1. Preoperative Chronic and Acute Pain Affects Postoperative Cognitive Function Mediated by Neurotransmitters.
- Author
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Ding X, Gao X, Wang Z, Jiang X, Lu S, Xu J, Qin G, Gu Z, and Huang D
- Subjects
- Acute Pain physiopathology, Animals, Chronic Pain physiopathology, Hepatectomy adverse effects, Hippocampus metabolism, Interleukin-1beta blood, Interleukin-6 blood, Male, Maze Learning, Mice, Mice, Inbred C57BL, Postoperative Cognitive Complications physiopathology, Prefrontal Cortex metabolism, Tumor Necrosis Factor-alpha blood, Acetylcholine metabolism, Acute Pain metabolism, Chronic Pain metabolism, Dopamine metabolism, Postoperative Cognitive Complications metabolism, Serotonin metabolism
- Abstract
The effective prevention of postoperative cognitive dysfunction (POCD) needs to be explored, and the effect of preoperative pain on POCD remains unclear. We established a chronic pain model induced by chronic constriction injury (CCI) and models of acute pain and anxiety without pain in mice that were subsequently subjected to partial hepatectomy surgery. Morris water maze (MWM) tests were performed to evaluate the learning and memory abilities of the mice. ELISA was used to measure IL-1β, IL-6, and TNF-α in serum, and HPLC-MS was used to detect neurotransmitters in the prefrontal cortices and hippocampi of the mice. The results indicated that chronic pain induced by CCI might have significantly impaired the learning and memory abilities of mice, while acute pain and anxiety without pain only affected the memory abilities of mice. Perioperative acute pain increased the level of IL-1β in serum, and CCI might have increased the level of IL-6. CCI and acute pain increased dopamine (DA) levels in the cortex, similar to anxiety. Like anxiety, CCI increased 5-hydroxytryptamine (5-HT) levels in the prefrontal cortex and hippocampus. Acute pain led to a decrease in the acetylcholine (ACH) level in the hippocampus. Our results suggest that acute pain and CCI-induced chronic pain might aggravate postoperative cognitive dysfunction via neurotransmitters and by changing the levels of inflammatory factors such as IL-1β and IL-6.
- Published
- 2021
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