Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2002-9-19
pubmed:abstractText
Vasoactive intestinal polypeptide (VIP) and pituitary adenylate cyclase-activating peptide (PACAP) are two closely related peptides that bind two homologous G protein-coupled receptors, VIP/PACAP receptor 1 (VPAC1R) and VIP/PACAP receptor II (VPAC2R), with equally high affinity. Recent reports suggest that VPAC2R plays a role in circadian rhythm and T cell functions. To further elucidate the functional activities of VPAC2R, we generated VPAC2R-deficient mice by deleting exons VIII-X of the VPAC2R gene. The VPAC2R-deficient mice showed retarded growth and had reduced serum IGF-I levels compared with gender-matched, wild-type siblings. The mutant mice appeared healthy and fertile at a young adult age. However, older male mutant mice exhibited diffuse seminiferous tubular degeneration with hypospermia and reduced fertility rate. The mutant mice appeared to have an increase in insulin sensitivity. VPAC2R-deficient mice had increased lean mass and decreased fat mass with reduced serum leptin levels. Indirect calorimetry experiments showed that the respiratory quotient values immediately following the transition into the dark cycle were significantly higher in male knockout mice for about 4 h. Additionally, male and female VPAC2R-deficient mice presented an increased basal metabolic rate (23% and 10%, respectively) compared with their wild-type siblings. Our results suggest that VPAC2R plays an important role in growth, basal energy expenditure, and male reproductive functions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0013-7227
pubmed:author
pubmed:issnType
Print
pubmed:volume
143
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3994-4006
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12239111-Amino Acid Sequence, pubmed-meshheading:12239111-Animals, pubmed-meshheading:12239111-Basal Metabolism, pubmed-meshheading:12239111-Body Composition, pubmed-meshheading:12239111-Female, pubmed-meshheading:12239111-Growth, pubmed-meshheading:12239111-Growth Disorders, pubmed-meshheading:12239111-Infertility, Male, pubmed-meshheading:12239111-Insulin, pubmed-meshheading:12239111-Insulin-Like Growth Factor I, pubmed-meshheading:12239111-Leptin, pubmed-meshheading:12239111-Male, pubmed-meshheading:12239111-Mice, pubmed-meshheading:12239111-Mice, Knockout, pubmed-meshheading:12239111-Molecular Sequence Data, pubmed-meshheading:12239111-Receptors, Vasoactive Intestinal Peptide, pubmed-meshheading:12239111-Receptors, Vasoactive Intestinal Peptide, Type II, pubmed-meshheading:12239111-Reference Values, pubmed-meshheading:12239111-Seminiferous Tubules, pubmed-meshheading:12239111-Sex Characteristics, pubmed-meshheading:12239111-Sperm Count
pubmed:year
2002
pubmed:articleTitle
Vasoactive intestinal polypeptide/pituitary adenylate cyclase-activating peptide receptor 2 deficiency in mice results in growth retardation and increased basal metabolic rate.
pubmed:affiliation
Division of Endocrine Research, Eli Lilly and Co., Indianapolis, Indiana 46285, USA.
pubmed:publicationType
Journal Article