The proposed studies will characterize prostatic nitric oxide an explore its potential role in prostatic function. Because of its properties as a neurotransmitter, messenger molecule, vasodilator and cytotoxic agent, nitric oxide and its synthetic enzyme nitric oxide synthase may plan a significant yet diverse role in modulating prostatic function and development. Similar to its actions as a neurotransmitter in the central nervous system, nitric oxide may influence prostatic function through mechanisms attributed earlier to adrenergic, cholinergic and non-adrenergic non-cholinergic neuronal systems. Alternatively, nitric oxide may relax prostatic smooth muscle in a manner similar to alpha-adrenergic blockers used in the treatment of BPH. Finally, because it can induce cell death in a variety of tissues, nitric oxide may play a role in the control of prostate development, in the involution of the gland following androgen ablation, or in the development of BPH. To better understand the role of nitric oxide and nitric oxide synthase in the prostate we propose: 1) to characterize prostatic NOS in the rat and in a canine model for benign prostatic hyperplasia (BPH); 2) to examine the androgen regulation of NOS within the rat prostate; 3) to determine whether NOS co-localizes with neuroendocrine cells within the prostate; 4) to test the hypothesis that NO may be involved in castration-induced prostatic involution; and 5) to examine the role of NO in prostatic secretory function and in prostatic smooth muscle relaxation. The information acquired in these studies will provide new insight into the physiology of the prostate and may have profound implications regarding athe development of new approaches to the treatment of BPH.

Project Start
Project End
Budget Start
Budget End
Support Year
19
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Chon, J K; Borkowski, A; Partin, A W et al. (1999) Alpha 1-adrenoceptor antagonists terazosin and doxazosin induce prostate apoptosis without affecting cell proliferation in patients with benign prostatic hyperplasia. J Urol 161:2002-8
Crone, J K; Burnett, A L; Chamness, S L et al. (1998) Neuronal nitric oxide synthase in the canine prostate: aging, sex steroid, and pathology correlations. J Androl 19:358-64
Jarrard, D F; Paul, R; van Bokhoven, A et al. (1997) P-Cadherin is a basal cell-specific epithelial marker that is not expressed in prostate cancer. Clin Cancer Res 3:2121-8
Barrack, E R (1997) TGF beta in prostate cancer: a growth inhibitor that can enhance tumorigenicity. Prostate 31:61-70
Morton Jr, R A; Watkins, J J; Bova, G S et al. (1996) Hypermethylation of chromosome 17P locus D17S5 in human prostate tissue. J Urol 156:512-6
Epner, D E; Coffey, D S (1996) There are multiple forms of glyceraldehyde-3-phosphate dehydrogenase in prostate cancer cells and normal prostate tissue. Prostate 28:372-8
McEntee, M F; Epstein, J I; Syring, R et al. (1996) Characterization of prostatic basal cell hyperplasia and neoplasia in aged macaques: comparative pathology in human and nonhuman primates. Prostate 29:51-9
Sommerfeld, H J; Meeker, A K; Piatyszek, M A et al. (1996) Telomerase activity: a prevalent marker of malignant human prostate tissue. Cancer Res 56:218-22
Burnett, A L; Saito, S; Maguire, M P et al. (1995) Localization of nitric oxide synthase in spinal nuclei innervating pelvic ganglia. J Urol 153:212-7
Chamness, S L; Ricker, D D; Crone, J K et al. (1995) The effect of androgen on nitric oxide synthase in the male reproductive tract of the rat. Fertil Steril 63:1101-7

Showing the most recent 10 out of 23 publications