TNF-α antagonist improves oxidative stress and lipid disorders induced by scorpion venom in the intestinal tissue

[Display omitted] •TNF-α antagonist improves intestinal oxidative damage induced by Aah venom.•TNF-α antagonist improves intestinal cytotoxicity in Aah-envenomed mice.•TNF-α antagonist improves postprandial serum lipid in Aah-envenomed mice.•TNF-α antagonist improves intestinal lipid profile in Aah-...

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Published inActa tropica Vol. 185; pp. 307 - 313
Main Authors Saidoune-Malek, Imane, Ait-Lounis, Aouatef, Laraba-Djebari, Fatima
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2018
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Abstract [Display omitted] •TNF-α antagonist improves intestinal oxidative damage induced by Aah venom.•TNF-α antagonist improves intestinal cytotoxicity in Aah-envenomed mice.•TNF-α antagonist improves postprandial serum lipid in Aah-envenomed mice.•TNF-α antagonist improves intestinal lipid profile in Aah-injected mice. We previously reported that Androctonus australis hector (Aah) venom induces inflammation in several tissues, however limited information is available on its role in gastrointestinal tract. Here we evaluate the involvement of TNF-α in lipid metabolism in the small intestine after Aah envenomation. To address these issues, NMRI mice (3-month-old) were pre-treated with a TNF-α antagonist, 30 min prior to Aah venom injection. Redox status, cytotoxicity and histopathological changes were analyzed in small intestine 3 and 24 h after Aah injection. Lipid metabolism was evaluated through lipid tolerance test in sera. Lipid content in small intestine was also evaluated at different times after envenomation. Obtained results showed that Aah venom affects the intestinal integrity. This cytotoxicity could be associated with lipid peroxidation and altered or insufficient antioxidant system. These results also highlight the perturbation of lipid absorption in intestine tissue of envenomed mice. The use of TNF-α antagonist prior to Aah venom injection seems to be able to improve lipid profile, oxidative stress and antioxidant activity. These findings suggest that Aah venom induces lipid alterations in the intestinal tissue mechanisms involving of TNF- α.
AbstractList We previously reported that Androctonus australis hector (Aah) venom induces inflammation in several tissues, however limited information is available on its role in gastrointestinal tract. Here we evaluate the involvement of TNF-α in lipid metabolism in the small intestine after Aah envenomation. To address these issues, NMRI mice (3-month-old) were pre-treated with a TNF-α antagonist, 30 min prior to Aah venom injection. Redox status, cytotoxicity and histopathological changes were analyzed in small intestine 3 and 24 h after Aah injection. Lipid metabolism was evaluated through lipid tolerance test in sera. Lipid content in small intestine was also evaluated at different times after envenomation. Obtained results showed that Aah venom affects the intestinal integrity. This cytotoxicity could be associated with lipid peroxidation and altered or insufficient antioxidant system. These results also highlight the perturbation of lipid absorption in intestine tissue of envenomed mice. The use of TNF-α antagonist prior to Aah venom injection seems to be able to improve lipid profile, oxidative stress and antioxidant activity. These findings suggest that Aah venom induces lipid alterations in the intestinal tissue mechanisms involving of TNF- α.
[Display omitted] •TNF-α antagonist improves intestinal oxidative damage induced by Aah venom.•TNF-α antagonist improves intestinal cytotoxicity in Aah-envenomed mice.•TNF-α antagonist improves postprandial serum lipid in Aah-envenomed mice.•TNF-α antagonist improves intestinal lipid profile in Aah-injected mice. We previously reported that Androctonus australis hector (Aah) venom induces inflammation in several tissues, however limited information is available on its role in gastrointestinal tract. Here we evaluate the involvement of TNF-α in lipid metabolism in the small intestine after Aah envenomation. To address these issues, NMRI mice (3-month-old) were pre-treated with a TNF-α antagonist, 30 min prior to Aah venom injection. Redox status, cytotoxicity and histopathological changes were analyzed in small intestine 3 and 24 h after Aah injection. Lipid metabolism was evaluated through lipid tolerance test in sera. Lipid content in small intestine was also evaluated at different times after envenomation. Obtained results showed that Aah venom affects the intestinal integrity. This cytotoxicity could be associated with lipid peroxidation and altered or insufficient antioxidant system. These results also highlight the perturbation of lipid absorption in intestine tissue of envenomed mice. The use of TNF-α antagonist prior to Aah venom injection seems to be able to improve lipid profile, oxidative stress and antioxidant activity. These findings suggest that Aah venom induces lipid alterations in the intestinal tissue mechanisms involving of TNF- α.
Author Saidoune-Malek, Imane
Ait-Lounis, Aouatef
Laraba-Djebari, Fatima
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  givenname: Imane
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/29909063$$D View this record in MEDLINE/PubMed
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Keywords Intestine tissue
Oxidative stress
Lipid metabolism
Aah venom
TNF-α antagonist
Language English
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Snippet [Display omitted] •TNF-α antagonist improves intestinal oxidative damage induced by Aah venom.•TNF-α antagonist improves intestinal cytotoxicity in...
We previously reported that Androctonus australis hector (Aah) venom induces inflammation in several tissues, however limited information is available on its...
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SubjectTerms Aah venom
Animals
Intestinal Mucosa - metabolism
Intestine tissue
Intestines - drug effects
Lipid metabolism
Lipid Metabolism - drug effects
Lipids - analysis
Mice
Mice, Inbred Strains
Oxidative stress
Oxidative Stress - drug effects
Scorpion Venoms - toxicity
TNF-α antagonist
Tumor Necrosis Factor-alpha - antagonists & inhibitors
Tumor Necrosis Factor-alpha - physiology
Title TNF-α antagonist improves oxidative stress and lipid disorders induced by scorpion venom in the intestinal tissue
URI https://dx.doi.org/10.1016/j.actatropica.2018.06.013
https://www.ncbi.nlm.nih.gov/pubmed/29909063
https://search.proquest.com/docview/2056759611
Volume 185
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