The Abilities of Salidroside on Ameliorating Inflammation, Skewing the Imbalanced Nucleotide Oligomerization Domain-Like Receptor Family Pyrin Domain Containing 3/Autophagy, and Maintaining Intestinal Barrier Are Profitable in Colitis
Identifieur interne : 000371 ( Main/Exploration ); précédent : 000370; suivant : 000372The Abilities of Salidroside on Ameliorating Inflammation, Skewing the Imbalanced Nucleotide Oligomerization Domain-Like Receptor Family Pyrin Domain Containing 3/Autophagy, and Maintaining Intestinal Barrier Are Profitable in Colitis
Auteurs : Jiuxi Liu ; Jiapei Cai ; Peng Fan ; Naisheng Zhang ; Yongguo CaoSource :
- Frontiers in Pharmacology [ 1663-9812 ] ; 2019.
Abstract
Salidroside (Sal), as a major glycoside extracted from
Url:
DOI: 10.3389/fphar.2019.01385
PubMed: 31849652
PubMed Central: 6901016
Affiliations:
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">The Abilities of Salidroside on Ameliorating Inflammation, Skewing the Imbalanced Nucleotide Oligomerization Domain-Like Receptor Family Pyrin Domain Containing 3/Autophagy, and Maintaining Intestinal Barrier Are Profitable in Colitis</title>
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<author><name sortKey="Cai, Jiapei" sort="Cai, Jiapei" uniqKey="Cai J" first="Jiapei" last="Cai">Jiapei Cai</name>
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<author><name sortKey="Zhang, Naisheng" sort="Zhang, Naisheng" uniqKey="Zhang N" first="Naisheng" last="Zhang">Naisheng Zhang</name>
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<author><name sortKey="Cao, Yongguo" sort="Cao, Yongguo" uniqKey="Cao Y" first="Yongguo" last="Cao">Yongguo Cao</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">The Abilities of Salidroside on Ameliorating Inflammation, Skewing the Imbalanced Nucleotide Oligomerization Domain-Like Receptor Family Pyrin Domain Containing 3/Autophagy, and Maintaining Intestinal Barrier Are Profitable in Colitis</title>
<author><name sortKey="Liu, Jiuxi" sort="Liu, Jiuxi" uniqKey="Liu J" first="Jiuxi" last="Liu">Jiuxi Liu</name>
</author>
<author><name sortKey="Cai, Jiapei" sort="Cai, Jiapei" uniqKey="Cai J" first="Jiapei" last="Cai">Jiapei Cai</name>
</author>
<author><name sortKey="Fan, Peng" sort="Fan, Peng" uniqKey="Fan P" first="Peng" last="Fan">Peng Fan</name>
</author>
<author><name sortKey="Zhang, Naisheng" sort="Zhang, Naisheng" uniqKey="Zhang N" first="Naisheng" last="Zhang">Naisheng Zhang</name>
</author>
<author><name sortKey="Cao, Yongguo" sort="Cao, Yongguo" uniqKey="Cao Y" first="Yongguo" last="Cao">Yongguo Cao</name>
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<series><title level="j">Frontiers in Pharmacology</title>
<idno type="eISSN">1663-9812</idno>
<imprint><date when="2019">2019</date>
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<front><div type="abstract" xml:lang="en"><p>Salidroside (Sal), as a major glycoside extracted from <italic>Rhodiola rosea</italic>
L., has exhibited its mighty anti-aging, anti-oxidant, anti-cancer, anti-inflammation, and neuroprotective effects in many diseases. Recently, it has showed its protective effect in colitis mice by activating the SIRT1/FoxOs pathway. Whereas, it is not known whether Sal has other protective mechanisms on dextran sulfate sodium (DSS)-induced colitis in mice. In this study, we investigated the protective effects and mechanisms of Sal on DSS-induced colitis in mice. The results demonstrated Sal was a competent candidate in the treatment of ulcerative colitis (UC). Sal remitted DSS-induced disease activity index (DAI), colon length shortening, and colonic pathological damage. Simultaneously, Sal alleviated excessive inflammation by reversing the IL-1β, TNF-α, and IL-10 protein levels in DSS-treated mice. Western blot analysis revealed that Sal inhibited p65 and p38 activation together with peroxisome proliferator-activated receptor (PPARγ) up-regulation. In addition, Sal skewed the imbalanced activation of nucleotide oligomerization domain-like receptor family pyrin domain containing 3 inflammasome and autophagy contributing to colitis recovery. The damaged intestinal barrier induced by DSS was also alleviated along with plasma lipopolysaccharides (LPS) reduction after Sal treatment. <italic>In vitro</italic>
, Sal showed PPARγ-dependent anti-inflammatory effect in LPS-stimulated RAW264.7 cells. In summary, our results demonstrated that Sal might be an effective factor for UC treatment and its pharmacological value deserved further development.</p>
</div>
</front>
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<tree><noCountry><name sortKey="Cai, Jiapei" sort="Cai, Jiapei" uniqKey="Cai J" first="Jiapei" last="Cai">Jiapei Cai</name>
<name sortKey="Cao, Yongguo" sort="Cao, Yongguo" uniqKey="Cao Y" first="Yongguo" last="Cao">Yongguo Cao</name>
<name sortKey="Fan, Peng" sort="Fan, Peng" uniqKey="Fan P" first="Peng" last="Fan">Peng Fan</name>
<name sortKey="Liu, Jiuxi" sort="Liu, Jiuxi" uniqKey="Liu J" first="Jiuxi" last="Liu">Jiuxi Liu</name>
<name sortKey="Zhang, Naisheng" sort="Zhang, Naisheng" uniqKey="Zhang N" first="Naisheng" last="Zhang">Naisheng Zhang</name>
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