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正常氧合组织中NAD(P)H硝基蓝四氮唑还原酶水平:一项将酶活性与放射性标记米索硝唑结合相关联的组织化学研究

NAD(P)H nitroblue tetrazolium reductase levels in apparently normoxic tissues: a histochemical study correlating enzyme activity with binding of radiolabelled misonidazole.

作者信息

Cobb L M, Hacker T, Nolan J

机构信息

MRC Radiobiology Unit, Didcot, Oxfordshire, UK.

出版信息

Br J Cancer. 1990 Apr;61(4):524-9. doi: 10.1038/bjc.1990.118.

Abstract

Hack and Helmy's method for the histochemical identification of NAD(P)H nitroblue tetrazolium reductase activity was employed to pinpoint reductase activity in certain cells in the mouse. High activity was observed in the following: lower airway epithelium, liver (centrilobular zone), eyelid (meibomian and sebaceous glands), vulval gland and parotid gland (striated cells of intralobular ducts). All of these cells had previously been identified as sites of binding of the reactive metabolites formed from the enzymic reduction of misonidazole (MISO) (Cobb et al., 1989). It had previously been thought that MISO binding would only take place in significant amounts in hypoxic tissues (tumour and possibly liver) since in normoxic tissues oxygen should reverse the initial one electron enzymic reduction, thus preventing progressive reduction to reactive species. We suggest that the very high levels of reductase in the above listed, probably normoxic, tissues contribute significantly to the accumulation of bound reactive MISO metabolite(s).

摘要

采用哈克和赫尔米的组织化学方法鉴定NAD(P)H硝基蓝四氮唑还原酶活性,以确定小鼠某些细胞中的还原酶活性。在以下部位观察到高活性:下呼吸道上皮、肝脏(小叶中心区)、眼睑(睑板腺和皮脂腺)、外阴腺和腮腺(小叶内导管的横纹肌细胞)。所有这些细胞先前已被确定为米索硝唑(MISO)酶促还原形成的反应性代谢产物的结合部位(科布等人,1989年)。以前人们认为,MISO结合只会在缺氧组织(肿瘤以及可能的肝脏)中大量发生,因为在正常氧合组织中,氧气应该会逆转最初的单电子酶促还原反应,从而阻止逐步还原为反应性物质。我们认为,上述列出的可能为正常氧合的组织中非常高的还原酶水平,对结合的反应性MISO代谢产物的积累有显著贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84bf/1971377/65943c22530c/brjcancer00224-0035-a.jpg

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