Literature DB >> 3689429

Glucose kinetics during acute and chronic treatment of rats with 2[6(4-chloro-phenoxy)hexyl]oxirane-2-carboxylate, etomoxir.

Y T Kruszynska1, H S Sherratt.   

Abstract

(1) The effects of 2[6(4-chlorophenoxy)hexyl]oxirane-2-carboxylate (etomoxir), a candidate antiketonaemic and antidiabetic drug, on glucose turnover and recycling of glucose carbon in rats were determined using [3-3H, U-14C]glucose. (2) Etomoxir (Na salt) was infused continuously at a rate of 2 mg/hr in fasted male Wistar ab Boots rats (250-280 g) that had been maintained on a standard diet, or on a diet containing 0.1% of etomoxir for 10 days. (3) In rats treated acutely with etomoxir, plasma glucose concentrations were decreased by about 1 mM, glucose turnover was decreased by 14%, and recycling of glucose carbon by 30% compared with the controls infused with 0.14 M NaCl. (4) Infusion of etomoxir in rats chronically pretreated with etomoxir had little effect on plasma glucose concentrations, but increased glucose turnover and recycling of glucose carbon by 40%. (5) Acute infusion of etomoxir caused dramatic lowering of blood 3-hydroxybutyrate concentrations from 1 mM to about 0.03 mM with little change in other intermediary metabolites. (6) In rats chronically fed etomoxir, the proportion of pyruvate dehydrogenase in quadriceps muscle in the active form was 31% compared with 15% in the controls. (7) It was concluded that etomoxir in the acute dose given had only moderate effects on glucose turnover and that chronic administration of etomoxir caused increased glucose turnover and glucose recycling in the rat.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3689429     DOI: 10.1016/0006-2952(87)90458-8

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  10 in total

1.  Fatty acid metabolism-the first trigger for cachexia?

Authors:  David A Sassoon
Journal:  Nat Med       Date:  2016-06-07       Impact factor: 53.440

2.  Kinetic Analysis of Lipid Metabolism in Breast Cancer Cells via Nonlinear Optical Microscopy.

Authors:  Jue Hou; Nellone E Reid; Bruce J Tromberg; Eric O Potma
Journal:  Biophys J       Date:  2020-06-12       Impact factor: 4.033

3.  α1-Adrenergic receptors increase glucose oxidation under normal and ischemic conditions in adult mouse cardiomyocytes.

Authors:  Robert S Papay; Dianne M Perez
Journal:  J Recept Signal Transduct Res       Date:  2020-08-05       Impact factor: 2.092

4.  Targeting Fatty Acid Oxidation to Promote Anoikis and Inhibit Ovarian Cancer Progression.

Authors:  Brandon T Sawyer; Lubna Qamar; Tomomi M Yamamoto; Alexandra McMellen; Zachary L Watson; Jennifer K Richer; Kian Behbakht; Isabel R Schlaepfer; Benjamin G Bitler
Journal:  Mol Cancer Res       Date:  2020-03-20       Impact factor: 5.852

5.  Mercaptoacetate blocks fatty acid-induced GLP-1 secretion in male rats by directly antagonizing GPR40 fatty acid receptors.

Authors:  Ai-Jun Li; Qing Wang; Thu T Dinh; Steve M Simasko; Sue Ritter
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2016-01-20       Impact factor: 3.619

6.  Glucometabolic consequences of acute and prolonged inhibition of fatty acid oxidation.

Authors:  Anne-Marie Lundsgaard; Andreas M Fritzen; Trine S Nicolaisen; Christian S Carl; Kim A Sjøberg; Steffen H Raun; Anders B Klein; Eva Sanchez-Quant; Jakob Langer; Cathrine Ørskov; Christoffer Clemmensen; Matthias H Tschöp; Erik A Richter; Bente Kiens; Maximilian Kleinert
Journal:  J Lipid Res       Date:  2019-11-12       Impact factor: 5.922

7.  Autophagy-Dependent Generation of Free Fatty Acids Is Critical for Normal Neutrophil Differentiation.

Authors:  Thomas Riffelmacher; Alexander Clarke; Felix C Richter; Amanda Stranks; Sumeet Pandey; Sara Danielli; Philip Hublitz; Zhanru Yu; Errin Johnson; Tobias Schwerd; James McCullagh; Holm Uhlig; Sten Eirik W Jacobsen; Anna Katharina Simon
Journal:  Immunity       Date:  2017-09-12       Impact factor: 31.745

8.  Pharmacologic activation of peroxisome proliferator-activating receptor-α accelerates hepatic fatty acid oxidation in neonatal pigs.

Authors:  Kwanseob Shim; Sheila Jacobi; Jack Odle; Xi Lin
Journal:  Oncotarget       Date:  2018-05-08

9.  Multiomic analysis identifies CPT1A as a potential therapeutic target in platinum-refractory, high-grade serous ovarian cancer.

Authors:  Dongqing Huang; Shrabanti Chowdhury; Hong Wang; Sara R Savage; Richard G Ivey; Jacob J Kennedy; Jeffrey R Whiteaker; Chenwei Lin; Xiaonan Hou; Ann L Oberg; Melissa C Larson; Najmeh Eskandari; Davide A Delisi; Saverio Gentile; Catherine J Huntoon; Uliana J Voytovich; Zahra J Shire; Qing Yu; Steven P Gygi; Andrew N Hoofnagle; Zachary T Herbert; Travis D Lorentzen; Anna Calinawan; Larry M Karnitz; S John Weroha; Scott H Kaufmann; Bing Zhang; Pei Wang; Michael J Birrer; Amanda G Paulovich
Journal:  Cell Rep Med       Date:  2021-12-21

10.  Snail augments fatty acid oxidation by suppression of mitochondrial ACC2 during cancer progression.

Authors:  Ji Hye Yang; Nam Hee Kim; Jun Seop Yun; Eunae Sandra Cho; Yong Hoon Cha; Sue Bean Cho; Seon-Hyeong Lee; So Young Cha; Soo-Youl Kim; Jiwon Choi; Tin-Tin Manh Nguyen; Sunghyouk Park; Hyun Sil Kim; Jong In Yook
Journal:  Life Sci Alliance       Date:  2020-06-02
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.