S1PR3 agonism and S1P lyase inhibition rescue mice in the severe state of experimental sepsis-Reference-Cited by-同舟云学术

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S1PR3 agonism and S1P lyase inhibition rescue mice in the severe state of experimental sepsis

Published:2024-05 Issue: Volume:174 Page:116575
ISSN:0753-3322
Container-title:Biomedicine & Pharmacotherapy
language:en
Short-container-title:Biomedicine & Pharmacotherapy

Author:

Ziegler Anke C.,Haider Raphael S.,Hoffmann Carsten,Gräler Markus H.

Funder

DFG

Bundesministerium für Bildung und Forschung Dienststelle Berlin

Publisher

Elsevier BV

Reference63 articles.

1. The third international consensus definitions for sepsis and septic shock (Sepsis-3);Singer;JAMA,2016

2. Global, regional, and national sepsis incidence and mortality, 1990-2017: analysis for the Global Burden of Disease Study;Rudd;Lancet,2020

3. The immunopathogenesis of sepsis;Cohen;Nature,2002

4. Host innate immune responses to sepsis;Wiersinga;Virulence,2014

5. The immunopathology of sepsis and potential therapeutic targets;van der Poll;Nat. Rev. Immunol.,2017

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1. Hydroxysafflor yellow A, a natural food pigment, ameliorates atherosclerosis in ApoE^−/− mice by inhibiting the SphK1/S1P/S1PR3 pathway;Food Science & Nutrition;2024-09-14

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3. Research progress of sphingosine 1-phosphate receptor 3 in the cardiovascular system;Perioperative Precision Medicine;2024-06-30

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