Kianifard Davoud, Shoar Seyyed Maysam Mousavi, Karkan Morteza Fallah, Aly Ahmed
Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, Iran.
Department of Basic Sciences, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Int J Reprod Biomed. 2021 Feb 21;19(2):167-180. doi: 10.18502/ijrm.v19i2.8475. eCollection 2021 Feb.
Quinine (QU) as an anti-malarial drug induces alterations in testicular tissue. Toxic effects of monosodium glutamate (MSG) on the male reproductive system have been recognized.
To investigate the impact of MSG administration on the intensity of gonadotoxicity of QU.
Sixty eight-wk old Wistar rats weighing 180-200 gr were divided into six groups (n = 10/each): the first group as a control; the second and third groups received low and high doses of MSG (2 & 4 gr/kg i.p.), respectively, for 28 days; the fourth group received QU for seven days (25 mg/kg); and in the fifth and sixth groups, QU was gavaged following the MSG administration (MSG + QU) from day 22 to day 28. Serum testosterone and malondialdehyde (MDA) levels were measured. Testes samples were prepared for tissue MDA levels, histomorphometry, and immunohistochemistry of p53. Sperm analysis was performed on cauda epididymis.
Serum and tissue MDA levels were increased in treated groups compared to the control group. This increment was higher in the MSG + QU groups. The testosterone levels were reduced significantly (p 0.0001) in all treated groups. In addition, histomorphometric indices and tubular epithelium population were reduced significantly (p 0.0001) in QU, MSG + QU, and consequently in high-dose MSG, QU, MSG + QU groups. All spermatogenic indices were reduced in the treated groups, particularly in the MSG + QU groups. Sperm motility and viability indices were reduced significantly (p = 0.003) in the MSG + QU groups. Finally, the overexpression of p53 was observed in the MSG + QU groups.
The administration of MSG before and during QU therapy may intensify testicular tissue alterations.
奎宁(QU)作为一种抗疟药物会引起睾丸组织的改变。味精(MSG)对雄性生殖系统的毒性作用已得到认可。
研究给予味精对奎宁性腺毒性强度的影响。
将60只8周龄、体重180 - 200克的Wistar大鼠分为六组(每组n = 10):第一组为对照组;第二组和第三组分别接受低剂量和高剂量的味精(2克/千克和4克/千克腹腔注射),持续28天;第四组接受奎宁治疗7天(25毫克/千克);第五组和第六组在第22天至第28天给予味精后灌胃奎宁(味精 + 奎宁)。检测血清睾酮和丙二醛(MDA)水平。制备睾丸样本用于检测组织MDA水平、组织形态计量学以及p53的免疫组织化学分析。对附睾尾部进行精子分析。
与对照组相比,各治疗组血清和组织MDA水平均升高。在味精 + 奎宁组中这种升高更为明显。所有治疗组的睾酮水平均显著降低(p < 0.0001)。此外,在奎宁组、味精 + 奎宁组以及高剂量味精、奎宁、味精 + 奎宁组中,组织形态计量学指标和肾小管上皮细胞数量均显著减少(p < 0.0001)。所有生精指标在各治疗组中均降低,尤其是在味精 + 奎宁组。味精 + 奎宁组的精子活力和存活率指标显著降低(p = 0.003)。最后,在味精 + 奎宁组中观察到p53的过表达。
在奎宁治疗前及治疗期间给予味精可能会加剧睾丸组织的改变。