1. Chronic cocaine alters hemodynamics and leukocyte-endothelial interactions in rat mesenteric venules.
- Author
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Chang SL, Bersig J, Felix B, Fiala M, and House SD
- Subjects
- Animals, Cell Adhesion drug effects, DNA Primers chemistry, Enzyme-Linked Immunosorbent Assay, Intercellular Adhesion Molecule-1 genetics, Intercellular Adhesion Molecule-1 metabolism, Interleukin-1 blood, Interleukin-6 blood, Male, N-Formylmethionine Leucyl-Phenylalanine pharmacology, RNA, Messenger metabolism, Rats, Rats, Sprague-Dawley, Reverse Transcriptase Polymerase Chain Reaction, Tumor Necrosis Factor-alpha analysis, Vasculitis blood, Vasculitis chemically induced, Venules drug effects, Cocaine toxicity, Endothelium, Vascular metabolism, Hemodynamics drug effects, Leukocytes metabolism, Mesenteric Veins drug effects
- Abstract
We investigated the effects of chronic cocaine exposure on the microcirculation in the rat mesenteric venules under both non-inflammatory and FMLP-induced inflammatory conditions. Chronic cocaine significantly increased WBC rolling flux in both conditions, and potentiated FMLP-induced leukocyte-endothelial cell adhesion (LEA). In cocaine-treated animals, total WBC number increased by 91%, and the ratio of white blood cell to red blood cell velocity was significantly lower, while vessel diameter was unchanged. Chronic cocaine decreased serum levels of tumor necrosis factor alpha (TNF-alpha) and interleukin-6 (IL-6), but had no effect on interleukin-1 beta (IL-1beta). Expression of intercellular adhesion molecule-1 (ICAM-1) was increased in mesenteric venules following chronic cocaine exposure, and may be one of the mechanisms underlying enhancement of FMLP-induced LEA. The increase in WBC count, WBC flux and LEA, and the change in cell velocity seen in the cocaine-treated animals could cause a decrease in effective vessel diameter and a change in intravascular resistance, and may underlie the progressive vascular damage seen in chronic cocaine-abusing individuals.
- Published
- 2000
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