Between 10 and 20 million American men are impotent. Several disease states such as atherosclerosis and diabetes mellitus have a high prevalence of impotence. Hypertension, hypercholesterolemia, diabetes mellitus and cigarette smoking are among the risk factors which may contribute to penile erectile dysfunction. It is now realized that the state of tone of human corpus cavernosum (HCC) smooth muscle plays a major role in the hemodynamics of penile erection. Previous research has focused exclusively on the neurologic control of HCC smooth muscle tone. Preliminary work indicates that the endothelium lining the lacunar spaces may influence HCC smooth muscle tone. The overall aim of this proposal is to determine the physiological role of the vascular endothelium in the control of HCC smooth muscle tone. HCC endothelial cells (EC) have, for the first time, been isolated, cultured and partially characterized. This proposal intends to establish an in vitro model system, utilizing HCC EC in culture, to investigate the interactions between the endothelium, smooth muscle and nerves of HCC. It is proposed: a) To continue the characterization of HCC EC and HCC smooth muscle cells in culture. b) To investigate the stimuli (mechanical or chemical) which cause the release of prostaglandins (PGs) from HCC EC, and to determine if these PGs have a role in the control of HCC smooth muscle tone, either directly or by inhibition of adrenergic neurotransmission. c) To determine if HCC EC release endothelium derived relaxing factor (EDRF) in response to mechanical or chemical stimuli. d) To determine if HCC EC synthesize and release acetylcholine. The outcome of this work may establish, for the first time, the physiological role of the vascular endothelium in penile erection. It will also allow the recognition of specific pathophysiological mechanisms leading to impotence in systemic diseases, such as diabetes mellitus and atherosclerosis, affecting normal EC function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK040487-01
Application #
3240796
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1988-08-01
Project End
1991-07-31
Budget Start
1988-08-01
Budget End
1989-07-31
Support Year
1
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
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Moreland, R B; Goldstein, I; Traish, A (1998) Sildenafil, a novel inhibitor of phosphodiesterase type 5 in human corpus cavernosum smooth muscle cells. Life Sci 62:PL 309-18
Udelson, D; Nehra, A; Hatzichristou, D G et al. (1998) Engineering analysis of penile hemodynamic and structural-dynamic relationships: Part I--Clinical implications of penile tissue mechanical properties. Int J Impot Res 10:15-24
Udelson, D; Nehra, A; Hatzichristou, D G et al. (1998) Engineering analysis of penile hemodynamic and structural-dynamic relationships: Part II--Clinical implications of penile buckling. Int J Impot Res 10:25-35
Udelson, D; Nehra, A; Hatzichristou, D G et al. (1998) Engineering analysis of penile hemodynamic and structural-dynamic relationships: Part III--Clinical considerations of penile hemodynamic and rigidity erectile responses. Int J Impot Res 10:89-99
Gupta, S; Moreland, R B; Yang, S et al. (1998) The expression of functional postsynaptic alpha2-adrenoceptors in the corpus cavernosum smooth muscle. Br J Pharmacol 123:1237-45
Gupta, S; Salimpour, P; Saenz de Tejada, I et al. (1998) A possible mechanism for alteration of human erectile function by digoxin: inhibition of corpus cavernosum sodium/potassium adenosine triphosphatase activity. J Urol 159:1529-36
Park, K; Moreland, R B; Goldstein, I et al. (1998) Sildenafil inhibits phosphodiesterase type 5 in human clitoral corpus cavernosum smooth muscle. Biochem Biophys Res Commun 249:612-7
Mulhall, J P; Daller, M; Traish, A M et al. (1997) Intracavernosal forskolin: role in management of vasculogenic impotence resistant to standard 3-agent pharmacotherapy. J Urol 158:1752-8; discussion 1758-9

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