Literature DB >> 2829991

Pro-opiomelanocortin-derived peptides (ACTH/beta-endorphin/alpha-MSH) in brainstem baroreceptor areas of the rat.

M Palkovits1, E Mezey, R L Eskay.   

Abstract

Relatively high concentrations of adrenocorticotropic hormone (ACTH), beta-endorphin and alpha-melanocyte-stimulating hormone (alpha-MSH) were determined by radioimmunoassay in the nucleus of the solitary tract (NTS) of rats. Dense networks of immunoreactive fibers for these peptides were most prominent in the commissural part of the nucleus, where immunostained perikarya (8-15 per section) were also seen in colchicine-treated rats. Moderate peptide levels and moderately dense immunoreactive networks of these peptides were found in the lateral reticular nucleus (including the A1 and A5-C1 catecholaminergic cell groups) and the nucleus ambiguus. Ten different types of surgical lesions or transections were performed in the hypothalamus and the lower brainstem to determine the origin of ACTH, beta-endorphin and alpha-MSH in the brainstem baroreceptor centers. Except the commissural part of the NTS, the baroreceptor areas receive ACTH, beta-endorphin and alpha-MSH innervations from both the hypothalamic arcuate cells and local neurons in the NTS. Fibers in the commissural part of the NTS seem to be of local origin. Hypothalamic fibers to the rostral part of the NTS and the vasomotor A5-C1 cell groups descend in both a medial (through the periaqueductal central gray) and a lateral (ventrolateral tegmental fibers) pathway, whereas fibers to the caudal lateral reticular nucleus (A1 cell group) and the nucleus ambiguus may run only in the lateral pathway. The descending fibers may decussate somewhere in the caudal hypothalamus-rostral midbrain, but caudal to that level they run and terminate ipsilaterally. Fibers from the ACTH-, beta-endorphin- and alpha-MSH-containing cells in the NTS form a bundle arching between the NTS and the ventrolateral medulla and partially (40-55%) innervate the vasomotor and the vasodepressor areas, as well as the nucleus ambiguus.

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Year:  1987        PMID: 2829991     DOI: 10.1016/0006-8993(87)91676-3

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  32 in total

1.  Pro-opiomelanocortin gene transfer to the nucleus of the solitary track but not arcuate nucleus ameliorates chronic diet-induced obesity.

Authors:  Y Zhang; E Rodrigues; Y X Gao; M King; K Y Cheng; B Erdös; N Tümer; C Carter; P J Scarpace
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Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-07-29       Impact factor: 6.237

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Review 4.  Hypothalamic regulatory pathways and potential obesity treatment targets.

Authors:  Erin E Jobst; Pablo J Enriori; Puspha Sinnayah; Michael A Cowley
Journal:  Endocrine       Date:  2006-02       Impact factor: 3.633

5.  Hindbrain leptin stimulation induces anorexia and hyperthermia mediated by hindbrain melanocortin receptors.

Authors:  Karolina P Skibicka; Harvey J Grill
Journal:  Endocrinology       Date:  2008-12-04       Impact factor: 4.736

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7.  Sympathetic response to insulin is mediated by melanocortin 3/4 receptors in the hypothalamic paraventricular nucleus.

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8.  Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity.

Authors:  D Zegers; S Beckers; R Hendrickx; J K Van Camp; V de Craemer; A Verrijken; K Van Hoorenbeeck; S L Verhulst; R P Rooman; K N Desager; G Massa; L F Van Gaal; W Van Hul
Journal:  Int J Obes (Lond)       Date:  2013-10-07       Impact factor: 5.095

9.  Microinjections of alpha-melanocyte stimulating hormone into the nucleus ambiguus of the rat elicit vagally mediated bradycardia.

Authors:  Vineet C Chitravanshi; Suresh Bhatt; Hreday N Sapru
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-03-18       Impact factor: 3.619

10.  Brainstem application of melanocortin receptor ligands produces long-lasting effects on feeding and body weight.

Authors:  H J Grill; A B Ginsberg; R J Seeley; J M Kaplan
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

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