Enterostatin and its target mechanisms during regulation of fat intake

PHYSIOLOGY & BEHAVIOR

卷:83

Article; Proceedings Paper

Berger, K ; Winzell, MS ; Mei, J ; Erlanson-Albertsson, C

关键词: F1F0-ATP synthase;    beta-casomorphin;    two-phase partition;    brain membranes;    food intake;    opioid pathway;   

DOI  :  10.1016/j.physbeh.2004.08.040

来源: Elsevier

【 摘 要 】

A high-fat diet easily promotes hyperphagia giving an impression of an uncontrolled process. Fat digestion itself however provides control of fat intake through the digestion itself, carried out by pancreatic lipase and its protein cofactor colipase, and through enterostatin, a peptide released from procolipase during fat digestion. Procolipase (-/-) knockout mice have a severely reduced fat digestion and fat uptake, pointing to a major role of the digestive process itself. With a normal fat digestion, enterostatin basically restricts fat intake by preventing the overconsumption of fat. The mechanism for enterostatin might be an inhibition of a mu-opioid-mediated pathway, demonstrated through binding studies on SK-N-MC-cells and crude brain membranes. Another target protein of enterostatin is the beta-subunit of F1F0-ATPase, displaying a distinct binding of enterostatin, established through an aqueous two-phase partition system. The binding of enterostatin to F-1-ATPase was partially displaced by beta-casomorphin, a peptide stimulating fat intake and acting competitively to enterostatin. We frame a hypothesis that regulation of fat intake through enterostatin contains a reward component, which is an F-1-ATPase-mediated pathway, possibly complemented with an opioidergic pathway. (C) 2004 Elsevier Inc. All rights reserved.

【 授权许可】

Free