HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

Am J Physiol Regul Integr Comp Physiol 292: R1158-R1164, 2007. First published November 9, 2006; doi:10.1152/ajpregu.00429.2006
0363-6119/07 $8.00

This Article Free upon publication Full Text Full Text (PDF) All Versions of this Article: 292/3/R1158    most recent 00429.2006v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via ISI Web of Science (2) Citing Articles via Google Scholar Google Scholar Articles by Zheng, H. Articles by Patel, K. P. Search for Related Content PubMed PubMed Citation Articles by Zheng, H. Articles by Patel, K. P.

NEUROHUMORAL CONTROL OF CARDIOVASCULAR FUNCTION

Lack of central nitric oxide triggers erectile dysfunction in diabetes

Departments of ¹Cellular and Integrative Physiology and ²Pharmacology, University of Nebraska Medical Center, Omaha, Nebraska

Submitted 19 June 2006 ; accepted in final form 8 November 2006

Erectile dysfunction is a serious and common complication of diabetes mellitus. The proposed mechanisms for erectile dysfunction in diabetes include central and autonomic neuropathy, endothelial dysfunction, and smooth muscle dysfunction. The paraventricular nucleus (PVN) of the hypothalamus is known to be involved in centrally mediated penile erection. This study was designed to examine the role of nitric oxide (NO) within the central nervous system component of the behavioral responses including erection in diabetic rats. N-methyl-D-aspartic acid (NMDA)-induced erection, yawning, and stretch through the PVN can be blocked by prior administration of NO synthase (NOS) blocker, L-NMMA, in freely moving, conscious male normal rats. Four weeks after streptozotocin (STZ) and vehicle injections, NMDA-induced erection, yawning, and stretch responses through the PVN are significantly blunted in diabetic rats compared with control rats. Examination of neuronal NOS (nNOS) protein by Western blot analysis indicated a reduced amount of nNOS protein in the PVN of rats with diabetes compared with control rats. Furthermore, restoring nNOS within the PVN by gene transfer using adenoviral transfection significantly restored the erectile and yawning responses to NMDA in diabetic rats. These data demonstrate that a blunted NO mechanism within the PVN may contribute to NMDA-induced erectile dysfunction observed in diabetes mellitus.

neuronal nitric oxide synthase; sexual dysfunction; behavioral responses

This article has been cited by other articles:

				K. Powers-Martin, J. K. Phillip, V. C. Biancardi, and J. E. Stern Heterogeneous distribution of basal cyclic guanosine monophosphate within distinct neuronal populations in the hypothalamic paraventricular nucleus Am J Physiol Regulatory Integrative Comp Physiol, October 1, 2008; 295(4): R1341 - R1350. [Abstract] [Full Text] [PDF]

				Highlights From The Literature Physiology, April 1, 2007; 22(2): 70 - 72. [Full Text] [PDF]