Literature DB >> 22496363

Changes in glucose tolerance and leptin responsiveness of rats offered a choice of lard, sucrose, and chow.

Ruth B S Harris1, John W Apolzan.   

Abstract

Rats offered chow, lard, and 30% sucrose solution (choice) rapidly become obese. We tested metabolic disturbances in rats offered choice, chow+lard, or chow+30% sucrose solution [chow+liquid sucrose (LS)] and compared them with rats fed a composite 60% kcal fat, 7% sucrose diet [high-fat diet (HFD)], or a 10% kcal fat, 35% sucrose diet [low-fat diet (LFD)]. Choice rats had the highest energy intake, but HFD rats gained the most weight. After 23 days carcass fat was the same for choice, HFD, chow+lard, and chow+LS groups. Glucose clearance was the same for all groups during an intraperitoneal glucose tolerance test (GTT) on day 12, but fasting insulin was increased in choice, LFD fed, and chow+LS rats. By contrast, only choice and chow+LS rats were resistant to an intraperitoneal injection of 2 mg leptin/kg on day 17. In experiment 2 choice rats were insulin insensitive during an intraperitoneal GTT, but this was corrected in an oral GTT due to GLP-1 release. UCP-1 protein was increased in brown fat and inguinal white fat in choice rats, and this was associated with a significant increase in energy expenditure of choice rats during the dark period whether expenditure was expressed on a per animal or a metabolic body size basis. The increase in expenditure obviously was not great enough to prevent development of obesity. Further studies are required to determine the mechanistic basis of the rapid onset of leptin resistance in choice rats and how consumption of sucrose solution drives this process.

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Year:  2012        PMID: 22496363      PMCID: PMC3378343          DOI: 10.1152/ajpregu.00477.2011

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  67 in total

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  21 in total

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Authors:  Marissa Seamon; WonMo Ahn; Ai-Jun Li; Sue Ritter; Ruth B S Harris
Journal:  Am J Physiol Endocrinol Metab       Date:  2019-07-30       Impact factor: 4.310

2.  In vivo and in vitro evidence that chronic activation of the hexosamine biosynthetic pathway interferes with leptin-dependent STAT3 phosphorylation.

Authors:  Arthur D Zimmerman; Ruth B S Harris
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-01-07       Impact factor: 3.619

Review 3.  Dietary components in the development of leptin resistance.

Authors:  Joseph R Vasselli; Philip J Scarpace; Ruth B S Harris; William A Banks
Journal:  Adv Nutr       Date:  2013-03-01       Impact factor: 8.701

4.  Sulforaphane improves leptin responsiveness in high-fat high-sucrose diet-fed obese mice.

Authors:  Noha M Shawky; Lakshman Segar
Journal:  Eur J Pharmacol       Date:  2018-07-29       Impact factor: 4.432

5.  Rapid onset and reversal of peripheral and central leptin resistance in rats offered chow, sucrose solution, and lard.

Authors:  John W Apolzan; Ruth B S Harris
Journal:  Appetite       Date:  2012-09-26       Impact factor: 3.868

6.  Development of leptin resistance in sucrose drinking rats is associated with consuming carbohydrate-containing solutions and not calorie-free sweet solution.

Authors:  Ruth B S Harris
Journal:  Appetite       Date:  2018-10-11       Impact factor: 3.868

7.  An acute method to test leptin responsiveness in rats.

Authors:  Bhavna N Desai; Ruth B S Harris
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2014-03-26       Impact factor: 3.619

8.  Hexosamine biosynthetic pathway activity in leptin resistant sucrose-drinking rats.

Authors:  Ruth B S Harris; John W Apolzan
Journal:  Physiol Behav       Date:  2014-11-06

9.  Leptin-induced increase in body fat content of rats.

Authors:  Ruth B S Harris
Journal:  Am J Physiol Endocrinol Metab       Date:  2012-12-04       Impact factor: 4.310

10.  Blockade of the cerebral aqueduct in rats provides evidence of antagonistic leptin responses in the forebrain and hindbrain.

Authors:  Michael I Vaill; Bhavna N Desai; Ruth B S Harris
Journal:  Am J Physiol Endocrinol Metab       Date:  2013-12-17       Impact factor: 4.310

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