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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ASMT</id>
	<title>ASMT - История изменений</title>
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	<updated>2026-06-11T02:19:40Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=ASMT&amp;diff=4445&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Acetylserotonin O-methyltransferase (EC 2.1.1.4) (Hydroxyindole O-methyltransferase) (HIOMT)  ==Publications==  {{medline-entry |title=The influence of ageing on...»</title>
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		<updated>2021-04-29T19:18:31Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Acetylserotonin O-methyltransferase (EC 2.1.1.4) (Hydroxyindole O-methyltransferase) (HIOMT)  ==Publications==  {{medline-entry |title=The influence of ageing on...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Acetylserotonin O-methyltransferase (EC 2.1.1.4) (Hydroxyindole O-methyltransferase) (HIOMT)&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=The influence of ageing on the extrapineal melatonin synthetic pathway.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29906492&lt;br /&gt;
|abstract=Ageing affects various physiological and metabolic processes in a body and a progressive accumulation of oxidative damage stands out as often used explanation. One of the most powerful scavenger of reactive oxygen species (ROS) in all organs is melatonin. A majority of melatonin supplied to the body via blood originates from the pineal gland. However, we have been interested in a locally produced melatonin. We have used 2.5- and 36-months-old Wistar rats. Tissues were collected and gene expression of AA-NAT and [[ASMT]], the two key enzymes in a synthesis of melatonin, was determined in brain, liver, kidney, heart, skin, and intestine. Since melatonin can influence antioxidant enzymes, the activity of superoxide dismutase (SOD) and catalase ([[CAT]]), and the level of GSH were measured in liver. In addition, Copper (Cu), Zinc (Zn), and Manganese (Mn) were also determined in liver since these microelements might affect the activity of antioxidant enzymes. The expression of AA-NAT and [[ASMT]] was increased in liver and skin of old animals. A positive correlation in AA-NAT and [[ASMT]] expression was observed in liver, intestine and kidney. Moreover, the activity of [[CAT]] enzyme in liver was increased while SOD activity was decreased. SOD and [[CAT]] were probably affected by the observed decreased amount of Cu, Zn, and Mn in liver of old animals. In our model, extrapineal melatonin pathway in ageing consisted of complex interplay of locally produced melatonin, activities of SOD and [[CAT]], and adequate presence of Cu, Zn and Mn microelements in order to defend organs against oxidative damage.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Antioxidants&lt;br /&gt;
* Catalase&lt;br /&gt;
* Copper&lt;br /&gt;
* Liver&lt;br /&gt;
* Melatonin&lt;br /&gt;
* Rats&lt;br /&gt;
* Rats, Wistar&lt;br /&gt;
* Reactive Oxygen Species&lt;br /&gt;
* Superoxide Dismutase&lt;br /&gt;
* Zinc&lt;br /&gt;
|keywords=* AA-NAT and ASMT&lt;br /&gt;
* Catalase&lt;br /&gt;
* Cu&lt;br /&gt;
* Mn&lt;br /&gt;
* SOD&lt;br /&gt;
* Zn&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.exger.2018.06.010&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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