Relevance of the nucleus of the solitary tract, gelatinous part, in learned preferences induced by intragastric nutrient administration

被引:4
作者
Zafra, Maria A. [1 ,2 ]
Aguera, Antonio D. [1 ]
Molina, Filomena [1 ,2 ]
Puerto, Amadeo [1 ,2 ]
机构
[1] Univ Granada, Dept Psychobiol, Campus Cartuja, E-18071 Granada, Spain
[2] Univ Granada, Mind Brain & Behav Res Ctr CIMCYC, Campus Cartuja, E-18071 Granada, Spain
关键词
Concurrent flavor learning; Predigested rewarding nutrients; Rapid visceral adjustments; NST dorsomedial region; Vagus-NST-LPBe axis; CONDITIONED TASTE-AVERSION; GASTRIC FOOD CONTENTS; C-FOS ACTIVATION; PARABRACHIAL NUCLEUS; BRAIN-STEM; ELECTRICAL-STIMULATION; GASTROINTESTINAL-TRACT; PARTIAL WITHDRAWAL; SMALL-INTESTINE; RAT-BRAIN;
D O I
10.1016/j.appet.2017.08.004
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Food preferences have been investigated in Wistar rats utilizing a learned concurrent flavor preference behavioral procedure. Previous studies have demonstrated that the perivagal administration of neurotoxin capsaicin disrupts the learning of preferences induced by intragastric administration of rewarding nutrients (pre-digested milk). The vagus nerve projects almost exclusively towards the nucleus of the solitary tract (NST), a brain medullary gateway for visceral signals. The objective of this study was to investigate the participation of the lateral portion of the dorsomedial region, the gelatinous subnucleus (SoIG), in the learning of a concurrent preference task. Results show that unlike neurologically intact animals, which learn this task correctly, animals lesioned in the gelatinous part of NST manifest a disruption of discrimination learning. Thus, intakes of the flavored stimulus paired with predigested liquid diet and of the flavored stimulus paired with physiological saline were virtually identical. However, SoIG- and sham-lesioned groups consumed similar total amounts of both flavors. These findings suggest that So1G, as a relay of the vagus nerve, along with its anatomical projection, the external lateral parabrachial subnucleus (LPBe), may constitute an anatomical axis that is important in the induction of concurrent flavor/side preferences. It also appears to be relevant in other behavioral processes that require rapid, processing of information from the upper gastrointestinal tract. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 96
页数:7
相关论文
共 82 条
[1]   Naloxone Impairs Concurrent but Not Sequential Flavor Aversion: Resorting to a Flexible/Explicit Learning [J].
Aguera, Antonio D. R. ;
Bernal, Antonio ;
Puerto, Amadeo .
BEHAVIORAL NEUROSCIENCE, 2016, 130 (01) :19-28
[2]   VISCEROTOPIC REPRESENTATION OF THE UPPER ALIMENTARY-TRACT IN THE RAT - SENSORY GANGLIA AND NUCLEI OF THE SOLITARY AND SPINAL TRIGEMINAL TRACTS [J].
ALTSCHULER, SM ;
BAO, X ;
BIEGER, D ;
HOPKINS, DA ;
MISELIS, RR .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 283 (02) :248-268
[3]   EFFECTS OF MEDULLARY AFFERENT VAGAL AXOTOMY AND AREA POSTREMA LESIONS ON SHORT-TERM AND LONG-TERM NACL-INDUCED TASTE-AVERSION LEARNING [J].
ARNEDO, M ;
GALLO, M ;
AGUERO, A ;
PUERTO, A .
PHYSIOLOGY & BEHAVIOR, 1990, 47 (06) :1067-1074
[4]   The role of vagal neurocircuits in the regulation of nausea and vomiting [J].
Babic, Tanja ;
Browning, Kirsteen N. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2014, 722 :38-47
[5]   PREFERENCE CONDITIONING BY CONCURRENT DIETS WITH DELAYED PROPORTIONAL REINFORCEMENT [J].
BAKER, BJ ;
BOOTH, DA .
PHYSIOLOGY & BEHAVIOR, 1989, 46 (04) :585-590
[6]   AN ATLAS OF THE RAT SUBPOSTREMAL NUCLEUS-TRACTUS-SOLITARIUS [J].
BARRACO, R ;
ELRIDI, M ;
ERGENE, E ;
PARIZON, M ;
BRADLEY, D .
BRAIN RESEARCH BULLETIN, 1992, 29 (06) :703-765
[7]  
BERTHOUD HR, 1995, ANAT EMBRYOL, V191, P203
[8]  
BLACKSHAW LA, 1987, J AUTONOM NERV SYST, V18, P225
[9]   Effect of vagal and splanchnic nerve section on Fos expression in ferret brain stem after emetic stimuli [J].
Boissonade, FM ;
Davison, JS .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1996, 271 (01) :R228-R236
[10]  
CLARKE GD, 1974, J PHYSIOL-LONDON, V239, pP41