Honokiol Attenuates Torsion/Detorsion-induced Testicular Injury in Rat Testis by Way of Suppressing Endoplasmic Reticulum Stress-related Apoptosis

被引:31
|
作者
Huang, Kuo-How
Weng, Te-I
Huang, Hsin-Yi
Huang, Kuo-Dong
Lin, Wei-Chou
Chen, Shyh-Chyan
Liu, Shing-Hwa [1 ]
机构
[1] Natl Taiwan Univ, Inst Toxicol, Coll Med, Taipei 10051, Taiwan
关键词
ISCHEMIA-REPERFUSION INJURY; UNFOLDED PROTEIN RESPONSE; OXYGEN SPECIES PRODUCTION; CEREBRAL-ISCHEMIA; TORSION; BRAIN; PERK; ACTIVATION; MECHANISMS; SALVAGE;
D O I
10.1016/j.urology.2011.11.027
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To investigate the protective effect of honokiol, a phytochemical used in traditional medicine, on testicular injury after torsion/detorsion (T/D) in a rat model. Testicular torsion is a medical emergency that can cause impairment of semen quality and permanent testicular atrophy or loss. METHODS Male Wistar rats were randomized to each time point of each group (n = 6/time point/group). After 2 hours of torsion, the testes were counter-rotated to the natural position. The rats in each group underwent a sham operation, T/D, or T/D with honokiol treatment (5 mg/kg and 10 mg/kg intraperitoneally, immediately before detorsion). Bilateral orchiectomy was performed at 6 and 24 hours and 3 months after detorsion. The testes were examined histologically. Apoptosis and endoplasmic reticulum stress were detected by Western blot. RESULTS Histologic examination revealed that testicular T/D induced acute injury after 6 and 24 hours, and spermatogenesis was decreased at 3 months of follow-up. At 24 hours after T/D, increases were found in the activation of apoptosis-related molecules [poly (ADP-ribose) polymerase and caspases 3 and 7], and the expression levels of endoplasmic reticulum stress-associated molecules (phosphorylated-eukaryotic translation initiation factor 2 subunit alpha and CCAAT/enhancerbinding protein homologous protein). These increases were significantly reversed with honokiol treatment. Furthermore, honokiol effectively reversed the inhibition of spermatogenesis in testes treated with T/D for 3 months. CONCLUSION The results of our study have shown that the endoplasmic reticulum stress-related apoptotic pathway is involved in testicular injury after testicular T/D. It remains to be determined whether alterations in this pathway would have a protective affect against reperfusion damage. UROLOGY 79: 967.e5-967.e11, 2012. (C) 2012 Elsevier Inc.
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