Effect of Canagliflozin, an SGLT2 Inhibitor, in Comparison with Atorvastatin on Dexamethasone-induced Hepatic Steatosis in Albino Rats

被引:3
|
作者
Ahmed, Eman, I [1 ,2 ]
Shaaban, Amany M. [3 ]
Latif, Abdel Karim M. Abdel [4 ]
机构
[1] Fayoum Univ, Fac Med, Pharmacol Dept, Al Fayyum, Egypt
[2] Jouf Univ, Coll Med, Dept Pharmacol & Therapeut, Sakakah, Egypt
[3] Fayoum Univ, Fac Sci, Chem Dept, Al Fayyum, Egypt
[4] Fayoum Univ, Fac Sci, Zool Dept, Al Fayyum, Egypt
关键词
Hepatic steatosis; canagliflozin; atorvastatin; dexamethasone; dyslipidemia; inhibitor; NONALCOHOLIC STEATOHEPATITIS; OXIDATIVE STRESS; LIVER-DAMAGE; EFFICACY; ASSAY; HYPERGLYCEMIA; CHOLESTEROL;
D O I
10.2174/1574885514666191007094424
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Non-Alcoholic Fatty Liver Disease (NAFLD) is a chronic liver disease that is considered to be the most common liver disease all over the world. It causes metabolic and hepatic damage that can progress to cirrhosis and hepatocellular carcinoma. Objective: Our research pointed to study the preventive effects of Canagliflozin (CANA) in comparison with Atorvastatin (ATO) as well as the combination of both on the development of experimental hepatic steatosis and dyslipidemia. Methods: Animals were grouped as control group; Dexamethasone (DEX) group; ATO/DEX treated group; CANA/DEX treated group and ATO+CANA/DEX treated group. Results: Significant elevations were observed in GSH, SOD and CAT activities, while highly significant decreases were observed in serum GOT, GPT, ALP, urea, blood glucose, CK-MB, LDH, T.G, T.C, MDA and P.C levels in the treated groups as compared to DEX group during experimental periods. Also, significant reductions in SGPT, SGOT, ALP, CK-MB, LDH, T.C and T.G levels were observed in CANA/DEX group as compared to ATO/DEX group. All these results were confirmed with histopathological findings where the severe damages and fatty degeneration in both kidney and liver tissues that developed by DEX administration were resolved by administration of ATO alone or in combination with CANA. Conclusion: These results indicate that CANA was as effective as ATO or a combination of both in reducing dyslipidemia and hepatic steatosis. The antioxidant and hypolipidemic effects of CANA may be responsible for the beneficial effects.
引用
收藏
页码:274 / 282
页数:9
相关论文
共 50 条
  • [11] Comparison of Dietary Control and Atorvastatin on High Fat Diet Induced Hepatic Steatosis and Hyperlipidemia in Rats
    Guiyuan Ji
    Xihong Zhao
    Liang Leng
    Peiyi Liu
    Zhuoqin Jiang
    Lipids in Health and Disease, 10
  • [12] Comparison of Dietary Control and Atorvastatin on High Fat Diet Induced Hepatic Steatosis and Hyperlipidemia in Rats
    Ji, Guiyuan
    Zhao, Xihong
    Leng, Liang
    Liu, Peiyi
    Jiang, Zhuoqin
    LIPIDS IN HEALTH AND DISEASE, 2011, 10
  • [13] The SGLT2 Inhibitor Canagliflozin Attenuates Fibrosis and Mitochondrial Dysfunction Induced by Hyperglycemia in Isolated Primary Human Cardiac Fibroblasts
    Varzideh, Fahimeh
    Jankauskas, Stanislovas
    Kansakar, Urna
    Lombardi, Angela
    Santulli, Gaetano
    CIRCULATION, 2023, 148
  • [14] Effects of canagliflozin, an SGLT2 inhibitor, on hepatic function in Japanese patients with type 2 diabetes mellitus: pooled and subgroup analyses of clinical trials
    Seko, Yuya
    Sumida, Yoshio
    Sasaki, Kazuyo
    Itoh, Yoshito
    Iijima, Hiroaki
    Hashimoto, Toshio
    Ishii, Shinichi
    Inagaki, Nobuya
    JOURNAL OF GASTROENTEROLOGY, 2018, 53 (01) : 140 - 151
  • [15] Effects of canagliflozin, an SGLT2 inhibitor, on hepatic function in Japanese patients with type 2 diabetes mellitus: pooled and subgroup analyses of clinical trials
    Yuya Seko
    Yoshio Sumida
    Kazuyo Sasaki
    Yoshito Itoh
    Hiroaki Iijima
    Toshio Hashimoto
    Shinichi Ishii
    Nobuya Inagaki
    Journal of Gastroenterology, 2018, 53 : 140 - 151
  • [16] Protective Effect of Bajakah Tampala (Spatholobus littoralis Hassk.) on Dexamethasone-Induced Renal Toxicity in Albino Rats
    Akmal, Tata Anfarul
    Dina, Cahya Farah
    Yudhana, Aditya
    Fikri, Faisal
    Purnomo, Agus
    Maslamama, Salipudin Tasil
    Purnama, Muhammad Thohawi Elziyad
    PAKISTAN VETERINARY JOURNAL, 2024, 44 (02) : 458 - 464
  • [17] DPP-4 Inhibitor and SGLT2 Inhibitor Additively Ameliorate Hepatic Steatosis in NAFLD Model Mice through Different Action Mechanisms
    Iwamoto, Yuichiro
    Kimura, Tomohiko
    Iwamoto, Hideyuki
    Fushimi, Yoshiro
    Sanada, Junpei
    Katakura, Yukino
    Shimoda, Masashi
    Mune, Tomoatsu
    Kaku, Kohei
    Kaneto, Hideaki
    DIABETES, 2023, 72
  • [18] Effects of the SGLT2 inhibitor ipragliflozin and metformin on hepatic steatosis and liver fibrosis: Sub-analysis of a randomized controlled study
    Hirayama, Kiichi
    Koshizaka, Masaya
    Ishibashi, Ryoichi
    Shoji, Mayumi
    Horikoshi, Takuro
    Sakurai, Kenichi
    Yokote, Koutaro
    PRIME V Study Grp
    DIABETES OBESITY & METABOLISM, 2025, 27 (04): : 2059 - 2069
  • [19] SGLT2 inhibitor as a potential therapeutic approach in hyperthyroidism-induced cardiopulmonary injury in rats
    Bastawy, Nermeen
    El-Mosallamy, Aliaa E. M. K.
    Aljuaydi, Samira H.
    AbuBakr, Huda O.
    Rasheed, Rabab Ahmed
    Sadek, A. S.
    Khattab, R. T.
    Abualyamin, Wael Botros
    Abdelaal, Shereen E.
    Boushra, Amy F.
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2024, 476 (07): : 1125 - 1143
  • [20] Effects of SGLT2 selective inhibitor ipragliflozin on hyperglycemia, hyperlipidemia, hepatic steatosis, oxidative stress, inflammation, and obesity in type 2 diabetic mice
    Tahara, Atsuo
    Kurosaki, Eiji
    Yokono, Masanori
    Yamajuku, Daisuke
    Kihara, Rumi
    Hayashizaki, Yuka
    Takasu, Toshiyuki
    Imamura, Masakazu
    Li, Qun
    Tomiyama, Hiroshi
    Kobayashi, Yoshinori
    Noda, Atsushi
    Sasamata, Masao
    Shibasaki, Masayuki
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2013, 715 (1-3) : 246 - 255