alisol-a-24-acetate and Disease-Models--Animal

alisol-a-24-acetate has been researched along with Disease-Models--Animal* in 2 studies

Other Studies

2 other study(ies) available for alisol-a-24-acetate and Disease-Models--Animal

ArticleYear
Alisol A 24-acetate ameliorates nonalcoholic steatohepatitis by inhibiting oxidative stress and stimulating autophagy through the AMPK/mTOR pathway.
    Chemico-biological interactions, 2018, Aug-01, Volume: 291

    Topics: Adenylate Kinase; Animals; Autophagy; Cell Line; Cholestenones; Choline; Diet; Disease Models, Animal; Humans; Liver; Male; Methionine; Mice, Inbred C57BL; Non-alcoholic Fatty Liver Disease; Oxidative Stress; Signal Transduction; TOR Serine-Threonine Kinases

2018
The Protective Effects of Alisol A 24-Acetate from Alisma canaliculatum on Ovariectomy Induced Bone Loss in Vivo.
    Molecules (Basel, Switzerland), 2016, Jan-09, Volume: 21, Issue:1

    Alisma canaliculatum is a herb commonly used in traditional Korean medicine, and has been shown in scientific studies to have antitumor, diuretic hepatoprotective, and antibacterial effects. Recently, the anti-osteoclastogenesis of alisol A 24-acetate from Alisma canaliculatum was investigated in vitro. However, the influence of alisol A 24-acetate on osteoporosis in animals has not been investigated. The present study was undertaken to investigate the anti-osteoporotic effect of alisol A 24-acetate on bone mass in ovariectomized (OVX) mice and to identify the mechanism responsible for its effects. OVX mice were treated daily with 0.5 or 2 μg/g of alisol A 24-acetate for a period of six weeks. It was found that these administrations significantly suppressed osteoporosis in OVX mice and improved bone morphometric parameters. The serum estradiol, bone alkaline phosphatase levels, regulatory T/Th17 cell numbers were significantly increased by alisol A 24-acetate as compared with untreated OVX mice. In addition, TRAP activity was inhibited by alisol A 24-acetate in OVX mice. These results suggest alisol A 24-acetate effectively prevents bone loss in OVX mice, and that it can be considered a potential therapeutic for the treatment of postmenopausal osteoporosis.

    Topics: Acid Phosphatase; Alisma; Alkaline Phosphatase; Animals; Bone Density; Bone Density Conservation Agents; Bone Resorption; Cholestenones; Disease Models, Animal; Estradiol; Female; Femur; Humans; Isoenzymes; Lymphocyte Count; Mice; Mice, Inbred C3H; Osteoporosis, Postmenopausal; Ovariectomy; Phytotherapy; Plant Extracts; T-Lymphocytes, Regulatory; Tartrate-Resistant Acid Phosphatase; Th17 Cells

2016