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	<title>Translations:Niacin/49/en - Revision history</title>
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	<updated>2026-11-12T19:30:52Z</updated>
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		<title>FuzzyBot: Importing a new version from external source</title>
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		<summary type="html">&lt;p&gt;Importing a new version from external source&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Niacin and nicotinamide are both converted into the [[coenzyme]] NAD. NAD converts to NADP by phosphorylation in the presence of the enzyme [[NAD+ kinase]].  High energy requirements (brain) or high turnover rate (gut, skin) organs are usually the most susceptible to their deficiency. In the liver, niacinamide is converted to storage [[nicotinamide adenine dinucleotide]] (NAD). As needed, liver NAD is hydrolyzed to niacinamide and niacin for transport to tissues, there reconverted to NAD to serve as an enzyme cofactor. Excess niacin is methylated in the liver to N&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;-methylnicotinamide (NMN) and excreted in urine as such or as the oxidized metabolite [[N1-Methyl-2-pyridone-5-carboxamide|N&amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;-methyl-2-pyridone-5-carboxamide]] (2-pyridone). Decreased urinary content of these metabolites is a measure of niacin deficiency.&lt;br /&gt;
[[Image:Tryptophan metabolism.svg|thumb|300px|Niacin, [[serotonin]] (5-hydroxytryptamine), and [[melatonin]] [[biosynthesis]] from [[tryptophan]]]]&lt;/div&gt;</summary>
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