Pharmacokinetics and feeding responses to muramyl dipeptide in rats

被引:13
作者
Fosset, S
Fromentin, G
Rampin, O
Lang, V
Mathieu, F
Tomé, D
机构
[1] INAPG, INRA, Unite Physiol Nutr & Comportement Alimentaire, F-75231 Paris, France
[2] Danone Vitapole, F-92350 Le Plessis Robinson, France
[3] INRA, AMIB, F-78352 Jouy En Josas, France
关键词
muramyl dipeptide; pharmacokinetics; meal pattern; food intake; anorexia; conditioned food aversion; behavioral satiety sequence;
D O I
10.1016/S0031-9384(03)00065-9
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
N-acetyl-muramyl-L-alanine-D-isoglutamine or muramyl dipeptide (MDP) is the minimally active subunit of bacterial peptidoglycan. During a systemic infection, the involvement of MDP has been demonstrated in food intake depression by the macrophage hydrolysis of Gram-positive bacteria. Under normal conditions, mammals are constantly exposed to the release of endogenous MDP from degraded gut flora and that of exogenous MDP from the diet. However, MDP digestion and absorption in the gastrointestinal tract are not fully understood, and their physiological significance needs to be clarified. After gavage (1.5 mg/kg), very low levels of MDP were found in the systemic circulation of rats and feeding patterns were not altered. In contrast, after the intraperitoneal injection of a similar dose, a depression in food intake was observed. The rats reduced their meal frequency and constant feeding rate, showing signs of satiety. The behavioral satiety sequence (BSS) was modified by behavioral changes, similar to those which appear during sickness, such as an increase in resting and a reduction in grooming. Our data suggest that the hypophagic effect of MDP may result from satiety and sickness behavior. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:173 / 182
页数:10
相关论文
共 54 条
[1]   The oligopeptide transporter (Pept-1) in human intestine: Biology and function [J].
Adibi, SA .
GASTROENTEROLOGY, 1997, 113 (01) :332-340
[2]   PHARMACOKINETICS AND METABOLISM OF MURAMYL DIPEPTIDE AND NOR-MURAMYL DIPEPTIDE [H-3-LABELED] IN THE MOUSE [J].
AMBLER, L ;
HUDSON, AM .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1984, 6 (02) :133-139
[3]   CHOLECYSTOKININ ELICITS COMPLETE BEHAVIORAL SEQUENCE OF SATIETY IN RATS [J].
ANTIN, J ;
GIBBS, J ;
HOLT, J ;
YOUNG, RC ;
SMITH, GP .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1975, 89 (07) :784-790
[4]   Control of IgE responses. V. Oral administration of a synthetic derivative of the inner bacterial cell wall (SDZ 280.636) to sensitized mice induces isotype specific suppression of peak hapten specific IgE antibody forming cell responses, serum IgE levels and immediate hypersensitivity responses. [J].
Auci, DL ;
Kleiner, GI ;
Chice, SM ;
Athanassiades, TJ ;
Dukor, P ;
Durkin, HG .
IMMUNOLOGICAL INVESTIGATIONS, 1998, 27 (1-2) :105-120
[5]   PEPTIDOGLYCAN FRAGMENTS DECREASE FOOD-INTAKE AND BODY-WEIGHT GAIN IN RATS [J].
BIBERSTINE, KJ ;
ROSENTHAL, RS .
INFECTION AND IMMUNITY, 1994, 62 (08) :3276-3281
[6]   BEHAVIORAL STRUCTURE AND MECHANISMS OF ANOREXIA - CALIBRATION OF NATURAL AND ABNORMAL INHIBITION OF EATING [J].
BLUNDELL, JE ;
ROGERS, PJ ;
HILL, AJ .
BRAIN RESEARCH BULLETIN, 1985, 15 (04) :371-376
[7]   MEAL PATTERN-ANALYSIS - ARTIFACTS, ASSUMPTIONS AND IMPLICATIONS [J].
CASTONGUAY, TW ;
KAISER, LL ;
STERN, JS .
BRAIN RESEARCH BULLETIN, 1986, 17 (03) :439-443
[8]   A MICROSTRUCTURAL ANALYSIS OF THE EFFECTS OF PRESATIATION ON FEEDING-BEHAVIOR IN THE RAT [J].
COOPER, SJ ;
FRANCIS, J .
PHYSIOLOGY & BEHAVIOR, 1993, 53 (02) :413-416
[9]   PRODUCTION OF LYMPHOCYTE ACTIVATING FACTOR IN THE ABSENCE OF ENDOGENOUS PYROGEN BY RABBIT OR HUMAN-LEUKOCYTES STIMULATED BY A MURAMYL DIPEPTIDE DERIVATIVE [J].
DAMAIS, C ;
RIVEAU, G ;
PARANT, M ;
GEROTA, J ;
CHEDID, L .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1982, 4 (05) :451-462
[10]   LITHIUM-CHLORIDE AND INESCAPABLE, UNSIGNALED TAIL SHOCK DIFFERENTIALLY AFFECT MEAL PATTERNS OF RATS [J].
DESS, NK ;
VANDERWEELE, DA .
PHYSIOLOGY & BEHAVIOR, 1994, 56 (01) :203-207