Mitigation of radiation injury to reproductive system of male mice by Trichostatin A

曲古抑菌素A 微核试验 生物 DNA损伤 基因组不稳定性 细胞凋亡 组蛋白脱乙酰基酶 遗传毒性 精子发生 微核 男科 DNA修复 不育 癌症研究 毒理 遗传学 组蛋白 毒性 内科学 医学 内分泌学 DNA
作者
Teena Haritwal,Namita Kalra,Paban K. Agrawala
出处
期刊:Mutation Research [Elsevier]
卷期号:881: 503522-503522 被引量:1
标识
DOI:10.1016/j.mrgentox.2022.503522
摘要

Trichostatin A (TSA), derived from the bacteria Streptomyces hygroscopicus, is a hydroxamic acid having various biological properties such as histone deacetylase inhibition, anticancer and radiomitigative action. However the mitigative activity of TSA against radiation-induced damages in the mouse reproductive system has not yet been elucidated. The present study unraveled the effects of 2 Gy whole body irradiation (60Co γ- radiation) on C57BL/6 mice male reproductive system including structural damages to testes, increase in apoptosis and reduction in germ cell viability, reduced fertility as well as increased genomic instability in the next generation. Moreover, hematological study and micronuclei assay were used to record chances of radiation-induced hematologic cancer and disruption of genomic integrity in F1 generation. Interestingly, TSA administration 1 and 24 h post-irradiation attenuated radiation-induced morphological damage and cellular apoptosis in testes. In male mice, TSA restored hematological parameters and micronuclei frequency to normal levels, restored sperm viability, and helped them overcome radiation-induced temporary sterility 5 weeks after the irradiation. Thus our results showed that TSA reduced the probability of radiation-induced hematologic cancers as well as genotoxicity and restored genomic integrity in the progenies of paternally exposed mice by reducing radiation-induced apoptosis in spermatogenic cells and restoring cell proliferation. This study suggested that TSA could be used as potential radiomitigator for male reproductive system.
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