Back to Search
Start Over
Real-time PCR analysis of leptin and leptin receptor expression in the rat prostate, and effects of leptin on prostatic acid phosphatase release
- Source :
- Scopus-Elsevier
- Publication Year :
- 2006
-
Abstract
- We have recently demonstrated the expression of leptin and leptin receptor (Ob-R) isoforms a, b, c, e and f in the rat seminal vesicles and prostate. The aim of the present study was to provide a semiquantitative real-time PCR estimation of leptin/Ob-R isoform mRNA expression in the seminal vesicles and individual components of rat prostate, and to ascertain the in vitro effects of leptin on prostate acid phosphatase release. The highest expression of the leptin and Ob-R genes was in the seminal vesicles and lateral prostate lobe, respectively. Of the various isoforms, Ob-Rb displayed the highest and Ob-Re the lowest expression. Leptin (10(-8) and 10(-6) M) enhanced acid phosphate release from seminal vesicles, and (10(-6) M) decreased it from the coagulating lobe. Taken together, our findings support the contention that leptin may be involved in the autocrine-paracrine functional regulation of rat seminal vesicles and prostate. The physiological relevance of the marked heterogeneity of the different prostate lobes in both their leptin/Ob-R expression and functional response to leptin remains to be addressed.
- Subjects :
- Gene isoform
Leptin
Male
medicine.medical_specialty
Acid Phosphatase
Gene Expression
Receptors, Cell Surface
Prostate
Internal medicine
Genetics
medicine
Animals
Protein Isoforms
RNA, Messenger
Receptor
Leptin receptor
biology
Reverse Transcriptase Polymerase Chain Reaction
digestive, oral, and skin physiology
Acid phosphatase
General Medicine
Recombinant Proteins
Rats
Real-time polymerase chain reaction
Endocrinology
medicine.anatomical_structure
Prostatic acid phosphatase
biology.protein
Receptors, Leptin
Protein Tyrosine Phosphatases
hormones, hormone substitutes, and hormone antagonists
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Scopus-Elsevier
- Accession number :
- edsair.doi.dedup.....13dc9466298c10bff75aad766673fdc3