Mechanisms of CNS response to systemic immune challenge: the febrile response
- PMID: 9416669
- DOI: 10.1016/s0166-2236(97)01138-7
Mechanisms of CNS response to systemic immune challenge: the febrile response
Abstract
The acute-phase reaction is the multisystem response to acute inflammation. The central nervous system (CNS) mediates a coordinated set of autonomic, endocrine and behavioral responses that constitute the cerebral component of the acute-phase reaction. However, the mechanisms of immune signaling of the CNS remain controversial. Emerging evidence indicates that different parts of the acute-phase reaction are initiated by distinct mechanisms and in different brain regions. Cytokines produced as a result of local infections (for example, in the abdominal or thoracic cavities) might activate vagal sensory fibers, resulting in sickness behavior and fevers. Additionally, circulating immune stimuli might activate meningeal macrophages and perivascular microglia along the borders of the brain, eliciting the local production of prostaglandins and responses such as fever, anorexia, sleepiness, and activation of the hypothalamo-pituitary-adrenal (HPA) axis. The biological importance of these responses might favor the existence of multiple parallel CNS pathways that are engaged by cytokines.
Similar articles
-
Central nervous system recognition of peripheral inflammation: a neural, hormonal collaboration.Acta Biomed. 2007;78 Suppl 1:231-47. Acta Biomed. 2007. PMID: 17465337
-
Proinflammatory cytokines as pathogenetic mediators in the central nervous system: brain-periphery connections.Neuroimmunomodulation. 1995 Jan-Feb;2(1):2-15. doi: 10.1159/000096828. Neuroimmunomodulation. 1995. PMID: 7614256 Review.
-
Immune regulation within the central nervous system.J Neurol Sci. 1998 Apr 15;157(1):1-12. doi: 10.1016/s0022-510x(98)00049-5. J Neurol Sci. 1998. PMID: 9600670 Review.
-
Fever induction pathways: evidence from responses to systemic or local cytokine formation.Braz J Med Biol Res. 2001 Mar;34(3):301-14. doi: 10.1590/s0100-879x2001000300003. Braz J Med Biol Res. 2001. PMID: 11262580 Review.
-
[How does the immune system communicate with the brain?].Neurol Neurochir Pol. 1999 May-Jun;33(3):665-74; discussion 674-6. Neurol Neurochir Pol. 1999. PMID: 10540726 Review. Polish.
Cited by
-
Neural circuitry engaged by prostaglandins during the sickness syndrome.Nat Neurosci. 2012 Jul 26;15(8):1088-95. doi: 10.1038/nn.3159. Nat Neurosci. 2012. PMID: 22837039 Free PMC article. Review.
-
Effects of prostaglandin E2 on the electrical properties of thermally classified neurons in the ventromedial preoptic area of the rat hypothalamus.BMC Neurosci. 2005 Feb 27;6:14. doi: 10.1186/1471-2202-6-14. BMC Neurosci. 2005. PMID: 15733324 Free PMC article.
-
Lipopolysaccharide activates specific populations of hypothalamic and brainstem neurons that project to the spinal cord.J Neurosci. 2000 Sep 1;20(17):6578-86. doi: 10.1523/JNEUROSCI.20-17-06578.2000. J Neurosci. 2000. PMID: 10964963 Free PMC article.
-
The circumventricular organs participate in the immunopathogenesis of experimental autoimmune encephalomyelitis.Cerebrospinal Fluid Res. 2005 Sep 30;2:8. doi: 10.1186/1743-8454-2-8. Cerebrospinal Fluid Res. 2005. PMID: 16197544 Free PMC article.
-
Endogenous interleukin-10 is required for the defervescence of fever evoked by local lipopolysaccharide-induced and Staphylococcus aureus-induced inflammation in rats.J Physiol. 2003 Jun 1;549(Pt 2):653-64. doi: 10.1113/jphysiol.2002.037291. Epub 2003 Apr 11. J Physiol. 2003. PMID: 12692173 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical