Literature DB >> 10098939

Differential distribution of endomorphin 1- and endomorphin 2-like immunoreactivities in the CNS of the rodent.

S Martin-Schild1, A A Gerall, A J Kastin, J E Zadina.   

Abstract

Endomorphins are endogenous peptides that have high affinity and selectivity for the mu-opiate receptor and potent analgesic activity. The distributions of endomorphin 1 (Tyr-Pro-Trp-Phe-NH2; EM1) and endomorphin 2 (Tyr-Pro-Phe-Phe-NH2; EM2) in the rat central nervous system were determined by immunocytochemistry with two antisera, each demonstrating clear preference for the target antigen. Perikarya expressing EM2-like immunoreactivity were present in the posterior hypothalamus, whereas those expressing EM1-like immunoreactivity were present in both the posterior hypothalamus and the nucleus of the solitary tract (NTS). EM1-like immunoreactivity was more widely and densely distributed throughout the brain than was EM2-like immunoreactivity, whereas EM2-like immunoreactivity was more prevalent in the spinal cord than was EM1-like immunoreactivity. The greatest density of EM1-like-immunoreactive fibers was detected in the parabrachial nucleus and the NTS, with notable staining in the septum, diagonal band, bed nucleus of the stria terminalis, organum vasculosum, nucleus of Meynert, paraventricular thalamic nucleus, posterior hypothalamic nucleus, periaqueductal gray, locus coeruleus, nucleus accumbens, and amygdala. The greatest density of EM2-like-immunoreactive fibers was detected in the superficial laminae of the spinal cord dorsal horn and the nucleus of the spinal trigeminal tract. The overall pattern of immunoreactivities was similar in rat, mouse, and guinea pig, but some differences were observed. In many but not in all locations, immunoreactive fibers were prominently present in regions in which mu receptors are reported to be concentrated. The neuroanatomical results suggest that endomorphins participate in modulating nociceptive and autonomic nervous system processes and responsiveness to stress.

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Year:  1999        PMID: 10098939

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  66 in total

1.  Mapping of reinforcing and analgesic effects of the mu opioid agonist endomorphin-1 in the ventral midbrain of the rat.

Authors:  Thomas C Jhou; Sheng-Ping Xu; Mary R Lee; Courtney L Gallen; Satoshi Ikemoto
Journal:  Psychopharmacology (Berl)       Date:  2012-06-06       Impact factor: 4.530

2.  Endomorphin analogues containing D-Pro2 discriminate different mu-opioid receptor mediated antinociception in mice.

Authors:  Shinobu Sakurada; Hiroyuki Watanabe; Takafumi Hayashi; Masayuki Yuhki; Tsutomu Fujimura; Kimie Murayama; Chikai Sakurada; Tsukasa Sakurada
Journal:  Br J Pharmacol       Date:  2002-12       Impact factor: 8.739

Review 3.  Visualizing activation of opioid circuits by internalization of G protein-coupled receptors.

Authors:  Kevin Sinchak; Paul Micevych
Journal:  Mol Neurobiol       Date:  2003-04       Impact factor: 5.590

4.  Endomorphins exit the brain by a saturable efflux system at the basolateral surface of cerebral endothelial cells.

Authors:  Aniko Somogyvari-Vigh; Abba J Kastin; Jie Liao; James E Zadina; Weihong Pan
Journal:  Exp Brain Res       Date:  2004-05       Impact factor: 1.972

5.  Paradoxical hyperalgesia induced by mu-opioid receptor agonist endomorphin-2, but not endomorphin-1, microinjected into the centromedial amygdala of the rat.

Authors:  Maia Terashvili; Hsiang-En Wu; Emma Schwasinger; Leon F Tseng
Journal:  Eur J Pharmacol       Date:  2006-10-17       Impact factor: 4.432

6.  Effects of morphine and endomorphins on the polysynaptic reflex in the isolated rat spinal cord.

Authors:  Pao-Luh Tao; Yong-Shang Lai; Lok-Hi Chow; Eagle Yi-Kung Huang
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2004-12-17       Impact factor: 3.000

7.  Substance P and opioid peptidergic innervation of the anterior eye segment of the rat: an immunohistochemical study.

Authors:  J Michael Selbach; Samia H Buschnack; Klaus-Peter Steuhl; Stephan Kremmer; Uta Muth-Selbach
Journal:  J Anat       Date:  2005-03       Impact factor: 2.610

8.  Rewarding and psychomotor stimulant effects of endomorphin-1: anteroposterior differences within the ventral tegmental area and lack of effect in nucleus accumbens.

Authors:  Abraham Zangen; Satoshi Ikemoto; James E Zadina; Roy A Wise
Journal:  J Neurosci       Date:  2002-08-15       Impact factor: 6.167

9.  Opioid receptors on bulbospinal respiratory neurons are not activated during neuronal depression by clinically relevant opioid concentrations.

Authors:  Astrid G Stucke; Edward J Zuperku; Antonio Sanchez; Mislav Tonkovic-Capin; Viseslav Tonkovic-Capin; Sanda Mustapic; Eckehard A Stuth
Journal:  J Neurophysiol       Date:  2008-09-24       Impact factor: 2.714

10.  Clinically relevant infusion rates of mu-opioid agonist remifentanil cause bradypnea in decerebrate dogs but not via direct effects in the pre-Bötzinger complex region.

Authors:  Sanda Mustapic; Tomislav Radocaj; Antonio Sanchez; Zoran Dogas; Astrid G Stucke; Francis A Hopp; Eckehard A E Stuth; Edward J Zuperku
Journal:  J Neurophysiol       Date:  2009-11-11       Impact factor: 2.714

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