Receptor autoradiography of μ and δ opioid peptide receptors in spontaneously hypertensive rats
The receptor autoradiographic distribution of opioid peptide receptors in spontaneously hypertensive rats (SHR) was compared to that of Sprague-Dawley (SD) rats, using the highly selective μ and δ opioid receptor ligands, [ 3H]DAGO (Tyr-D-Ala-Gly-NMe-Phe-Gly-ol) and [ 3H]DPDPE ([D-Pen 2,D-Pen 5]enke...
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Published in | Peptides (New York, N.Y. : 1980) Vol. 12; no. 4; pp. 779 - 785 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.07.1991
Elsevier Science |
Subjects | |
Online Access | Get full text |
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Summary: | The receptor autoradiographic distribution of opioid peptide receptors in spontaneously hypertensive rats (SHR) was compared to that of Sprague-Dawley (SD) rats, using the highly selective μ and δ opioid receptor ligands, [
3H]DAGO (Tyr-D-Ala-Gly-NMe-Phe-Gly-ol) and [
3H]DPDPE ([D-Pen
2,D-Pen
5]enkephalin), respectively. Although the distribution of these binding sites was similar in both strains, SHR showed significantly higher binding densities of μ receptors in 16 of 27 areas examined. These included the patch and matrix components of the caudate-putamen (CPu), olfactory tubercle, endopiriform nucleus, anterior cingulate cortex, ventral tegmental area, lateroposteral thalamic nucleus and the ventral part of the dentate gyrus. In contrast, SHR had lower [
3H]DAGO binding sites in the CA1 of the hippocampus. Conversely, SHR showed higher binding densities of δ receptors in 7 of 20 areas examined, including the CPu, CA2 and CA3 areas of the hippocampus and the central grey. High-to-low lateromedial gradients of striatal δ receptors were observed in both strains. Because opioid peptides are known to participate in locomotive behavior in rodents and in the control of blood pressure, the present results support a role of opioid peptidergic systems in the manifestation of hyperactivity and hypertension observed in SHR. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0196-9781 1873-5169 |
DOI: | 10.1016/0196-9781(91)90133-A |