Literature DB >> 2330072

Sites in the brain at which cholecystokinin octapeptide (CCK-8) acts to suppress feeding in rats: a mapping study.

R R Schick1, G J Harty, T L Yaksh, V L Go.   

Abstract

In this study, an examination was made of the sites in the brain of the rat at which the injection of cholecystokinin octapeptide (CCK-8) would alter food intake. Rats fasted for 24 hr received intracerebral injections of CCK-8 (1 nmol) or an equal volume of saline (0.5 microliters), into various sites in the brain through permanently implanted stainless steel cannulae. After prior acclimatisation to individual plexiglass compartments, latency to feed, as well as consumption of food and water during 0-20, 20-40 and 40-60 min after the injection, were recorded. The available food was the standard rat pellets, to which the animal otherwise had constant daily access. With this paradigm, active sites at which CCK-8 suppressed feeding were defined as sites at which consumption of food for 0-20 min was reduced by 25% or more, or the latency to feed was increased by 3 min or more after the injection of CCK-8, as compared to the effect of the injection of saline, made at the same site. Such active sites were most densely distributed in the rostral diencephalon, e.g. hypothalamus, the medial pontine area and lateral medulla, in the vicinity of the nucleus tractus solitarii (NTS). By grouping data for injections according to histologically identified sites, statistical analysis of groups of injections confirmed that these three major areas of the brain were active with regard to the suppression of feeding by CCK-8. These data suggest that CCK may not only initiate satiety messages, as a circulating hormone at peripheral sites, but also participate in the conduction of such information to the target in the brain by serving as a neurotransmitter in the lateral medulla (e.g. NTS), medial pontine area (e.g. relay station between the NTS and hypothalamus) and the lateral hypothalamus, where local release of CCK-8 after stomach loading has been observed.

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Year:  1990        PMID: 2330072     DOI: 10.1016/0028-3908(90)90050-2

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  10 in total

1.  Circulating GLP-1 and CCK-8 reduce food intake by capsaicin-insensitive, nonvagal mechanisms.

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Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-10-26       Impact factor: 3.619

Review 2.  Fat sensing and metabolic syndrome.

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Review 3.  Peripheral neural targets in obesity.

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4.  A neurohistochemical blueprint for pain-induced loss of appetite.

Authors:  A Malick; M Jakubowski; J K Elmquist; C B Saper; R Burstein
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

5.  Characterization of the role of endogenous cholecystokinin on the activity of the paraventricular nucleus of the hypothalamus in rats.

Authors:  Victoria Cano; Laura Ezquerra; M Pilar Ramos; Mariano Ruiz-Gayo
Journal:  Br J Pharmacol       Date:  2003-09-29       Impact factor: 8.739

6.  Development of a class of selective cholecystokinin type B receptor antagonists having potent anxiolytic activity.

Authors:  J Hughes; P Boden; B Costall; A Domeney; E Kelly; D C Horwell; J C Hunter; R D Pinnock; G N Woodruff
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

7.  A tale of two circuits: CCKNTS neuron stimulation controls appetite and induces opposing motivational states by projections to distinct brain regions.

Authors:  Carolyn W Roman; Stephanie R Sloat; Richard D Palmiter
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8.  Genetically and functionally defined NTS to PBN brain circuits mediating anorexia.

Authors:  Carolyn W Roman; Victor A Derkach; Richard D Palmiter
Journal:  Nat Commun       Date:  2016-06-15       Impact factor: 14.919

9.  Intracellular interplay between cholecystokinin and leptin signalling for satiety control in rats.

Authors:  Hayato Koizumi; Shahid Mohammad; Tomoya Ozaki; Kiyokazu Muto; Nanami Matsuba; Juhyon Kim; Weihong Pan; Eri Morioka; Takatoshi Mochizuki; Masayuki Ikeda
Journal:  Sci Rep       Date:  2020-07-20       Impact factor: 4.379

10.  Generation of brain tumours in mice by Cre-mediated recombination of neural progenitors in situ with the tamoxifen metabolite endoxifen.

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Journal:  Dis Model Mech       Date:  2015-12-24       Impact factor: 5.758

  10 in total

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