Role of microglia autophagy and mitophagy in age-related neurodegenerative diseases DOI Creative Commons
Mingkai Lin, Hongwen Yu,

Qiuyan Xie

et al.

Frontiers in Aging Neuroscience, Journal Year: 2023, Volume and Issue: 14

Published: April 26, 2023

Microglia, characterized by responding to damage, regulating the secretion of soluble inflammatory mediators, and engulfing specific segments in central nervous system (CNS), function as key immune cells CNS. Emerging evidence suggests that microglia coordinate responses CNS play a pivotal role pathogenesis age-related neurodegenerative diseases (NDDs). Remarkably, autophagy participates regulation subcellular substances, which includes degradation misfolded proteins other harmful constituents produced neurons. Therefore, regulates neuronal homeostasis maintenance process neuroinflammation. In this review, we aimed at highlighting NDDs. Besides mechanistic co-interaction between different kinds NDDs, also emphasized potential therapeutic agents approaches could be utilized onset progression these through modulating autophagy, including promising nanomedicines. Our review provides valuable reference for subsequent studies focusing on treatments disorders. The exploration development nanomedicines greatly enhances current understanding

Language: Английский

HMGB1 mediates synaptic loss and cognitive impairment in an animal model of sepsis-associated encephalopathy DOI Creative Commons
Xiaoyu Yin,

Xiaohui Tang,

Shi-Xu Wang

et al.

Journal of Neuroinflammation, Journal Year: 2023, Volume and Issue: 20(1)

Published: March 11, 2023

Microglial activation-mediated neuroinflammation is one of the essential pathogenic mechanisms sepsis-associated encephalopathy (SAE). Mounting evidence suggests that high mobility group box-1 protein (HMGB1) plays a pivotal role in and SAE, yet mechanism by which HMGB1 induces cognitive impairment SAE remains unclear. Therefore, this study aimed to investigate underlying SAE.An model was established cecal ligation puncture (CLP); animals sham underwent cecum exposure alone without perforation. Mice inflachromene (ICM) were continuously injected with ICM intraperitoneally at daily dose 10 mg/kg for 9 days starting 1 h before CLP operation. The open field, novel object recognition, Y maze tests performed on 14-18 after surgery assess locomotor activity function. secretion, state microglia, neuronal measured immunofluorescence. Golgi staining detect changes morphology dendritic spine density. In vitro electrophysiology long-term potentiation (LTP) CA1 hippocampus. vivo neural oscillation hippocampus.CLP-induced accompanied increased secretion microglial activation. phagocytic capacity microglia enhanced, resulting aberrant pruning excitatory synapses loss reduced activity, impaired LTP, decreased theta Inhibiting treatment reversed these changes.HMGB1 activation, synaptic pruning, neuron dysfunction an animal leading impairment. These results suggest might be target treatment.

Language: Английский

Citations

64

Fisetin ameliorates cognitive impairment by activating mitophagy and suppressing neuroinflammation in rats with sepsis‐associated encephalopathy DOI
Hongguang Ding, Ya Li, Shenglong Chen

et al.

CNS Neuroscience & Therapeutics, Journal Year: 2021, Volume and Issue: 28(2), P. 247 - 258

Published: Nov. 27, 2021

Fisetin, the effective ingredient of traditional Chinese medicine named Cotinus coggygria, is recommended to be active therapeutic in many disorders. However, its role sepsis-associated encephalopathy (SAE) remains unclarified.Cecal ligation and puncture (CLP) operation was performed establish a rat model SAE. Rats were grouped according surgery fisetin administration. Cognitive impairment assessed by Morris water maze test. Disruption blood-brain barrier (BBB) integrity detected Evan's blue staining. The mitophagy, reactive oxygen species (ROS) generation, NLRP3 inflammasome activation, pro-inflammatory cytokines levels measured through western blot double immunofluorescence labeling. A transmission electron microscope applied for observation mitochondrial autophagosomes.Rats CLP group presented increased expression IL-1R1, pNF-κB, TNF-α, iNOS microglial cells, indicating severe inflammation central nervous system (CNS). Nevertheless, there no increase BBB permeability. Meanwhile, activated cerebral microvascular endothelial cells (CMECs), with an elevation caspase-1 IL-1β secretion into CNS. In addition, we found significantly improved cognitive dysfunction rats Neuroprotective effects might associated inhibition neuroinflammation, represented decreased microglia. Furthermore, induced scavenged ROS, blocked activation CMECs, as evidenced reduced release CNS.Collectively, fisetin-blocked via promoting mitophagy CMECs may suppress CNS, reduce contribute amelioration impairment.

Language: Английский

Citations

84

Beneficial effects of natural flavonoids on neuroinflammation DOI Creative Commons
Yu Chen,

Fu Peng,

Ziwei Xing

et al.

Frontiers in Immunology, Journal Year: 2022, Volume and Issue: 13

Published: Oct. 24, 2022

Neuroinflammation is the fundamental immune response against multiple factors in central nervous system and characterized by production of inflammatory mediators, activated microglia astrocytes, recruitment innate adaptive cells to sites, that contributes pathological process related brain diseases, such as Alzheimer’s disease, Parkinson’s depression, stroke. Flavonoids, a species important natural compounds, have been widely revealed alleviate neuroinflammation inhibiting pro-inflammatory elevating secretion anti-inflammatory factors, modulating polarization astrocyte, mainly via suppressing activation NLRP3 inflammasome, well NF-κB, MAPK, JAK/STAT pathways, promoting Nrf2, AMPK, BDNF/CREB, Wnt/β-Catenin, PI3k/Akt signals SIRT1-mediated HMGB1 deacetylation. This review will provide latest comprehensive knowledge on therapeutic benefits mechanisms flavonoids neuroinflammation, might be developed into food supplements or lead compounds for neuroinflammation-associated disorders.

Language: Английский

Citations

65

Endothelial dysfunction: Pathophysiology and therapeutic targets for sepsis-induced multiple organ dysfunction syndrome DOI Creative Commons
Fei Tang,

Xiaolan Zhao,

Li-Yue Xu

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 178, P. 117180 - 117180

Published: July 27, 2024

Sepsis and septic shock are critical medical conditions characterized by a systemic inflammatory response to infection, significantly contributing global mortality rates. The progression multiple organ dysfunction syndrome (MODS) represents the most severe complication of sepsis markedly increases clinical mortality. Central pathophysiology sepsis, endothelial cells play crucial role in regulating microcirculation maintaining barrier integrity across various organs tissues. Recent studies have underscored pivotal function development sepsis-induced MODS. This review aims provide comprehensive overview MODS, with specific focus on dysfunction. It also compiles compelling evidence regarding potential small molecules that could attenuate subsequent multi-organ damage modulating function. Thus, this serves as an essential resource for practitioners involved diagnosing, managing, providing intensive care associated injuries, emphasizing importance targeting enhance outcomes patients.

Language: Английский

Citations

15

Targeting novel regulated cell death:Ferroptosis, pyroptosis, and autophagy in sepsis-associated encephalopathy DOI Open Access

Jingjing Sun,

Joshua S. Fleishman, Xueyan Liu

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 174, P. 116453 - 116453

Published: March 20, 2024

Sepsis-associated encephalopathy (SAE), a common neurological complication of sepsis, is heterogenous complex clinical syndrome caused by the dysfunctional response host to infection. This leads excess mortality and morbidity worldwide. Despite relevance with high incidence, there lack understanding for its both acute/chronic pathogenesis therapeutic management. A better molecular mechanisms behind SAE may provide tools enhance efficacy. Mounting evidence indicates that some types non-apoptotic regulated cell death (RCD), such as ferroptosis, pyroptosis, autophagy, contribute SAE. Targeting these RCD meaningful targets future treatments against review summarizes core mechanism which We focus on emerging compounds can inhibit delineate their beneficial pharmacological effects Within this we suggest inhibition serve potential strategy

Language: Английский

Citations

14

Mechanism and role of mitophagy in the development of severe infection DOI Creative Commons

Lixiu Ma,

Tianyu Han,

Y M Zhan

et al.

Cell Death Discovery, Journal Year: 2024, Volume and Issue: 10(1)

Published: Feb. 19, 2024

Abstract Mitochondria produce adenosine triphosphate and potentially contribute to proinflammatory responses cell death. Mitophagy, as a conservative phenomenon, scavenges waste mitochondria their components in the cell. Recent studies suggest that severe infections develop alongside mitochondrial dysfunction mitophagy abnormalities. Restoring protects against excessive inflammation multiple organ failure sepsis. Here, we review normal process, its interaction with invading microorganisms immune system, summarize mechanism of during infection. We highlight critical role preventing

Language: Английский

Citations

13

Targeting selective autophagy and beyond: From underlying mechanisms to potential therapies DOI Creative Commons
Wei Ma, Yingying Lü, Xin Jin

et al.

Journal of Advanced Research, Journal Year: 2024, Volume and Issue: 65, P. 297 - 327

Published: May 14, 2024

Autophagy is an evolutionarily conserved turnover process for intracellular substances in eukaryotes, relying on lysosomal (in animals) or vacuolar yeast and plants) mechanisms. In the past two decades, emerging evidence suggests that, under specific conditions, autophagy can target particular macromolecules organelles degradation, a termed selective autophagy. Recently, accumulating studies have demonstrated that abnormality of closely associated with occurrence progression many human diseases, including neurodegenerative cancers, metabolic cardiovascular diseases. This review aims at systematically comprehensively introducing its role various while unravelling molecular mechanisms By providing theoretical basis development related small-molecule drugs as well treating this seeks to contribute understanding therapeutic potential. review, we introduce dissect major categories been discovered. We also focus recent advances underlying both classical non-classical Moreover, current situation targeting different types further summarized, valuable insights into discovery more candidate future. On other hand, reveal clinically relevant implementations are potentially autophagy, such predictive approaches treatments tailored individual patients.

Language: Английский

Citations

12

Mechanism of Salvia miltiorrhiza Bunge extract to alleviate Chronic Sleep Deprivation-Induced cognitive dysfunction in rats DOI Creative Commons
Chao Yin, Meiya Zhang, Shuna Jin

et al.

Phytomedicine, Journal Year: 2024, Volume and Issue: 130, P. 155725 - 155725

Published: May 12, 2024

Bidirectional communication between the gut microbiota and brain may play an essential role in cognitive dysfunction associated with chronic sleep deprivation(CSD). Salvia miltiorrhiza Bunge (Danshen, DS), a famous Chinese medicine functional tea, is extensively used to protect learning memory capacities, although mechanism of action remains unknown.

Language: Английский

Citations

11

Decreased excitatory and increased inhibitory transmission in the hippocampal CA1 drive neuroinflammation-induced cognitive impairments in mice DOI
Xin-miao Wu,

Cui-na Shi,

Kai Liu

et al.

Brain Behavior and Immunity, Journal Year: 2025, Volume and Issue: 128, P. 416 - 428

Published: April 24, 2025

Language: Английский

Citations

1

Mechanisms of Mitochondrial Malfunction in Alzheimer’s Disease: New Therapeutic Hope DOI Open Access
Showkat Ul Nabi, Andleeb Khan, Ehraz Mehmood Siddiqui

et al.

Oxidative Medicine and Cellular Longevity, Journal Year: 2022, Volume and Issue: 2022, P. 1 - 28

Published: May 14, 2022

Mitochondria play a critical role in neuron viability or death as it regulates energy metabolism and cell pathways. They are essential for cellular metabolism, reactive oxygen species production, apoptosis, Ca++ homeostasis, aging, regeneration. Mitophagy mitochondrial dynamics thus processes the quality control of mitochondria. Improvements several fundamental features biology susceptible neurons AD brains putative underlying mechanisms such changes have made significant progress. AD’s etiology has been reported by malfunction oxidative damage. According to recent articles, continual fusion fission balance mitochondria is vital their normal function maintenance. As result, shape inextricably linked. This study examines evidence suggesting that dysfunction plays early impact on pathology. Furthermore, roles discussed with link between autophagy also explored. In addition, research mitophagy this review. It goes into how these flaws affect control. advanced therapy techniques lifestyle adjustments lead improved management demonstrated, hence improving conditions contribute AD.

Language: Английский

Citations

34