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吸烟者体内N-亚硝基脯氨酸的内源性形成。

Endogenous formation of N-nitrosoproline in cigarette smokers.

作者信息

Hoffmann D, Brunnemann K D

出版信息

Cancer Res. 1983 Nov;43(11):5570-4.

PMID:6616484
Abstract

It was the goal of this study to assay the potential of inhaled cigarette smoke for endogenous N-nitrosation of amines in smokers by means of measuring urinary excretion of N-nitrosoproline (NPRO). For 12 days, nonsmoking and smoking men were placed on a controlled diet which was relatively low in proline and in ascorbic acid. On Days 1 through 3, the volunteers received the controlled diet alone (Group 1); on Days 4 through 6, the diet was supplemented by a single daily dose of 300 mg of proline (Group 2); on Days 7 through 9, the diet was supplemented by a single daily dose of 1 g of ascorbic acid followed by 300 mg of proline (Group 3); and for the last 3 days, a single daily dose of 1 g ascorbic acid was given (Group 4). Collections of 24-hr urine were made on Days 3, 6, 9, and 12 of the study. The urine was analyzed for NPRO and creatinine and for cotinine, the major metabolite of nicotine. The mean 24-hr NPRO excretion for 13 nonsmokers in Group 1 was 3.6 micrograms. The NPRO excretion in 13 smokers in Group 1 was found to be 5.9 micrograms/24 hr, which is significantly higher than that of the nonsmokers (p less than 0.05). Urinary NPRO in 14 nonsmokers of Group 2 was significantly lower than that of the 14 smoking volunteers (p less than 0.05). Data for Group 3 indicated that those smokers who had shown elevated NPRO excretion in Group 2 had reduced urinary levels of NPRO as a consequence of ascorbic acid intake. Differences in NPRO excretion by smokers and nonsmokers on controlled diet with ascorbic acid but without proline supplements (Group 4) were also insignificant. These findings suggest that the documented endogenous N-nitrosation of proline which occurs as a result of cigarette smoke inhalation may also apply to other N-nitrosatable amines including nicotine and thus lead to in vivo formation of carcinogenic N-nitrosamines.

摘要

本研究的目的是通过测量尿中N-亚硝基脯氨酸(NPRO)的排泄量,来测定吸入香烟烟雾使吸烟者体内胺类发生内源性亚硝化作用的可能性。在12天里,让不吸烟和吸烟的男性食用一种脯氨酸和抗坏血酸含量相对较低的对照饮食。在第1天至第3天,志愿者仅食用对照饮食(第1组);在第4天至第6天,饮食中每天补充一剂300毫克脯氨酸(第2组);在第7天至第9天,饮食中每天先补充一剂1克抗坏血酸,然后补充300毫克脯氨酸(第3组);在最后3天,每天补充一剂1克抗坏血酸(第4组)。在研究的第3天、第6天、第9天和第12天收集24小时尿液。对尿液进行NPRO、肌酐以及可替宁(尼古丁的主要代谢产物)的分析。第1组13名不吸烟者的平均24小时NPRO排泄量为3.6微克。发现第1组13名吸烟者的NPRO排泄量为5.9微克/24小时,显著高于不吸烟者(p<0.05)。第2组14名不吸烟者的尿NPRO显著低于14名吸烟志愿者(p<0.05)。第3组的数据表明,那些在第2组中显示NPRO排泄量升高的吸烟者,由于摄入抗坏血酸,尿中NPRO水平降低。在食用含抗坏血酸但不补充脯氨酸的对照饮食时(第4组),吸烟者和不吸烟者的NPRO排泄差异也不显著。这些发现表明,因吸入香烟烟雾而记录在案的脯氨酸内源性亚硝化作用,可能也适用于包括尼古丁在内的其他可亚硝化的胺类,从而导致体内致癌性N-亚硝胺的形成。

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