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[14C]亚硝基去甲烟碱在小鼠组织中的定位

Localization of [14C]nitrosonornicotine in tissues of the mouse.

作者信息

Waddell W J, Marlowe C

出版信息

Cancer Res. 1980 Oct;40(10):3518-23.

PMID:7002288
Abstract

Male C57BL/6J mice were given i.v. injections of 7 mg (about 4 mu Ci) of N'-[pyrrolidine-2-14C] nitrosonornicotine per kg and frozen by immersion in dry ice:hexane at 0.1, 0.33, 1, 3, 9, and 24 hr after injection. The mice were processed for whole-body autoradiography without allowing thawing or the use of any solvents; sagittal sections of the frozen mice were freeze dried and placed on X-ray film to reveal areas of localization of radioactivity. At 6 min after administration, radioactivity was highest in liver, kidney, parotid gland, nasal epithelium, melanin, and contents of lower stomach; there was very little radioactivity at this time interval in bronchial epithelium. At later time intervals, there was increasing radioactivity in bronchial and nasal epithelium and sublingual and submandibular duct epithelium. By 24 hr after administration, virtually the only radioactivity remaining in the entire body was in the epithelium of the nasal cavity, bronchi, esophagus, and salivary glands and also in melanin, liver, proximal tubules of the kidney, and preputial gland. The autoradiographs are interpreted to reveal that most of the radioactivity is eliminated by renal and hepatic secretion and that metabolites are retained only at sites of carcinogenic action. The specificity of accumulation in nasal, bronchial, esophageal, and salivary duct epithelium may be due to receptor-directed interactions and suggests that other compounds might block this accumulation.

摘要

给雄性C57BL/6J小鼠静脉注射每千克7毫克(约4微居里)的N'-[吡咯烷-2-¹⁴C]亚硝基去甲烟碱,并在注射后0.1、0.33、1、3、9和24小时通过浸入干冰:己烷中进行冷冻。对小鼠进行全身放射自显影处理,不允许解冻或使用任何溶剂;将冷冻小鼠的矢状切片进行冷冻干燥并置于X射线胶片上,以显示放射性定位区域。给药后6分钟,肝脏、肾脏、腮腺、鼻上皮、黑色素和胃下部内容物中的放射性最高;在此时间间隔内,支气管上皮中的放射性很少。在随后的时间间隔中,支气管和鼻上皮以及舌下和下颌下导管上皮中的放射性增加。给药后24小时,全身几乎仅存的放射性位于鼻腔、支气管、食管和唾液腺的上皮中,以及黑色素、肝脏、肾近端小管和包皮腺中。放射自显影片被解读为显示大部分放射性通过肾脏和肝脏分泌消除,且代谢产物仅保留在致癌作用部位。鼻腔、支气管、食管和唾液导管上皮中积累的特异性可能归因于受体导向的相互作用,并表明其他化合物可能会阻止这种积累。

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