Journal
INTERNATIONAL REVIEWS OF IMMUNOLOGY
Volume 35, Issue 5, Pages 415-433Publisher
TAYLOR & FRANCIS INC
DOI: 10.3109/08830185.2015.1127369
Keywords
acetylcholine; alpha7 nicotinic acetylcholine receptor; inflammation; sepsis; vagus nerve
Categories
Funding
- National Natural Science Foundation [81130035, 81372054, 81272090, 81121004]
- National Basic Research Program of China [2012CB518102]
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The vagus nerve can sense peripheral inflammation and transmit action potentials from the periphery to the brainstem. Vagal afferent signaling is integrated in the brainstem, and efferent vagus nerves carry outbound signals that terminate in spleen and other organs. Stimulation of efferent vagus nerve leads to the release of acetylcholine in these organs. In turn, acetylcholine interacts with members of the nicotinic acetylcholine receptor (nAChR) family, particularly with the alpha7 nicotinic acetylcholine receptor (alpha 7nAChR), which is expressed by macrophages and other cytokine-producing cells. Ultimately, the production of proinflammatory cytokines is markedly inhibited. This neuroimmune communication is termed the inflammatory reflex. The uncontrolled inflammation as a result from sepsis can lead to multiple organ failure, and even death. Experimental data show that regulation of the inflammatory reflex appears to be a useful interventional strategy for septic response. Herein, we review recent advances in the understanding of the inflammatory reflex and discuss potential therapeutics that vagal modulation of the immune system for the treatment of severe sepsis and septic shock.
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