2022
DOI: 10.1016/j.sajb.2021.10.029
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Amaranthus hybridus Linn. leaf extract ameliorates oxidative stress and hepatic damage abnormalities induced by thioacetamide in rats

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Cited by 14 publications
(5 citation statements)
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“…The result reported for zinc and iron in the seed oil for this study was lower than the value reported for these minerals in the seed flour of M. flagellipes (32.60 ± 0.14 and 6.40 ± 0.03 mg/100g respectively) [40] and leaves (57.08 ± 8.44 and 5.83 ± 3.14 respectively) as reported by Ihedioha and Okoye [13]. This difference can be attributed to various factors ranging from the source of minerals to planting season, soil type, climate, and genetic and environmental factors [41][42]. Sickle cell anemia has been linked with zinc deficiency, making zinc supplementation in the diet helpful to manage or prevent some clinical manifestations [43].…”
Section: Discussionmentioning
confidence: 77%
“…The result reported for zinc and iron in the seed oil for this study was lower than the value reported for these minerals in the seed flour of M. flagellipes (32.60 ± 0.14 and 6.40 ± 0.03 mg/100g respectively) [40] and leaves (57.08 ± 8.44 and 5.83 ± 3.14 respectively) as reported by Ihedioha and Okoye [13]. This difference can be attributed to various factors ranging from the source of minerals to planting season, soil type, climate, and genetic and environmental factors [41][42]. Sickle cell anemia has been linked with zinc deficiency, making zinc supplementation in the diet helpful to manage or prevent some clinical manifestations [43].…”
Section: Discussionmentioning
confidence: 77%
“…TAA is a powerful hepato- and nephrotoxic agent that is widely used to establish a reproducible model of acute liver and kidney injury [ 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 ]. OA is a penta-cyclic triterpene that exists in free or glycosidic forms with one or more sugar moieties.…”
Section: Discussionmentioning
confidence: 99%
“…TAA produces a state of oxidative stress because of the formation of reactive unstable metabolites (TAA-S-oxide and TAA-S-dioxide), which enhance the ROS (reactive oxygen species) generation that promotes free radical-mediated damage to cellular components (e.g., DNA, proteins, and lipids) [ 1 , 7 ]. Additionally, the TAA metabolites covalent binding to antioxidant enzymes results in a repressed cellular antioxidant capacity in the liver and kidney and eventually leads to their injuries within 6 to 12 h after TAA incorporation [ 4 , 8 ]. Furthermore, TAA produces inflammation due to the augmentation of the expression of inflammatory cytokines such as IL-1β (interleukin-1β) and TNF-α (tumor-necrosis factor-alpha) [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…TAA is a potent hepatotoxic agent used widely to induce acute liver toxicity in an experimental rodent model by interfering in the nuclear transport of RNA from the nucleus to the cytoplasm and increases free radicals leading to membrane injury [27,28]. TAA is a potent hepatotoxicant and undergoes bioactivation to thioacetamide sulphoxide by microsomal enzyme CYP2E1 and thioacetamide-S, S-dioxide [28,29].…”
Section: Discussionmentioning
confidence: 99%