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Neuropeptide W exerts a potent suppressive effect on blood leptin and insulin concentrations in the rat
Neuropeptide B/W receptor 1 (NPBWR1) and neuropeptide B/W receptor 2 (NPBWR2) are two structurally related orphan receptors linked to protein G. In rodents NPBWR2 is absent, and its counterpart is described as being similar to neuropeptide B/W receptor 2. Endogenous ligands of these receptors have b...
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Published in: | International journal of molecular medicine 2007-03, Vol.19 (3), p.401-405 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Neuropeptide B/W receptor 1 (NPBWR1) and neuropeptide B/W receptor 2 (NPBWR2)
are two structurally related orphan receptors linked to protein G. In rodents
NPBWR2 is absent, and its counterpart is described as being similar to neuropeptide
B/W receptor 2. Endogenous ligands of these receptors have been identified. One
of them is 29 amino acid residues long, uniquely modified with bromine and, thus,
termed neuropeptide B (NPB). The other, neuropeptide W (NPW), has been identified
in two molecular forms of 23 and 30 amino acids (NPW23 and NPW30), respectively.
Both NPB and NPW affect food intake and energy expenditure. Since leptin, a potent
anti-obesity hormone, and insulin are involved in the control of energy homeostasis,
the present study aimed to investigate whether NPB and NPW affect leptin and insulin
secretion in the rat. RT-PCR technique revealed the presence of ppNPB, ppNPW,
NPBWR1 and NPBWR2-like mRNAs in isolated pancreatic islets of the rat. NPB and
NPW immunoreactivities were observed in all of the cells of the pancreatic islets.
Only when a higher dose was administered (3 nmol/100 g body weight) did NPW transiently
lower blood insulin levels whereas NPB injection did not alter insulinaemia in
the studied rats. At 30 min, but not 60, of the experiment, NPW notably lowered
blood leptin concentrations at both tested doses. On the contrary, NPB injections
had no effect on blood leptin and insulin concentrations. Thus, the results suggest
that NPW but not NPB exerts a potent suppressive effect on blood leptin concentrations
in the rat, and this mechanism may be involved in NPW regulation of energy homeostasis. |
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ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.19.3.401 |