Recent epidemiologic and clinical studies have affirmed the coexistence of erection and voiding disorders, such as erectile dysfunction and lower urinary tract symptoms, which indicates a true disease syndrome. The significance of this coexisting condition relates to its prevalence (as much as 20% of men) and impact (having quality-of-life ramifications and associations with other health co-morbidities). Coexisting erection and voiding disorders are also observed in sickle cell disease, which may offer a special paradigm to study and establish the science for their coexistence. Delineation of this link on scientific grounds would serve to develop needful, mechanism-specific interventions for coexistent erection and voiding disorders. In the sickle cell disease population, mounting scientific evidence has pointed to chronically defective function of nitric oxide, a major chemical regulator of biological processes in the body, as a fundamental factor for much of its various disease- related complications. Sickle cell disease offers a potentially informative paradigm by which to study and define dysregulated nitric oxide function as a likely determinant of concomitant erection and voiding disorders. Therefore, this research proposal is designed to investigate dysregulatory mechanisms of nitric oxide signaling of the lower genitourinary tract applying experimental biologic systems of nitric oxide signaling dysregulation and nitric oxide-based restorative interventions. The experimental plan will involve a combination of molecular, pharmacologic and physiologic techniques, using a genetically engineered sickle cell disease mouse model (which has been used advantageously for the study of erection disorders).
Specific aims are: (1) to evaluate lower urinary tract dysfunction in the sickle cell disease mouse as a possible progressive bladder failure phenotype; (2) to evaluate derangements of nitric oxide signaling in the lower genitourinary tract of the sickle cell disease mouse; (3) to evaluate whether transnitrosylation (a major protein interaction regulatory mechanism) of constitutive nitric oxide synthase regulates lower genitourinary tract function; and (4) to evaluate whether nitric oxide treatment attenuates lower genitourinary tract dysfunction.

Public Health Relevance

This project is relevant for public health since it addresses a condition that is highly prevalent and adversely affects basic health functions of daily life. Erection and urinary abnormalities occurring together are problematic to treat, although clarification of the science for this condition may lead to improved interventions if not preventions for it.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56DK114095-01A1
Application #
9761810
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Rankin, Tracy L
Project Start
2018-09-15
Project End
2019-08-31
Budget Start
2018-09-15
Budget End
2019-08-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Urology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205