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      In vivo modulation of LPS-induced alterations in brain and peripheral cytokines and HPA axis activity by cannabinoids.

      Journal of Neuroimmunology
      Animals, Bornanes, pharmacology, Corticosterone, blood, Dronabinol, analogs & derivatives, Drug Interactions, Encephalitis, chemically induced, drug therapy, immunology, Hypothalamo-Hypophyseal System, drug effects, Interferon-gamma, Interleukin-10, Interleukin-1beta, Interleukin-6, Lipopolysaccharides, Lymphocyte Count, Male, Neuroimmunomodulation, Neuroprotective Agents, Piperidines, Pituitary-Adrenal System, Pyrazoles, Rats, Rats, Sprague-Dawley, Tumor Necrosis Factor-alpha

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          Abstract

          This study investigated cannabinoid receptor-mediated regulation of brain and peripheral cytokines in vivo. The cannabinoid receptor agonist, HU210 attenuated lipopolysaccharide (LPS)-induced increases in IL-1beta and TNFalpha in rat brain and IL-1beta, TNFalpha, IL-6 and IFNgamma in plasma. The CB(1) receptor antagonist, SR141716A, attenuated the immunosupressive effects of HU210 on IL-1beta, but not TNFalpha. SR141716A or the CB(2) receptor antagonist, SR144528, alone attenuated LPS-induced cytokine increases. LPS and/or cannabinoids also reduced circulating lymphocyte numbers and increased corticosterone levels. These data provide evidence for modulation of pro-inflammatory cytokines in vivo by cannabinoid receptors and inform the development of cannabinoids for neuroinflammatory disorders.

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