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bioRxiv · 10.1101/2023.10.10.561630

The Role of PKR on Modulating Neuroinflammation and Cognitive Dysfunctions in a Peripheral Inflammation Model

Cheng, W.-Y.·Lee, X.-Z.·Lai, M. S.-L.·Ho, Y.-S.·Chang, R. C.-C.
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Abstract

Systemic inflammation may promote neuroinflammation and neurodegeneration. The double-stranded RNA-dependent protein kinase (PKR) is a key signaling molecule that regulates immune responses. This study aims to examine the role of PKR in regulating systemic inflammation-induced neuroinflammation and cognitive dysfunctions using a laparotomy mouse model. In the first part, wild-type C57BL/6J and C57BL/6-Tg(CD68-EGFP)1Drg/J mice were assigned to undergo either laparotomy with sevoflurane anesthesia or sevoflurane alone to examine effects of systemic inflammation on neuroinflammation and cognition. In the second part, PKR-/- mice were used to study the role of PKR in modulating laparotomy-induced systemic inflammation, neuroinflammation, and cognition. For the third part, PKR was inhibited selectively in cholinergic neurons of ChAT-IRES-Cre-eGFP mice via intracerebroventricular injection of rAAV-DIO-PKR-K296R. This examined the effects of inhibiting PKR in cholinergic neurons on glucose metabolism and cognition in the laparotomy model. Our study revealed that genetic deletion of PKR in mice potently attenuated the laparotomy-induced peripheral and neural inflammation and cognitive deficits. Furthermore, inhibiting PKR in the cholinergic neurons rescued the laparotomy-induced brain glucose hypometabolism and cognitive impairment. Our results demonstrated the critical role of PKR in regulating neuroinflammation and cognitive dysfunctions in a peripheral inflammation model. PKR could be a pharmacological target for treating systemic inflammation-induced neuroinflammation and cognitive dysfunctions.

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Cheng, W.-Y., Lee, X.-Z., Lai, M. S.-L., Ho, Y.-S., Chang, R. C.-C.. 2023-10-10. The Role of PKR on Modulating Neuroinflammation and Cognitive Dysfunctions in a Peripheral Inflammation Model. https://doi.org/10.1101/2023.10.10.561630

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