[HTML][HTML] Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function

AG Spiteri, CL Wishart, R Pamphlett, G Locatelli… - Acta …, 2022 - Springer
In neurological diseases, the actions of microglia, the resident myeloid cells of the CNS
parenchyma, may diverge from, or intersect with, those of recruited monocytes to drive …

[PDF][PDF] Damage-associated molecular patterns in inflammatory diseases

JS Roh, DH Sohn - Immune network, 2018 - synapse.koreamed.org
Damage-associated molecular patterns (DAMPs) are endogenous danger molecules that
are released from damaged or dying cells and activate the innate immune system by …

[HTML][HTML] Blood-brain barrier disruption by lipopolysaccharide and sepsis-associated encephalopathy

X Peng, Z Luo, S He, L Zhang, Y Li - Frontiers in cellular and infection …, 2021 - frontiersin.org
As a complex multicellular structure of the vascular system at the central nervous system
(CNS), the blood-brain barrier (BBB) separates the CNS from the system circulation and …

The integration of inflammaging in age-related diseases

T Fulop, JM Witkowski, F Olivieri, A Larbi - Seminars in immunology, 2018 - Elsevier
Aging is characterized by a morpho-functional adaptation, variably affecting major
physiological systems, depending on a complex interaction between genetic, environmental …

Dexmedetomidine attenuates sepsis-associated inflammation and encephalopathy via central α2A adrenoceptor

B Mei, J Li, Z Zuo - Brain, Behavior, and Immunity, 2021 - Elsevier
Sepsis-associated encephalopathy (SAE) is a significant clinical issue that is associated
with increased mortality and cost of health care. Dexmedetomidine, an α2 adrenoceptor …

[HTML][HTML] HMGB1: a common biomarker and potential target for TBI, neuroinflammation, epilepsy, and cognitive dysfunction

YN Paudel, MF Shaikh, A Chakraborti… - Frontiers in …, 2018 - frontiersin.org
High mobility group box protein 1 (HMGB1) is a ubiquitous nuclear protein released by glia
and neurons upon inflammasome activation and activates receptor for advanced glycation …

[HTML][HTML] Impact of HMGB1, RAGE, and TLR4 in Alzheimer's disease (AD): from risk factors to therapeutic targeting

YN Paudel, E Angelopoulou, C Piperi, I Othman… - Cells, 2020 - mdpi.com
Alzheimer's disease (AD) is a devastating neurodegenerative disorder and a leading cause
of dementia, with accumulation of amyloid-beta (Aβ) and neurofibrillary tangles (NFTs) as …

[HTML][HTML] Can an infection hypothesis explain the beta amyloid hypothesis of Alzheimer's disease?

T Fulop, JM Witkowski, K Bourgade, A Khalil… - Frontiers in aging …, 2018 - frontiersin.org
Alzheimer's disease (AD) is the most frequent type of dementia. The pathological hallmarks
of the disease are extracellular senile plaques composed of beta-amyloid peptide (Aβ) and …

The gut microbiome and Alzheimer's disease: Complex and bidirectional interactions

R Tarawneh, E Penhos - Neuroscience & Biobehavioral Reviews, 2022 - Elsevier
Structural and functional alterations to the gut microbiome, referred to as gut dysbiosis, have
emerged as potential key mediators of neurodegeneration and Alzheimer disease (AD) …

[HTML][HTML] High mobility group box-1 and blood–brain barrier disruption

M Nishibori, D Wang, D Ousaka, H Wake - Cells, 2020 - mdpi.com
Increasing evidence suggests that inflammatory responses are involved in the progression
of brain injuries induced by a diverse range of insults, including ischemia, hemorrhage …