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Sphingosine kinase 1 knockout alleviates hepatic ischemia/reperfusion injury by attenuating inflammation and oxidative stress in mice.
Hepatobiliary Pancreat Dis Int. 2019 Jun; 18(3):255-265.HP

Abstract

BACKGROUND

Hepatic ischemia/reperfusion (I/R) injury remains a significant problem in clinical practice. Sphingosine kinase 1 (SphK1) phosphorylates sphingosine to sphingosine-1-phosphate (S1P) which participates in multiple bioactive processes. However, little is known about the role of SphK1 in hepatic I/R injury. This study aimed to investigate the effect of SphK1 knockout on liver I/R injury and to explore underlying mechanisms.

METHODS

SphK1 knockout and wild type mice were subjected to 70% partial hepatic I/R. Serum alanine aminotransferase was determined to indicate the degree of liver damage. Hematoxylin-eosin staining and TUNEL assay were used to assess histological changes and hepatocellular apoptosis, respectively. Immunohistochemistry was performed to detect the expression and translocation of phosphorylated p65 and signal transducer and activator of transcription 3 (STAT3). Western blotting was used to determine the expression of S1P receptor 1 (S1PR1), phosphorylated p65 and STAT3. Real-time PCR was used to demonstrate the changes of proinflammatory cytokines. Oxidative stress markers were also determined through biochemical assays.

RESULTS

SphK1 knockout significantly ameliorated I/R-induced liver damage, mitigated liver tissue necrosis and apoptosis compared with wild type control. I/R associated inflammation was alleviated in SphK1 knockout mice as demonstrated by attenuated expression of S1PR1 and reduced phosphorylation of nuclear factor kappa B p65 and STAT3. The proinflammatory cytokines interleukin-1β, interleukin-6 and tumor necrosis factor-α were also inhibited by SphK1 genetic deletion. The oxidative stress markers were lower in SphK1 knockout mice after I/R injury than wild type mice.

CONCLUSIONS

Knockout of SphK1 significantly alleviated damage after hepatic I/R injury, possibly through inhibiting inflammation and oxidative stress. SphK1 may be a novel and potent target in clinical practice in I/R-related liver injury.

Authors+Show Affiliations

Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China; Department of Hepatobiliary Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.Department of Hepatobiliary Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China; Department of Hepatobiliary Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China; Department of Hepatobiliary Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.Department of Gastroenterology, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China.Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital, Drum Tower Clinical College of Nanjing Medical University, Nanjing 210008, China; Department of Hepatobiliary Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China. Electronic address: chunpingjiang@163.com.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

31027910

Citation

Qiang, Guang-Hui, et al. "Sphingosine Kinase 1 Knockout Alleviates Hepatic Ischemia/reperfusion Injury By Attenuating Inflammation and Oxidative Stress in Mice." Hepatobiliary & Pancreatic Diseases International : HBPD INT, vol. 18, no. 3, 2019, pp. 255-265.
Qiang GH, Wang ZX, Ji AL, et al. Sphingosine kinase 1 knockout alleviates hepatic ischemia/reperfusion injury by attenuating inflammation and oxidative stress in mice. Hepatobiliary Pancreat Dis Int. 2019;18(3):255-265.
Qiang, G. H., Wang, Z. X., Ji, A. L., Wu, J. Y., Cao, Y., Zhang, G., Zhang, Y. Y., & Jiang, C. P. (2019). Sphingosine kinase 1 knockout alleviates hepatic ischemia/reperfusion injury by attenuating inflammation and oxidative stress in mice. Hepatobiliary & Pancreatic Diseases International : HBPD INT, 18(3), 255-265. https://doi.org/10.1016/j.hbpd.2019.04.001
Qiang GH, et al. Sphingosine Kinase 1 Knockout Alleviates Hepatic Ischemia/reperfusion Injury By Attenuating Inflammation and Oxidative Stress in Mice. Hepatobiliary Pancreat Dis Int. 2019;18(3):255-265. PubMed PMID: 31027910.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Sphingosine kinase 1 knockout alleviates hepatic ischemia/reperfusion injury by attenuating inflammation and oxidative stress in mice. AU - Qiang,Guang-Hui, AU - Wang,Zhong-Xia, AU - Ji,An-Lai, AU - Wu,Jun-Yi, AU - Cao,Yin, AU - Zhang,Guang, AU - Zhang,Yi-Yang, AU - Jiang,Chun-Ping, Y1 - 2019/04/05/ PY - 2018/10/26/received PY - 2019/04/01/accepted PY - 2019/4/28/pubmed PY - 2020/1/22/medline PY - 2019/4/28/entrez KW - Inflammation KW - Ischemia/reperfusion injury KW - Oxidative stress KW - Sphingosine kinase 1 SP - 255 EP - 265 JF - Hepatobiliary & pancreatic diseases international : HBPD INT JO - Hepatobiliary Pancreat Dis Int VL - 18 IS - 3 N2 - BACKGROUND: Hepatic ischemia/reperfusion (I/R) injury remains a significant problem in clinical practice. Sphingosine kinase 1 (SphK1) phosphorylates sphingosine to sphingosine-1-phosphate (S1P) which participates in multiple bioactive processes. However, little is known about the role of SphK1 in hepatic I/R injury. This study aimed to investigate the effect of SphK1 knockout on liver I/R injury and to explore underlying mechanisms. METHODS: SphK1 knockout and wild type mice were subjected to 70% partial hepatic I/R. Serum alanine aminotransferase was determined to indicate the degree of liver damage. Hematoxylin-eosin staining and TUNEL assay were used to assess histological changes and hepatocellular apoptosis, respectively. Immunohistochemistry was performed to detect the expression and translocation of phosphorylated p65 and signal transducer and activator of transcription 3 (STAT3). Western blotting was used to determine the expression of S1P receptor 1 (S1PR1), phosphorylated p65 and STAT3. Real-time PCR was used to demonstrate the changes of proinflammatory cytokines. Oxidative stress markers were also determined through biochemical assays. RESULTS: SphK1 knockout significantly ameliorated I/R-induced liver damage, mitigated liver tissue necrosis and apoptosis compared with wild type control. I/R associated inflammation was alleviated in SphK1 knockout mice as demonstrated by attenuated expression of S1PR1 and reduced phosphorylation of nuclear factor kappa B p65 and STAT3. The proinflammatory cytokines interleukin-1β, interleukin-6 and tumor necrosis factor-α were also inhibited by SphK1 genetic deletion. The oxidative stress markers were lower in SphK1 knockout mice after I/R injury than wild type mice. CONCLUSIONS: Knockout of SphK1 significantly alleviated damage after hepatic I/R injury, possibly through inhibiting inflammation and oxidative stress. SphK1 may be a novel and potent target in clinical practice in I/R-related liver injury. SN - 1499-3872 UR - https://www.unboundmedicine.com/medline/citation/31027910/Sphingosine_kinase_1_knockout_alleviates_hepatic_ischemia/reperfusion_injury_by_attenuating_inflammation_and_oxidative_stress_in_mice_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S1499-3872(19)30067-0 DB - PRIME DP - Unbound Medicine ER -