2022
DOI: 10.1007/s11033-022-07992-z
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Short-term trivalent arsenic and hexavalent chromium exposures induce gut dysbiosis and transcriptional alteration in adipose tissue of mice

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Cited by 7 publications
(2 citation statements)
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“…Arsenic exposure can also decrease PDE3b (phosphodiesterase 3b) expression and activity, an enzyme that regulates lipolysis and glucose uptake in adipocytes, resulting in hyperglycemia and insulin resistance [ 164 ]. In addition, SREBP (a transcription factor that regulates lipid metabolism) and PPARg (a nuclear receptor that regulates adipogenesis and glucose metabolism) have both been shown to be activated by iAs in adipocytes, resulting in increased expression of lipogenic genes and adipogenesis, eventually leading to the development of obesity, insulin resistance, and hyperglycemia [ 164 166 ].…”
Section: Diabetes and Arsenicmentioning
confidence: 99%
“…Arsenic exposure can also decrease PDE3b (phosphodiesterase 3b) expression and activity, an enzyme that regulates lipolysis and glucose uptake in adipocytes, resulting in hyperglycemia and insulin resistance [ 164 ]. In addition, SREBP (a transcription factor that regulates lipid metabolism) and PPARg (a nuclear receptor that regulates adipogenesis and glucose metabolism) have both been shown to be activated by iAs in adipocytes, resulting in increased expression of lipogenic genes and adipogenesis, eventually leading to the development of obesity, insulin resistance, and hyperglycemia [ 164 166 ].…”
Section: Diabetes and Arsenicmentioning
confidence: 99%
“…Correspondingly, in an in vitro study reduced brown adipogenesis and down-regulation of UCP1 expression significantly contribute to inhibition of thermogenesis upon As exposure [ 127 ]. In addition, As-induced alterations in gut microbiota including reduced relative abundance of Lactobacilli , Bifidobacteria , Akkermansia , Lachenospiraceae , Fecalibacterium , Eubacterium , and clostridium coccoid group with increased Enterobacteriaceae abundance may contribute to inhibition of adipogenesis, lipolysis, and thermogenesis in gonadal WAT, as well as increased adipogenesis and thermogenesis in BAT, as well as systemic inflammation [ 128 ]. It is also worth mentioning that Gong et al (2021) demonstrated transgenerational effect of paternal As exposure, characterized by reduced body adiposity in F2 offspring and increased susceptibility to diet-induced increase in body adiposity in F3 offspring [ 129 ].…”
Section: Introductionmentioning
confidence: 99%