Literature DB >> 9213358

Chronic ICV enterostatin preferentially reduced fat intake and lowered body weight.

L Lin1, J Chen, D A York.   

Abstract

The pancreatic peptide enterostatin will acutely reduce fat intake in rats provided a choice of diets. Chronic ICV infusions of enterostatin suppress the intake of high fat diet. However, the effects of chronic ICV enterostatin on diet choice has not previously been studied. To investigate this, enterostatin (0.5 microgram/h) or artificial cerebrospinal fluid (CSF) was infused for 9 days into the lateral ventricle of rats adapted to a two-choice high-fat (HF) and low-fat (LF) diet regime. Enterostatin reduced intake of HF diet with the maximum depression at day 4, but there was no compensatory increase in LF intake. The body weight of enterostatin-infused rats declined. This was associated with a reduction in fat pad and liver weights compared to the CSF-infused control rats. Serum triglycerides and insulin were decreased and corticosterone was elevated in enterostatin-infused rats. The data show that enterostatin will chronically reduce fat intake and body weight and suggest that enterostatin may attenuate the appetite for fat.

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Year:  1997        PMID: 9213358     DOI: 10.1016/s0196-9781(97)00128-9

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  11 in total

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Authors:  Ling Lin; Miejung Park; David A York
Journal:  Peptides       Date:  2006-11-17       Impact factor: 3.750

2.  5-HT1B receptors modulate the feeding inhibitory effects of enterostatin.

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3.  Expression of neural markers of gustatory signaling are differentially altered by continuous and intermittent feeding patterns.

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4.  Different metabolic responses to central and peripheral injection of enterostatin.

Authors:  Ling Lin; Miejung Park; Matt Hulver; David A York
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2005-12-08       Impact factor: 3.619

5.  Sensitivity to the satiating effects of exendin 4 is decreased in obesity-prone Osborne-Mendel rats compared to obesity-resistant S5B/Pl rats.

Authors:  S D Primeaux; M J Barnes; H D Braymer; G A Bray
Journal:  Int J Obes (Lond)       Date:  2010-04-20       Impact factor: 5.095

6.  Enterostatin deficiency increases serum cholesterol but does not influence growth and food intake in mice.

Authors:  Rita Miller; Dymphna D'Agostino; Charlotte Erlanson-Albertsson; Mark E Lowe
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-07-21       Impact factor: 4.310

7.  Central administration of the RFamide peptides, QRFP-26 and QRFP-43, increases high fat food intake in rats.

Authors:  Stefany D Primeaux; Christine Blackmon; Maria J Barnes; H Douglas Braymer; George A Bray
Journal:  Peptides       Date:  2008-08-13       Impact factor: 3.750

8.  CD36 mRNA in the gastrointestinal tract is differentially regulated by dietary fat intake in obesity-prone and obesity-resistant rats.

Authors:  Stefany D Primeaux; H Douglas Braymer; George A Bray
Journal:  Dig Dis Sci       Date:  2012-08-23       Impact factor: 3.199

9.  Enterostatin inhibition of angiogenesis: possible role of pAMPK and vascular endothelial growth factor A (VEGF-A).

Authors:  M Park; J Lyons; H Oh; Y Yu; E A Woltering; F Greenway; D A York
Journal:  Int J Obes (Lond)       Date:  2008-02-26       Impact factor: 5.095

Review 10.  Obesity pharmacotherapy: current perspectives and future directions.

Authors:  Monika Misra
Journal:  Curr Cardiol Rev       Date:  2013-02-01
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