Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 1993;21:185-194

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pascual, D. W.
Right arrow Articles by Oparil, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pascual, D. W.
Right arrow Articles by Oparil, S.

Hypertension, Vol 21, 185-194, Copyright © 1993 by American Heart Association


ARTICLES

Nitric oxide mediates immune dysfunction in the spontaneously hypertensive rat

DW Pascual, VH Pascual, KL Bost, JR McGhee and S Oparil
Department of Oral Biology, Baptist Medical Centers, Birmingham, Ala.

The immune system of the spontaneously hypertensive rat is dysfunctional compared with that of normotensive control strains. Previous studies from our laboratory have shown that immunodepression in the spontaneously hypertensive rat was mediated by macrophages. The current study examines the mechanism for the depressed proliferative responses to concanavalin A typically observed by splenic mononuclear cells of spontaneously hypertensive rats. We tested various inhibitors of known macrophage products responsible for suppressing lymphoid function. The nitric oxide synthetase inhibitor NG-monomethyl L- arginine produced dose-dependent derepression of the proliferative responses of splenic mononuclear cells to concanavalin A. In contrast, indomethacin and catalase exhibited only weak derepression of the proliferative responses. Subsequent analysis showed that splenic mononuclear cells from spontaneously hypertensive rats generated greater nitric oxide levels than cells from Wistar-Kyoto rats, and nitric oxide levels were reduced when the inhibitor was added to splenic mononuclear cell cultures from spontaneously hypertensive rats. We further demonstrated that L-arginine is required for the development of the depressed mitogen-induced proliferative responses in these cells. Addition of L-arginine in excess of 10 microM to cultures diminished cell proliferation and increased nitric oxide. Polyclonal antibodies to murine interferon gamma reduced nitric oxide accumulation by approximately 50%, suggesting that interferon gamma is partially responsible for enhancing nitric oxide production in mitogen-stimulated splenic mononuclear cell cultures from spontaneously hypertensive rats. Thus, this study provides evidence that the immune depression observed in the spontaneously hypertensive rat is nitric oxide dependent.


This article has been cited by other articles:


Home page
Toxicol PatholHome page
J. Zhang, E. H. Herman, D. G. Robertson, M. D. Reily, A. Knapton, H. V. Ratajczak, N. Rifai, R. Honchel, K. T. Blanchard, R. E. Stoll, et al.
Mechanisms and Biomarkers of Cardiovascular Injury Induced by Phosphodiesterase Inhibitor III SK&F 95654 in the Spontaneously Hypertensive Rat
Toxicol Pathol, February 1, 2006; 34(2): 152 - 163.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
D. W. Pascual, T. Trunkle, and J. Sura
Fimbriated Salmonella enterica Serovar Typhimurium Abates Initial Inflammatory Responses by Macrophages
Infect. Immun., August 1, 2002; 70(8): 4273 - 4281.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
J. Y.H. Chan, L.-L. Wang, K. L.H. Wu, and S. H.H. Chan
Reduced Functional Expression and Molecular Synthesis of Inducible Nitric Oxide Synthase in Rostral Ventrolateral Medulla of Spontaneously Hypertensive Rats
Circulation, October 2, 2001; 104(14): 1676 - 1681.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. Tsujikawa, J. Kiryu, K. Yamashiro, A. Nonaka, K. Nishijima, Y. Honda, and Y. Ogura
Interactions Between Blood Cells and Retinal Endothelium in Endotoxic Sepsis
Hypertension, August 1, 2000; 36(2): 250 - 258.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
B. Nowicki, J. Singhal, L. Fang, S. Nowicki, and C. Yallampalli
Inverse Relationship between Severity of Experimental Pyelonephritis and Nitric Oxide Production in C3H/HeJ Mice
Infect. Immun., May 1, 1999; 67(5): 2421 - 2427.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
D. T. Lysle and T. How
Endogenous Opioids Regulate the Expression of Inducible Nitric Oxide Synthase by Splenocytes
J. Pharmacol. Exp. Ther., February 1, 1999; 288(2): 502 - 508.
[Abstract] [Full Text]


Home page
HypertensionHome page
C. Bernard, R. Merval, B. Esposito, and A. Tedgui
Resistance to Endotoxin Shock in Spontaneously Hypertensive Rats
Hypertension, June 1, 1998; 31(6): 1350 - 1356.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
D. W. Pascual, M. Coste, P. N. Boyaka, H. Kiyono, and J. R. McGhee
Spontaneously hypertensive rat: cholera toxin converts suppression to immunity through a Th2 cell-IL-4 pathway
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 1997; 273(4): R1509 - R1518.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. F. Dominiczak and D. F. Bohr
Nitric Oxide and Its Putative Role in Hypertension
Hypertension, June 1, 1995; 25(6): 1202 - 1211.
[Full Text]


Home page
Arch SurgHome page
L. M. Napolitano and C. Campbell
Nitric Oxide Inhibition Normalizes Splenocyte Interleukin-10 Synthesis in Murine Thermal Injury
Arch Surg, December 1, 1994; 129(12): 1276 - 1283.
[Abstract] [PDF]