2019
DOI: 10.1089/jmf.2018.0019
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Cardiovascular Effect of Diosgenin in Ovariectomized Rats

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Cited by 9 publications
(4 citation statements)
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“…In a study, OVX rats treated 28‐days with diosgenin (50 mg/kg, p.o.) significantly reduced the malondialdehyde concentration, and increased glutathione, superoxide dismutase, and nitric oxide (De Silva Morais et al., 2019).…”
Section: Discussionmentioning
confidence: 99%
“…In a study, OVX rats treated 28‐days with diosgenin (50 mg/kg, p.o.) significantly reduced the malondialdehyde concentration, and increased glutathione, superoxide dismutase, and nitric oxide (De Silva Morais et al., 2019).…”
Section: Discussionmentioning
confidence: 99%
“…After 1 week of adaptive feeding, the rats were anesthetized in a gas anesthesia machine containing isoflurane. The SD rats then underwent bilateral oophorectomy . Specifically, at the beginning of the operation, the hair in the surgical area of the rat’s bilateral lower back was removed.…”
Section: Methodsmentioning
confidence: 99%
“…The SD rats then underwent bilateral oophorectomy. 27 Specifically, at the beginning of the operation, the hair in the surgical area of the rat's bilateral lower back was removed. After disinfection with iodophor, the skin and muscle tissue of the rat were incised longitudinally on both sides of the spine to expose the abdominal cavity.…”
Section: In Vitro and In Vivo Biosafety Evaluationmentioning
confidence: 99%
“…In addition, Chinese yam polysaccharides also have anti-hyperlipidemic activity and can significantly reduce LDL and TC levels [ 96 ]. Dioscin, diosgenin and pseudoprotodioscin are phytoestrogens that are structurally similar to estrogens, with antioxidant, anti-inflammatory, anti-adipogenic, and inhibitory effects on atherosclerosis associated with estrogen deficiency [ 97 , 98 , 110 ]. Dioscin was found to not only regulate lipid metabolic homeostasis, but also attenuate postmenopausal atherosclerosis in HFD and ovariectomy (HFD-OVX)-induced low-density lipoprotein receptor-deficient (LDLR-/-) mice by inhibiting oxidative stress, inflammation, and apoptosis in part dependent on the peroxisome proliferator-activated receptor-γ coactivator 1-α (PGC-1α)/estrogen receptor alpha (Erα) pathway [ 98 ].…”
Section: Prevention and Treatment Of Metabolic Diseasesmentioning
confidence: 99%