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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=CBR1</id>
	<title>CBR1 - История изменений</title>
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	<updated>2026-08-02T10:27:25Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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	<entry>
		<id>https://transhumanist.ru/index.php?title=CBR1&amp;diff=6056&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Carbonyl reductase [NADPH] 1 (EC 1.1.1.184) (15-hydroxyprostaglandin dehydrogenase [NADP( )]) (EC 1.1.1.196) (EC 1.1.1.197) (20-beta-hydroxysteroid dehydrogenase)...»</title>
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		<updated>2021-05-12T15:08:59Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Carbonyl reductase [NADPH] 1 (EC 1.1.1.184) (15-hydroxyprostaglandin dehydrogenase [NADP( )]) (EC 1.1.1.196) (EC 1.1.1.197) (20-beta-hydroxysteroid dehydrogenase)...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Carbonyl reductase [NADPH] 1 (EC 1.1.1.184) (15-hydroxyprostaglandin dehydrogenase [NADP( )]) (EC 1.1.1.196) (EC 1.1.1.197) (20-beta-hydroxysteroid dehydrogenase) (NADPH-dependent carbonyl reductase 1) (Prostaglandin 9-ketoreductase) (PG-9-KR) (Prostaglandin-E(2) 9-reductase) (EC 1.1.1.189) (Short chain dehydrogenase/reductase family 21C member 1) [CBR] [CRN] [SDR21C1]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Age-related changes in hepatic activity and expression of detoxification enzymes in male rats.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23971034&lt;br /&gt;
|abstract=Process of aging is accompanied by changes in the biotransformation of xenobiotics and impairment of normal cellular functions by free radicals. Therefore, this study was designed to determine age-related differences in the activities and/or expressions of selected drug-metabolizing and antioxidant enzymes in young and old rats. Specific activities of 8 drug-metabolizing enzymes and 4 antioxidant enzymes were assessed in hepatic subcellular fractions of 6-week-old and 21-month-old male Wistar rats. Protein expressions of carbonyl reductase 1 ([[CBR1]]) and glutathione S-transferase (GST) were determined using immunoblotting. Remarkable age-related decrease in specific activities of CYP2B, CYP3A, and UDP-glucuronosyl transferase was observed, whereas no changes in activities of [[CYP1A2]], flavine monooxygenase, aldo-keto reductase 1C, and antioxidant enzymes with advancing age were found. On the other hand, specific activity of [[CBR1]] and GST was 2.4 folds and 5.6 folds higher in the senescent rats compared with the young ones, respectively. Interindividual variability in [[CBR1]] activity increased significantly with rising age. We suppose that elevated activities of GST and [[CBR1]] may protect senescent rats against xenobiotic as well as eobiotic electrophiles and reactive carbonyls, but they may alter metabolism of drugs, which are [[CBR1]] and especially GSTs substrates. &lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Antioxidants&lt;br /&gt;
* Enzyme Activation&lt;br /&gt;
* Inactivation, Metabolic&lt;br /&gt;
* Liver&lt;br /&gt;
* Male&lt;br /&gt;
* Metabolic Clearance Rate&lt;br /&gt;
* Oxidoreductases&lt;br /&gt;
* Pharmaceutical Preparations&lt;br /&gt;
* Rats&lt;br /&gt;
* Rats, Wistar&lt;br /&gt;
* Xenobiotics&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736498&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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