» Articles » PMID: 30180861

Complement Activation Contributes to Perioperative Neurocognitive Disorders in Mice

Overview
Publisher Biomed Central
Date 2018 Sep 6
PMID 30180861
Citations 34
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The complement system plays an important role in many neurological disorders. Complement modulation, including C3/C3a receptor signaling, shows promising therapeutic effects on cognition and neurodegeneration. Yet, the implications for this pathway in perioperative neurocognitive disorders (PND) are not well established. Here, we evaluated the possible role for C3/C3a receptor signaling after orthopedic surgery using an established mouse model of PND.

Methods: A stabilized tibial fracture surgery was performed in adult male C57BL/6 mice under general anesthesia and analgesia to induce PND-like behavior. Complement activation was assessed in the hippocampus and choroid plexus. Changes in hippocampal neuroinflammation, synapse numbers, choroidal blood-cerebrospinal fluid barrier (BCSFB) integrity, and hippocampal-dependent memory function were evaluated after surgery and treatment with a C3a receptor blocker.

Results: C3 levels and C3a receptor expression were specifically increased in hippocampal astrocytes and microglia after surgery. Surgery-induced neuroinflammation and synapse loss in the hippocampus were attenuated by C3a receptor blockade. Choroidal BCSFB dysfunction occurred 1 day after surgery and was attenuated by C3a receptor blockade. Administration of exogenous C3a exacerbated cognitive decline after surgery, whereas C3a receptor blockade improved hippocampal-dependent memory function.

Conclusions: Orthopedic surgery activates complement signaling. C3a receptor blockade may be therapeutically beneficial to attenuate neuroinflammation and PND.

Citing Articles

Identification of Key Genes in Esketamine's Therapeutic Effects on Perioperative Neurocognitive Disorders via Transcriptome Sequencing.

Hu W, Luo J, Li H, Luo Y, Zhang X, Wu Z Drug Des Devel Ther. 2025; 19:981-1000.

PMID: 39974608 PMC: 11836629. DOI: 10.2147/DDDT.S510752.


Recent Advances in the Mechanisms of Postoperative Neurocognitive Dysfunction: A Narrative Review.

Wang T, Huang X, Sun S, Wang Y, Han L, Zhang T Biomedicines. 2025; 13(1).

PMID: 39857699 PMC: 11762480. DOI: 10.3390/biomedicines13010115.


Microglia mediate memory dysfunction via excitatory synaptic elimination in a fracture surgery mouse model.

Li S, Liu H, Lv P, Yao Y, Peng L, Xia T J Neuroinflammation. 2024; 21(1):227.

PMID: 39285282 PMC: 11406843. DOI: 10.1186/s12974-024-03216-2.


The schizophrenia risk gene C4 induces pathological synaptic loss by impairing AMPAR trafficking.

Phadke R, Brack A, Fournier L, Kruzich E, Sha M, Picard I Mol Psychiatry. 2024; 30(2):796-809.

PMID: 39227431 PMC: 11746135. DOI: 10.1038/s41380-024-02701-7.


Foxq1 activates CB2R with oleamide to alleviate POCD.

Wu X, Wu Y, Tang F, Wang Y, Li C, Wu S Brain Pathol. 2024; 35(1):e13289.

PMID: 39046224 PMC: 11669408. DOI: 10.1111/bpa.13289.


References
1.
Steffen B, Breier G, Butcher E, Schulz M, Engelhardt B . ICAM-1, VCAM-1, and MAdCAM-1 are expressed on choroid plexus epithelium but not endothelium and mediate binding of lymphocytes in vitro. Am J Pathol. 1996; 148(6):1819-38. PMC: 1861637. View

2.
Silbert B, Evered L, Scott D, McMahon S, Choong P, Ames D . Preexisting cognitive impairment is associated with postoperative cognitive dysfunction after hip joint replacement surgery. Anesthesiology. 2015; 122(6):1224-34. DOI: 10.1097/ALN.0000000000000671. View

3.
Bialas A, Presumey J, Das A, van der Poel C, Lapchak P, Mesin L . Microglia-dependent synapse loss in type I interferon-mediated lupus. Nature. 2017; 546(7659):539-543. DOI: 10.1038/nature22821. View

4.
Terrando N, Gomez-Galan M, Yang T, Carlstrom M, Gustavsson D, Harding R . Aspirin-triggered resolvin D1 prevents surgery-induced cognitive decline. FASEB J. 2013; 27(9):3564-71. DOI: 10.1096/fj.13-230276. View

5.
Griffin R, Costigan M, Brenner G, Ma C, Scholz J, Moss A . Complement induction in spinal cord microglia results in anaphylatoxin C5a-mediated pain hypersensitivity. J Neurosci. 2007; 27(32):8699-708. PMC: 6672952. DOI: 10.1523/JNEUROSCI.2018-07.2007. View