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Research ArticleArticle

Endogenous Opioids Regulate the Expression of Inducible Nitric Oxide Synthase by Splenocytes

Donald T. Lysle and Tam How
Journal of Pharmacology and Experimental Therapeutics February 1999, 288 (2) 502-508;
Donald T. Lysle
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Tam How
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Abstract

In the present study, we tested the hypothesis that lipopolysaccharide (LPS)-induced expression of nitric oxide synthase (iNOS) by splenocytes is modulated through the activation of endogenous opioids in the central nervous system. The initial studies determined the parameters of LPS-induced expression of iNOS by splenocytes. Rats were injected with LPS at doses of 0, 1, 10, 100, and 1000 μg/kg, and measures of both iNOS mRNA and protein showed a dose-dependent increase in expression. In a time course study, rats received 100 μg/kg LPS and were killed at 0, 2, 4, 8, and 16 h postinjection. Both iNOS mRNA and protein expression was detectable at the 2-h time point, with peak expression occurring at 8 h. To evaluate the involvement of endogenous opioids, the opioid receptor antagonist naltrexone was administered at 0, 0.1, 1, or 10 mg/kg s.c. in combination with LPS (100 μg/kg), with a second injection of naltrexone at the same dose 4 h after the injection of LPS. Naltrexone induced a pronounced dose-dependent reduction in iNOS mRNA and protein expression by splenocytes. The modulation of iNOS expression occurs via central opioid receptors as intracerebroventricular administration but not peripheral administration of N-methylnaltrexone, the quaternary form of naltrexone that does not readily cross the blood-brain barrier, reduced the expression of iNOS. For all of the manipulations, nitrite/nitrate levels in the plasma showed effects similar to those for iNOS mRNA and protein. Collectively, these findings indicate that central opioid receptors are involved in the in vivo regulation of splenic nitric oxide production.

Footnotes

  • Send reprint requests to: Donald T. Lysle, Ph.D, Department of Psychology, Davie Hall, CB#3270, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3270. E-mail: dlysle{at}isis.unc.edu

  • ↵1 This research was supported by National Institute on Drug Abuse Grants DA10167 and DA07481. D.T.L. is the recipient of a Research Scientist Development Award DA00334 from the National Institute on Drug Abuse.

  • Abbreviations:
    iNOS
    inducible nitric oxide synthase
    i.c.v.
    intracerebroventricular
    RT
    reverse transcription
    PCR
    polymerase chain reaction
    LPS
    lipopolysaccharide
    • Received March 17, 1998.
    • Accepted August 20, 1998.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 288 (2)
Journal of Pharmacology and Experimental Therapeutics
Vol. 288, Issue 2
1 Feb 1999
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Research ArticleArticle

Endogenous Opioids Regulate the Expression of Inducible Nitric Oxide Synthase by Splenocytes

Donald T. Lysle and Tam How
Journal of Pharmacology and Experimental Therapeutics February 1, 1999, 288 (2) 502-508;

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Research ArticleArticle

Endogenous Opioids Regulate the Expression of Inducible Nitric Oxide Synthase by Splenocytes

Donald T. Lysle and Tam How
Journal of Pharmacology and Experimental Therapeutics February 1, 1999, 288 (2) 502-508;
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