Long-Term Exposure of Human Blood Vessels to HIV gp120, Morphine, and Anandamide Increases Endothelial Adhesion of Monocytes: Uncoupling of Nitric Oxide Release
Acute exposure of human saphenous vein or internal thoracic artery endothelium to either morphine [27.4 ± 3.7 and 35.4 ± 4.1 nM nitric oxide (NO), respectively] or anan-damide (18.3 ± 2.2 and 24.3 ± 3.0 nM, respectively) results in NO release, whereas exposure to the human immunodeficiency virus env...
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Published in: | Journal of cardiovascular pharmacology Vol. 31; no. 6; pp. 862 - 868 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Philadelphia, PA
Lippincott-Raven Publishers
01-06-1998
Hagerstown, MD Lippincott |
Subjects: | |
Online Access: | Get full text |
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Summary: | Acute exposure of human saphenous vein or internal thoracic artery endothelium to either morphine [27.4 ± 3.7 and 35.4 ± 4.1 nM nitric oxide (NO), respectively] or anan-damide (18.3 ± 2.2 and 24.3 ± 3.0 nM, respectively) results in NO release, whereas exposure to the human immunodeficiency virus envelope protein gp120 does not. After the short-term exposure of the vessel endothelium, monocyte adherence is diminished with morphine and anandamide treatment (jointly by −80%), whereas it is enhanced with that of gp120 (∼40%), indicating that gp120 enhances the ability of the endothelium to adhere monocytes. Long-term or continuous exposure of the endothelia to all agents results in a significant enhancement of monocyte adherence (p < 0.05), which is further increased when exposed to either morphine and anandamide plus gp120. This is caused by a desensitization of the endothelium to further NO release after the initial exposure to either anandamide or morphine. The results serve to indicate that in individuals abusing opiates and or cannabinoids, a tissue [i.e., central nervous system (CNS)] viral load may be higher, and acquired immunodeficiency syndrome (AIDS) may progress more rapidly because monocyte adherence and mobility is significantly increased, indicating a higher level of transmembrane migration. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0160-2446 1533-4023 |
DOI: | 10.1097/00005344-199806000-00009 |