Luteolin Ameliorates Testis Injury and Blood-Testis Barrier Disruption through the Nrf2 Signaling Pathway and by Upregulating Cx43.

SCOPE Luteolin, a natural flavonoid, displays protective activities to testicular tissue. However, the molecular mechanisms are still unclear. In this study, the aim is to identify the protective effects and underlying mechanisms of luteolin against triptolide (TP)-induced damage of testicular tissue. METHODS AND RESULTS Pre-incubation of Sertoli cells (SCs) with luteolin results in a significant reduction of TP-induced apoptotic cells, which occurs concomitantly with the effective inhibition of reactive oxygen species accumulation. Luteolin results in a significant reduction in testicular damage and spermatogenesis dysfunction in a mouse model of testicular damage. Mechanistic studies reveal that luteolin significantly triggers Nrf2 translocation, increases antioxidant response element-luciferase reporter activity, and induces antioxidant enzyme expression. Nrf2 siRNA reduces luteolin-induced protection in SCs. Besides inhibiting apoptosis, luteolin recovers the blood-testis barrier (BTB) integrity by upregulating connexin43 (Cx43) expression. Moreover, specifically blocked Cx43 activity completely blocks repairmen of luteolin to BTB values. In accordance with in vitro results, luteolin suppresses testicular injury and spermatogenesis dysfunction by activation of Nrf2 and Cx43 in a testicular injury model. CONCLUSION Luteolin is identified as a novel active ingredient that contributes to the protective activity in testicular damage through activating the Nrf2 signaling pathway and by upregulating Cx43.

[1]  A. Risvanli,et al.  Effect of gestational diabetes mellitus on testis and pancreatic tissues of male offspring , 2018, Andrologia.

[2]  M. Uysal,et al.  Effects of resveratrol on high-fructose-induced testis injury in rats , 2018, Ultrastructural pathology.

[3]  A. Chuturgoon,et al.  Naringenin attenuates highly active antiretroviral therapy‐induced sperm DNA fragmentations and testicular toxicity in Sprague‐Dawley rats , 2018, Andrology.

[4]  B. Ma,et al.  Triptolide induces Sertoli cell apoptosis in mice via ROS/JNK-dependent activation of the mitochondrial pathway and inhibition of Nrf2-mediated antioxidant response , 2017, Acta Pharmacologica Sinica.

[5]  M. Alves,et al.  Evaluation of the Purity of Sertoli Cell Primary Cultures. , 2018, Methods in molecular biology.

[6]  M. Alves,et al.  Establishment of Primary Culture of Sertoli Cells. , 2018, Methods in molecular biology.

[7]  P. Roumaud,et al.  Influences of flavones on cell viability and cAMP-dependent steroidogenic gene regulation in MA-10 Leydig cells , 2018, Cell Biology and Toxicology.

[8]  Shengshou Hu,et al.  Cardiomyopathy-Associated Gene 1-Sensitive PKC-Dependent Connexin 43 Expression and Phosphorylation in Left Ventricular Noncompaction Cardiomyopathy , 2017, Cellular Physiology and Biochemistry.

[9]  A. Lenzi,et al.  The environment and male reproduction: The effect of cadmium exposure on reproductive function and its implication in fertility. , 2017, Reproductive toxicology.

[10]  C. Cheng,et al.  Perfluorooctanesulfonate (PFOS)-induced Sertoli cell injury through a disruption of F-actin and microtubule organization is mediated by Akt1/2 , 2017, Scientific Reports.

[11]  Chun-lan Long,et al.  Urban fine particulate matter exposure causes male reproductive injury through destroying blood-testis barrier (BTB) integrity. , 2017, Toxicology letters.

[12]  Zhiquan Chen,et al.  Connexin43 regulates high glucose‐induced expression of fibronectin, ICAM‐1 and TGF‐&bgr;1 via Nrf2/ARE pathway in glomerular mesangial cells , 2017, Free radical biology & medicine.

[13]  Jingjing Lu,et al.  Regulation of Sirt1/Nrf2/TNF-α signaling pathway by luteolin is critical to attenuate acute mercuric chloride exposure induced hepatotoxicity , 2016, Scientific Reports.

[14]  P. Stanton Regulation of the blood-testis barrier. , 2016, Seminars in cell & developmental biology.

[15]  Yanqin Yang,et al.  Activation of SIRT3 attenuates triptolide-induced toxicity through closing mitochondrial permeability transition pore in cardiomyocytes. , 2016, Toxicology in vitro : an international journal published in association with BIBRA.

[16]  Shih-Yin Chen,et al.  Luteolin inhibits viral-induced inflammatory response in RAW264.7 cells via suppression of STAT1/3 dependent NF-κB and activation of HO-1. , 2016, Free radical biology & medicine.

[17]  L. Senggunprai,et al.  Luteolin induces cholangiocarcinoma cell apoptosis through the mitochondrial‐dependent pathway mediated by reactive oxygen species , 2016, The Journal of pharmacy and pharmacology.

[18]  B. Silvestrini,et al.  Connexin 43 reboots meiosis and reseals blood‐testis barrier following toxicant‐mediated aspermatogenesis and barrier disruption , 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[19]  D. Cyr,et al.  Roles of connexins in testis development and spermatogenesis. , 2016, Seminars in cell & developmental biology.

[20]  Hong Tang,et al.  Luteolin Inhibits Hepatitis B Virus Replication through Extracellular Signal-Regulated Kinase-Mediated Down-Regulation of Hepatocyte Nuclear Factor 4α Expression. , 2016, Molecular pharmaceutics.

[21]  Fei Li,et al.  PRPS2 Expression Correlates with Sertoli-Cell Only Syndrome and Inhibits the Apoptosis of TM4 Sertoli Cells. , 2015, The Journal of urology.

[22]  Fang Zhao,et al.  Protection of Quercetin against Triptolide-induced apoptosis by suppressing oxidative stress in rat Leydig cells. , 2015, Chemico-biological interactions.

[23]  Qi Zhang,et al.  Triptolide disrupts fatty acids and peroxisome proliferator-activated receptor (PPAR) levels in male mice testes followed by testicular injury: A GC-MS based metabolomics study. , 2015, Toxicology.

[24]  Yanqin Yang,et al.  Autophagy plays an important role in triptolide-induced apoptosis in cardiomyocytes. , 2015, Toxicology letters.

[25]  M. Aldemir,et al.  Evaluation of the protective effect of quercetin against cisplatin‐induced renal and testis tissue damage and sperm parameters in rats , 2014, Andrologia.

[26]  Liang Jinqiang,et al.  Triptolide-induced oxidative stress involved with Nrf2 contribute to cardiomyocyte apoptosis through mitochondrial dependent pathways. , 2014, Toxicology letters.

[27]  Jingying Zhu,et al.  Involvement of CaM-CaMKII-ERK in bisphenol A-induced Sertoli cell apoptosis. , 2014, Toxicology.

[28]  L. Luo,et al.  Luteolin is effective in the non‐small cell lung cancer model with L858R/T790M EGF receptor mutation and erlotinib resistance , 2014, British journal of pharmacology.

[29]  J. Dufour,et al.  Sertoli cells--immunological sentinels of spermatogenesis. , 2014, Seminars in cell & developmental biology.

[30]  Xinyu Lu,et al.  Luteolin provides neuroprotection in models of traumatic brain injury via the Nrf2-ARE pathway. , 2014, Free radical biology & medicine.

[31]  H. Liu,et al.  Involvement of activating ERK1/2 through G protein coupled receptor 30 and estrogen receptor α/β in low doses of bisphenol A promoting growth of Sertoli TM4 cells. , 2014, Toxicology letters.

[32]  R. Brehm,et al.  Loss of connexin43 (Cx43) in Sertoli cells leads to spatio-temporal alterations in occludin expression. , 2014, Histology and histopathology.

[33]  C. Cheng,et al.  Perfluorooctanesulfonate (PFOS) perturbs male rat Sertoli cell blood-testis barrier function by affecting F-actin organization via p-FAK-Tyr(407): an in vitro study. , 2014, Endocrinology.

[34]  Fei-Fei Gan,et al.  Antioxidant and Nrf2 inducing activities of luteolin, a flavonoid constituent in Ixeris sonchifolia Hance, provide neuroprotective effects against ischemia-induced cellular injury. , 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[35]  Xinru Wang,et al.  Sertoli cell is a potential target for perfluorooctane sulfonate-induced reproductive dysfunction in male mice. , 2013, Toxicological sciences : an official journal of the Society of Toxicology.

[36]  Huibi Xu,et al.  Acute and subacute toxicity studies on triptolide and triptolide-loaded polymeric micelles following intravenous administration in rodents. , 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[37]  J. Gilleron,et al.  Hexavalent chromium at low concentration alters Sertoli cell barrier and connexin 43 gap junction but not claudin-11 and N-cadherin in the rat seminiferous tubule culture model. , 2013, Toxicology and applied pharmacology.

[38]  R. Braun,et al.  Germ Cell Migration Across Sertoli Cell Tight Junctions , 2012, Science.

[39]  B. Ma,et al.  Strontium fructose 1,6-diphosphate prevents bone loss in a rat model of postmenopausal osteoporosis via the OPG/RANKL/RANK pathway , 2012, Acta Pharmacologica Sinica.

[40]  C. Cheng,et al.  Connexin 43 is critical to maintain the homeostasis of the blood–testis barrier via its effects on tight junction reassembly , 2010, Proceedings of the National Academy of Sciences.

[41]  J. Gilleron,et al.  Major involvement of connexin 43 in seminiferous epithelial junction dynamics and male fertility. , 2010, Developmental biology.

[42]  Z. Cai,et al.  Gossypol repressed the gap junctional intercellular communication between Sertoli cells by decreasing the expression of Connexin43. , 2008, Toxicology in vitro : an international journal published in association with BIBRA.

[43]  D. Cyr,et al.  Nonylphenol Alters Connexin 43 Levels and Connexin 43 Phosphorylation Via an Inhibition of the p38-Mitogen-Activated Protein Kinase Pathway1 , 2005, Biology of reproduction.