Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion

被引:21
作者
Dhulqarnain, Akanji Omotosho [1 ]
Takzaree, Nasrin [1 ,2 ]
Hassanzadeh, Golamreza [1 ,2 ]
Tooli, Heidar [3 ,5 ]
Malekzadeh, Mehrnoush [2 ]
Khanmohammadi, Nasrin [2 ]
Yaghobinejad, Mahsa [2 ]
Solhjoo, Somayeh [4 ]
Rastegar, Tayebeh [1 ,2 ]
机构
[1] Univ Tehran Med Sci, Dept Anat, Sch Med, Int Campus, Tehran, Iran
[2] Univ Tehran Med Sci, Sch Med, Dept Anat, Tehran, Iran
[3] Shahroud Univ Med Sci, Sch Med, Dept Anat, Sharoud, Iran
[4] Kerman Univ Med Sci, Dept Anat, Kerman, Iran
[5] Shahroud Univ Med Sci, Tissue Engn & Stem Cells Res Ctr, Shahroud, Iran
关键词
Pentoxifylline; Testicular torsion-detorsion; Spermatogenesis; Oxidative stress; Antioxidant; PI3K/AKT pathway; Apoptosis; ISCHEMIA-REPERFUSION INJURY; ID PROTEINS; BLOOD-FLOW; GERM-CELLS; APOPTOSIS; ANTIOXIDANT; EXPRESSION; ACTIVATION; INHIBITOR; THERAPY;
D O I
10.1016/j.heliyon.2021.e06868
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Testicular torsion-detorsion results in enhanced formation of free radicals which contribute to the pathophysiology of testicular tissue damage. Recent reports have identified protective role of pentoxifylline (PTX) against free radicals. Thus, we determined the protective effect of pentoxifylline against testicular damage in mouse model of testicular torsion-detorsion. Twenty (6 weeks old) male mice were divided into 4 groups of 5 animals each namely: Control (sham operated group), T1 (Torsion-detosion thorn single dose 100 mg/kg PTX, T2 (torsion-detorsion thorn 20 mg/kg PTX for 2 weeks and T/D (torsion-detorsion only). Animals in T1, T2 and T/D groups underwent 2 h of testicular torsion with the left testes rotated 720 degrees (clockwisely) followed by 30 min of detorsion. After detorsion, drug administration was done intraperitoneally. The left testes of all the animals were excised on the 35th day after torsion-detortion for histopathological and biochemical assay. Histomorphological analysis of the seminiferous tubules showed that there were significant increase (P < 0.01 or 0.05) in the mean seminiferous tubule diameter, Johnson score and germ cells of animals in Control and T1 compared to T2 and T/D with no significant difference (P > 0.05) in testes weight, sertoli, leydig and myoid cells in all groups. IHC results showed significant increase (P < 0.01 or 0.05) in id4 and scp3 protein markers in Control, T1 and T2 compared to T/D. Oxidative stress analysis revealed that Pentoxifylline significantly increased (P < 0.01 or 0.05) the level of SOD, catalase, mRNA expression of akt and pi3k genes but significantly suppress (P < 0.01 or 0.05) MDA and Caspase-3 level in Control, T1 and T2 compared to T/D. Pentoxifylline could be used as an adjunct therapy to surgery in the treatment of torsion-detorsion related testicular injury, However, Further studies are needed to evaluate the effects of pentoxifylline on testicular torsion.
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页数:11
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