016/0304-3835(84)90084-3.

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