دورية أكاديمية

Salidroside ameliorates acute liver transplantation rejection in rats by inhibiting neutrophil extracellular trap formation.

التفاصيل البيبلوغرافية
العنوان: Salidroside ameliorates acute liver transplantation rejection in rats by inhibiting neutrophil extracellular trap formation.
المؤلفون: Qin X; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China.; Department of General Surgery and Trauma Surgery, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Structural Birth Defect and Reconstruction, Chongqing 400014, China., Wang H; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Li Q; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Hu D; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Wang L; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Zhou B; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Liao R; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China., Liu Y; Department of Hepatobiliary Surgery, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400042, China.
المصدر: Acta biochimica et biophysica Sinica [Acta Biochim Biophys Sin (Shanghai)] 2024 Jun 25; Vol. 56 (6), pp. 833-843.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: China Science Publishing & Media Ltd Country of Publication: China NLM ID: 101206716 Publication Model: Print Cited Medium: Internet ISSN: 1745-7270 (Electronic) Linking ISSN: 16729145 NLM ISO Abbreviation: Acta Biochim Biophys Sin (Shanghai) Subsets: MEDLINE
أسماء مطبوعة: Publication: 2022- : Shanghai : China Science Publishing & Media Ltd.
Original Publication: Shanghai : Shanghai Scientific and Technical Publishers, 2004-
مواضيع طبية MeSH: Phenols*/pharmacology , Glucosides*/pharmacology , Liver Transplantation* , Extracellular Traps*/drug effects , Extracellular Traps*/metabolism , Graft Rejection*/prevention & control , Graft Rejection*/pathology , Graft Rejection*/drug therapy , Graft Rejection*/metabolism , HMGB1 Protein*/metabolism , Toll-Like Receptor 4*/metabolism , Neutrophils*/drug effects , Neutrophils*/metabolism, Animals ; Male ; Rats ; Rats, Sprague-Dawley ; Liver/drug effects ; Liver/pathology ; Liver/metabolism ; MAP Kinase Signaling System/drug effects ; Apoptosis/drug effects
مستخلص: Acute rejection is an important factor affecting the survival of recipients after liver transplantation. Salidroside has various properties, including anti-inflammatory, antioxidant, and hepatoprotective properties. This study aims to investigate whether salidroside can prevent acute rejection after liver transplantation and to examine the underlying mechanisms involved. An in vivo acute rejection model is established in rats that are pretreated with tacrolimus (1 mg/kg/d) or salidroside (10 or 20 mg/kg/d) for seven days after liver transplantation. In addition, an in vitro experiment is performed using neutrophils incubated with salidroside (1, 10, 50 or 100 μM). Hematoxylin-eosin staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, immunosorbent assays, immunofluorescence analysis, Evans blue staining, and western blot analysis are performed to examine the impact of salidroside on NET formation and acute rejection in vitro and in vivo . We find that Salidroside treatment reduces pathological liver damage, serum aminotransferase level, and serum levels of IL-1β, IL-6, and TNF-α in vivo . The expressions of proteins associated with the HMGB1/TLR-4/MAPK signaling pathway (HMGB1, TLR-4, p-ERK1/2, p-JNK, p-P38, cleaved caspase-3, cleaved caspase-9, Bcl-2, Bax, IL-1β, TNF-α, and IL-6) are also decreased after salidroside treatment. In vitro experiments show that the release of HMGB1/TLR-4/MAPK signaling pathway-associated proteins from neutrophils treated with lipopolysaccharide is decreased by salidroside. Moreover, salidroside inhibits NETosis and protects against acute rejection by regulating the HMGB1/TLR-4/MAPK signaling pathway. Furthermore, salidroside combined with tacrolimus has a better effect than either of the other treatments alone. In summary, salidroside can prevent acute liver rejection after liver transplantation by reducing neutrophil extracellular trap development through the HMGB1/TLR-4/MAPK signaling pathway.
References: Hepatobiliary Pancreat Dis Int. 2019 Dec;18(6):517-524. (PMID: 31151807)
Cells. 2023 Apr 04;12(7):. (PMID: 37048161)
Front Pharmacol. 2019 Dec 13;10:1433. (PMID: 31920641)
Evid Based Complement Alternat Med. 2020 Sep 26;2020:9568647. (PMID: 33062029)
Acta Neuropathol Commun. 2019 Jun 10;7(1):94. (PMID: 31177989)
Front Immunol. 2021 Jun 10;12:679398. (PMID: 34177922)
Transplantation. 2022 Feb 1;106(2):e126-e140. (PMID: 34534191)
Front Pharmacol. 2020 Sep 08;11:544124. (PMID: 33013386)
Eur J Pharmacol. 2017 Jul 5;806:32-42. (PMID: 28411054)
PLoS One. 2015 Jun 12;10(6):e0129788. (PMID: 26070151)
Hepatology. 2015 Aug;62(2):600-14. (PMID: 25855125)
Transpl Immunol. 2021 Oct;68:101434. (PMID: 34216758)
Clin Immunol. 2020 Jul;216:108461. (PMID: 32437924)
J Cell Physiol. 2019 Sep;234(9):16367-16375. (PMID: 30805938)
Phytother Res. 2018 Nov;32(11):2247-2255. (PMID: 30047580)
Blood. 2012 Oct 11;120(15):3118-25. (PMID: 22919032)
J Hepatol. 2015 Apr;62(1 Suppl):S170-85. (PMID: 25920086)
Front Cell Infect Microbiol. 2022 Aug 12;12:927193. (PMID: 36034701)
Toxicology. 2021 Sep;461:152905. (PMID: 34450210)
Biochem Biophys Res Commun. 2021 Jan 1;534:408-414. (PMID: 33256982)
J Leukoc Biol. 2021 Nov;110(5):987-998. (PMID: 33784425)
Hepatobiliary Pancreat Dis Int. 2023 Feb;22(1):14-21. (PMID: 36328894)
J Hepatol. 2019 Feb;70(2):328-334. (PMID: 30658734)
Blood. 2016 Nov 17;128(20):2435-2449. (PMID: 27574188)
Chem Biol Interact. 2021 Apr 25;339:109268. (PMID: 33617801)
Nat Rev Immunol. 2018 Feb;18(2):134-147. (PMID: 28990587)
Am J Physiol Cell Physiol. 2013 Aug 1;305(3):C348-54. (PMID: 23720022)
Hepatology. 2021 Dec;74(6):3056-3073. (PMID: 34292604)
Biomed Pharmacother. 2022 Dec;156:113746. (PMID: 36228376)
Hepatology. 2021 Mar;73(3):1158-1175. (PMID: 32426849)
Clin Gastroenterol Hepatol. 2017 Apr;15(4):584-593.e2. (PMID: 27567694)
Hum Pathol. 2022 Sep;127:67-77. (PMID: 35728694)
J Vis Exp. 2018 Mar 19;(133):. (PMID: 29608158)
Drug Des Devel Ther. 2017 Jul 03;11:1989-2006. (PMID: 28721018)
Br J Pharmacol. 2019 Sep;176(17):3350-3363. (PMID: 31206609)
Clin Gastroenterol Hepatol. 2023 Jul;21(8):2150-2166. (PMID: 37084928)
Mol Med Rep. 2018 Oct;18(4):3760-3768. (PMID: 30132527)
Exp Cell Res. 2021 Sep 1;406(1):112719. (PMID: 34273405)
فهرسة مساهمة: Keywords: HMGB1; acute rejection; liver transplantation; neutrophil extracellular traps; salidroside
المشرفين على المادة: M983H6N1S9 (rhodioloside)
0 (Phenols)
0 (Glucosides)
0 (HMGB1 Protein)
0 (Toll-Like Receptor 4)
0 (Tlr4 protein, rat)
0 (Hbp1 protein, rat)
تواريخ الأحداث: Date Created: 20240508 Date Completed: 20240613 Latest Revision: 20240703
رمز التحديث: 20240703
مُعرف محوري في PubMed: PMC11214976
DOI: 10.3724/abbs.2024055
PMID: 38716542
قاعدة البيانات: MEDLINE
الوصف
تدمد:1745-7270
DOI:10.3724/abbs.2024055