Matches in SemOpenAlex for { <https://semopenalex.org/work/W2897750223> ?p ?o ?g. }
- W2897750223 endingPage "1528" @default.
- W2897750223 startingPage "1516" @default.
- W2897750223 abstract "<b><i>Background/Aims:</i></b> Previous studies have shown that homocysteine (Hcy) is an important intestinal-derived uremic toxin. However, whether Hcy is involved in the epithelial barrier dysfunction observed in uremia remains unclear. This study aimed to investigate the effect of Hcy on intestinal permeability and intestinal barrier structure and function in adenine-induced uremic rats. <b><i>Methods:</i></b> Sprague-Dawley rats were divided into five groups: normal control (group NC), Hcy (group H), uremia (group U), uremia + Hcy (group UH), and uremia + Hcy + VSL#3 (group UHV). Experimental uremia was induced by intragastric adenine administration, and Hcy was injected subcutaneously. The animal models were assessed for renal function and pathological tissue staining. The pathological changes of intestinal tissue were observed by hematoxylin and eosin staining and electron microscopy. The serum and intestinal tissue levels of Hcy, interleukin (IL)-6, tumor necrosis factor (TNF)-α, superoxide dismutase (SOD), and malondialdehyde (MDA) as well as serum endotoxin and intestinal permeability were assessed. The levels of the tight junction proteins claudin-1, occludin, and zonula occludens-1 (ZO-1) were assessed by western blotting. <b><i>Results:</i></b> Blood analyses and renal pathology indicated that experimental uremia was induced successfully. Pathological damage to intestinal structure was most obvious in group UH. Serum and tissue Hcy, serum endotoxin, and intestinal permeability were significantly elevated in group UH. The protein levels of claudin-1, occludin, and ZO-1 were decreased to various degrees in group UH compared with groups NC, H, and U. The serum and tissue levels of IL-6, TNF-α, and MDA were significantly increased, while SOD activity was markedly decreased. Supplementation with the probiotic VSL#3 improved these parameters to various degrees and up-regulated the abundance of tight junction proteins, which indicated a role for Hcy in the increase of intestinal permeability and destruction of the epithelial barrier in uremia. <b><i>Conclusion:</i></b> Hcy aggravates the increase of intestinal permeability and destruction of the epithelial barrier by stimulating inflammatory and oxidative damage. Probiotic administration can ameliorate this damage by reducing the levels of Hcy-induced inflammation and oxidation." @default.
- W2897750223 created "2018-10-26" @default.
- W2897750223 creator A5002656825 @default.
- W2897750223 creator A5012784116 @default.
- W2897750223 creator A5029255037 @default.
- W2897750223 creator A5036726873 @default.
- W2897750223 creator A5066271821 @default.
- W2897750223 creator A5084658435 @default.
- W2897750223 creator A5087122988 @default.
- W2897750223 creator A5088170440 @default.
- W2897750223 creator A5088229449 @default.
- W2897750223 date "2018-01-01" @default.
- W2897750223 modified "2023-09-23" @default.
- W2897750223 title "Homocysteine Aggravates Intestinal Epithelial Barrier Dysfunction in Rats with Experimental Uremia" @default.
- W2897750223 cites W1568195207 @default.
- W2897750223 cites W1912108948 @default.
- W2897750223 cites W1968382122 @default.
- W2897750223 cites W1972567911 @default.
- W2897750223 cites W1983217656 @default.
- W2897750223 cites W2037703588 @default.
- W2897750223 cites W2042613045 @default.
- W2897750223 cites W2049099916 @default.
- W2897750223 cites W2062729328 @default.
- W2897750223 cites W2071790674 @default.
- W2897750223 cites W2074647034 @default.
- W2897750223 cites W2097001096 @default.
- W2897750223 cites W2105234132 @default.
- W2897750223 cites W2146648547 @default.
- W2897750223 cites W2147394461 @default.
- W2897750223 cites W2166329077 @default.
- W2897750223 cites W2187782277 @default.
- W2897750223 cites W2291733689 @default.
- W2897750223 cites W2412313238 @default.
- W2897750223 cites W2579583038 @default.
- W2897750223 cites W2612161536 @default.
- W2897750223 cites W2742337878 @default.
- W2897750223 cites W60937635 @default.
- W2897750223 doi "https://doi.org/10.1159/000494018" @default.
- W2897750223 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30336454" @default.
- W2897750223 hasPublicationYear "2018" @default.
- W2897750223 type Work @default.
- W2897750223 sameAs 2897750223 @default.
- W2897750223 citedByCount "13" @default.
- W2897750223 countsByYear W28977502232019 @default.
- W2897750223 countsByYear W28977502232020 @default.
- W2897750223 countsByYear W28977502232021 @default.
- W2897750223 countsByYear W28977502232022 @default.
- W2897750223 countsByYear W28977502232023 @default.
- W2897750223 crossrefType "journal-article" @default.
- W2897750223 hasAuthorship W2897750223A5002656825 @default.
- W2897750223 hasAuthorship W2897750223A5012784116 @default.
- W2897750223 hasAuthorship W2897750223A5029255037 @default.
- W2897750223 hasAuthorship W2897750223A5036726873 @default.
- W2897750223 hasAuthorship W2897750223A5066271821 @default.
- W2897750223 hasAuthorship W2897750223A5084658435 @default.
- W2897750223 hasAuthorship W2897750223A5087122988 @default.
- W2897750223 hasAuthorship W2897750223A5088170440 @default.
- W2897750223 hasAuthorship W2897750223A5088229449 @default.
- W2897750223 hasBestOaLocation W28977502231 @default.
- W2897750223 hasConcept C126322002 @default.
- W2897750223 hasConcept C134018914 @default.
- W2897750223 hasConcept C177779419 @default.
- W2897750223 hasConcept C185592680 @default.
- W2897750223 hasConcept C2775962179 @default.
- W2897750223 hasConcept C2776151105 @default.
- W2897750223 hasConcept C2776635150 @default.
- W2897750223 hasConcept C2777090595 @default.
- W2897750223 hasConcept C2778401633 @default.
- W2897750223 hasConcept C2781071285 @default.
- W2897750223 hasConcept C55493867 @default.
- W2897750223 hasConcept C71924100 @default.
- W2897750223 hasConceptScore W2897750223C126322002 @default.
- W2897750223 hasConceptScore W2897750223C134018914 @default.
- W2897750223 hasConceptScore W2897750223C177779419 @default.
- W2897750223 hasConceptScore W2897750223C185592680 @default.
- W2897750223 hasConceptScore W2897750223C2775962179 @default.
- W2897750223 hasConceptScore W2897750223C2776151105 @default.
- W2897750223 hasConceptScore W2897750223C2776635150 @default.
- W2897750223 hasConceptScore W2897750223C2777090595 @default.
- W2897750223 hasConceptScore W2897750223C2778401633 @default.
- W2897750223 hasConceptScore W2897750223C2781071285 @default.
- W2897750223 hasConceptScore W2897750223C55493867 @default.
- W2897750223 hasConceptScore W2897750223C71924100 @default.
- W2897750223 hasIssue "5" @default.
- W2897750223 hasLocation W28977502231 @default.
- W2897750223 hasLocation W28977502232 @default.
- W2897750223 hasLocation W28977502233 @default.
- W2897750223 hasOpenAccess W2897750223 @default.
- W2897750223 hasPrimaryLocation W28977502231 @default.
- W2897750223 hasRelatedWork W1969002939 @default.
- W2897750223 hasRelatedWork W1972216846 @default.
- W2897750223 hasRelatedWork W2003814064 @default.
- W2897750223 hasRelatedWork W2006996729 @default.
- W2897750223 hasRelatedWork W2007767297 @default.
- W2897750223 hasRelatedWork W2072979799 @default.
- W2897750223 hasRelatedWork W2075043838 @default.
- W2897750223 hasRelatedWork W2077277650 @default.
- W2897750223 hasRelatedWork W2079944499 @default.