4.8 Article

Optogenetic stimulation of the brainstem dorsal motor nucleus ameliorates acute pancreatitis

Journal

FRONTIERS IN IMMUNOLOGY
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2023.1166212

Keywords

acute pancreatitis; dorsal motor nucleus; vagus nerve; inflammation; cytokines; cholinergic anti-inflammatory pathway (CAP)

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Inflammation is a self-amplifying process that can result in tissue damage. The nervous system has evolved to detect inflammatory signals and respond with anti-inflammatory processes, including the cholinergic anti-inflammatory pathway mediated by the vagus nerve. This study used optogenetics to selectively activate vagus nerve fibers originating in the brainstem and found that stimulation of cholinergic neurons in the dorsal motor nucleus of the vagus significantly reduced the severity of pancreatitis.
IntroductionInflammation is an inherently self-amplifying process, resulting in progressive tissue damage when unresolved. A brake on this positive feedback system is provided by the nervous system which has evolved to detect inflammatory signals and respond by activating anti-inflammatory processes, including the cholinergic anti-inflammatory pathway mediated by the vagus nerve. Acute pancreatitis, a common and serious condition without effective therapy, develops when acinar cell injury activates intrapancreatic inflammation. Prior study has shown that electrical stimulation of the carotid sheath, which contains the vagus nerve, boosts the endogenous anti-inflammatory response and ameliorates acute pancreatitis, but it remains unknown whether these anti-inflammatory signals originate in the brain. MethodsHere, we used optogenetics to selectively activate efferent vagus nerve fibers originating in the brainstem dorsal motor nucleus of the vagus (DMN) and evaluated the effects on caerulein-induced pancreatitis. ResultsStimulation of the cholinergic neurons in the DMN significantly attenuates the severity of pancreatitis as indicated by reduced serum amylase, pancreatic cytokines, tissue damage, and edema. Either vagotomy or silencing cholinergic nicotinic receptor signaling by pre-administration of the antagonist mecamylamine abolishes the beneficial effects. DiscussionThese results provide the first evidence that efferent vagus cholinergic neurons residing in the brainstem DMN can inhibit pancreatic inflammation and implicate the cholinergic anti-inflammatory pathway as a potential therapeutic target for acute pancreatitis.

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