scholarly journals Parathyroid Hormone-Related Protein in Rat Penis: Expression, Localization, and Effect on Cavernosal Pressure1

Endocrinology ◽  
1999 ◽  
Vol 140 (9) ◽  
pp. 4342-4350 ◽  
Author(s):  
Hervé Lang ◽  
Nicole Endlich ◽  
Véronique Lindner ◽  
Karlhans Endlich ◽  
Thierry Massfelder ◽  
...  

Abstract Although PTH-related protein-(1–36) [PTHrP-(1–36)] is known to be expressed in smooth muscle and to exert potent myorelaxant effects, its tonic effects on cavernosal smooth muscle has not yet been explored. Using the RT-PCR technique, the present study establishes that PTHrP messenger RNA is present in microdissected corpus cavernosa in the rat. In immunohistochemical studies using affinity-purified antibodies to middle regions of PTHrP, immunostaining was localized throughout the penile structures, including vessels, cavernosal smooth muscle, and trabecular fibroblasts. Strong immunostaining for PTHrP was also detected in the dorsal nerve bundles. In anesthetized rats, intracavernosally injected boluses of increasing doses of PTHrP-(1–36) (0.3–30 pmol in 100 μl saline) had little effect on intracavernosal pressure. However, they markedly potentiated the dilatory response to papaverine (8–800 nmol), increasing the papaverine-induced intracavernous pressure by 2.5-fold, close to the mean arterial pressure. In conclusion, the cavernosal expression of PTHrP messenger RNA, the distribution of immunoreactive PTHrP throughout the structuro-functional components of the erectile apparatus and its strong potentiating action on papaverine-induced cavernosal relaxation, collectively suggest that PTHrP participates in the control of cavernosal tone.

2013 ◽  
Vol 305 (3) ◽  
pp. F333-F342 ◽  
Author(s):  
Denis Raison ◽  
Catherine Coquard ◽  
Mazène Hochane ◽  
Jacques Steger ◽  
Thierry Massfelder ◽  
...  

Parathyroid hormone-related protein (PTHrP) belongs to vasoactive factors that regulate blood pressure and renal hemodynamics both by reducing vascular tone and raising renin release. PTHrP is expressed in systemic and renal vasculature. Here, we wanted to assess the contribution of vascular smooth muscle cell endogenous PTHrP to the regulation of cardiovascular and renal functions. We generated a mouse strain ( SMA-CreER T2/ PTHrP L2/L2 or premutant PTHrP SM−/−), which allows temporally controlled, smooth muscle-targeted PTHrP knockdown in adult mice. Tamoxifen treatment induced efficient recombination of PTHrP-floxed alleles and decreased PTHrP expression in vascular and visceral smooth muscle cells of PTHrP SM−/− mice. Blood pressure remained unchanged in PTHrP SM−/− mice, but plasma renin concentration and creatinine clearance were reduced. Renal hemodynamics were further analyzed during clearance measurements in anesthetized mice. Conditional knockdown of PTHrP decreased renal plasma flow and glomerular filtration rate with concomitant reduction in filtration fraction. Similar measurements were repeated during acute saline volume expansion. Saline volume expansion induced a rise in renal plasma flow and reduced filtration fraction; both were blunted in PTHrP SM−/− mice leading to impaired diuresis. These findings show that endogenous vascular smooth muscle PTHrP controls renal hemodynamics under basal conditions, and it is an essential factor in renal vasodilation elicited by saline volume expansion.


Circulation ◽  
2004 ◽  
Vol 110 (2) ◽  
pp. 177-185 ◽  
Author(s):  
Nathalie Fiaschi-Taesch ◽  
Karen K. Takane ◽  
Sophia Masters ◽  
Juan Carlos Lopez-Talavera ◽  
Andrew F. Stewart

2008 ◽  
Vol 198 (2) ◽  
pp. 264-271 ◽  
Author(s):  
Jose Luis Martin-Ventura ◽  
Luis Miguel Blanco-Colio ◽  
Cesar Aparicio ◽  
Luis Ortega ◽  
Pedro Esbrit ◽  
...  

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