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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=PARL</id>
	<title>PARL - История изменений</title>
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	<updated>2026-11-08T23:41:55Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=PARL&amp;diff=5545&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Presenilins-associated rhomboid-like protein, mitochondrial precursor (EC 3.4.21.105) (Mitochondrial intramembrane cleaving protease PARL) [Contains: P-beta (Pbet...»</title>
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		<updated>2021-05-12T13:49:08Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Presenilins-associated rhomboid-like protein, mitochondrial precursor (EC 3.4.21.105) (Mitochondrial intramembrane cleaving protease PARL) [Contains: P-beta (Pbet...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Presenilins-associated rhomboid-like protein, mitochondrial precursor (EC 3.4.21.105) (Mitochondrial intramembrane cleaving protease PARL) [Contains: P-beta (Pbeta)] [PSARL] [PRO2207]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Regulation of skeletal muscle oxidative capacity and insulin signaling by the mitochondrial rhomboid protease [[PARL]].&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/20444421&lt;br /&gt;
|abstract=Type 2 diabetes mellitus (T2DM) and aging are characterized by insulin resistance and impaired mitochondrial energetics. In lower organisms, remodeling by the protease pcp1 ([[PARL]] ortholog) maintains the function and lifecycle of mitochondria. We examined whether variation in [[PARL]] protein content is associated with mitochondrial abnormalities and insulin resistance. [[PARL]] mRNA and mitochondrial mass were both reduced in elderly subjects and in subjects with T2DM. Muscle knockdown of [[PARL]] in mice resulted in malformed mitochondrial cristae, lower mitochondrial content, decreased PGC1alpha protein levels, and impaired insulin signaling. Suppression of [[PARL]] protein in healthy myotubes lowered mitochondrial mass and insulin-stimulated glycogen synthesis and increased reactive oxygen species production. We propose that lower [[PARL]] expression may contribute to the mitochondrial abnormalities seen in aging and T2DM.&lt;br /&gt;
|mesh-terms=* Adolescent&lt;br /&gt;
* Adult&lt;br /&gt;
* Aged&lt;br /&gt;
* Aged, 80 and over&lt;br /&gt;
* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Cells, Cultured&lt;br /&gt;
* Diabetes Mellitus, Type 2&lt;br /&gt;
* Glycogen&lt;br /&gt;
* Humans&lt;br /&gt;
* Insulin&lt;br /&gt;
* Metalloproteases&lt;br /&gt;
* Mice&lt;br /&gt;
* Mice, Knockout&lt;br /&gt;
* Middle Aged&lt;br /&gt;
* Mitochondria&lt;br /&gt;
* Mitochondrial Proteins&lt;br /&gt;
* Muscle, Skeletal&lt;br /&gt;
* Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha&lt;br /&gt;
* Reactive Oxygen Species&lt;br /&gt;
* Signal Transduction&lt;br /&gt;
* Trans-Activators&lt;br /&gt;
* Transcription Factors&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835349&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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