2022
DOI: 10.1016/j.jchemneu.2022.102138
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Ghrelin inhibits early brain injury due to subarachnoid hemorrhage via the Tim-3-mediated HMGB1/NF-κB pathway

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Cited by 2 publications
(1 citation statement)
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“…DAMPs, an innate immune response to molecules released from the extracellular and intracellular space of damaged tissue or dead cells, are essential in response to inflammation progression [ 66 ]. Notably, the high-mobility group protein B1 (HMGB1), a typical DAMP, plays an integral role in the regulation of neuroinflammation following a SAH [ 67 , 68 ]. After a SAH, HMGB1, released from necrotic neurons, could induce cytokine release and leukocyte recruitment and then trigger the inflammatory response after interaction with TLR4 and the receptor for advanced glycation end products (RAGEs) [ 69 ].…”
Section: The Therapeutic Role Of Sirt1 In Sahsmentioning
confidence: 99%
“…DAMPs, an innate immune response to molecules released from the extracellular and intracellular space of damaged tissue or dead cells, are essential in response to inflammation progression [ 66 ]. Notably, the high-mobility group protein B1 (HMGB1), a typical DAMP, plays an integral role in the regulation of neuroinflammation following a SAH [ 67 , 68 ]. After a SAH, HMGB1, released from necrotic neurons, could induce cytokine release and leukocyte recruitment and then trigger the inflammatory response after interaction with TLR4 and the receptor for advanced glycation end products (RAGEs) [ 69 ].…”
Section: The Therapeutic Role Of Sirt1 In Sahsmentioning
confidence: 99%