睾丸内的粘蛋白抑制会破坏小鼠睾丸中的雄激素和雌激素信号。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-09-28 DOI:10.1016/j.repbio.2024.100956
Vanlal Rempuia, Guruswami Gurusubramanian, Vikas Kumar Roy
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引用次数: 0

摘要

Visfatin在鸡、人和啮齿类动物的睾丸中均有表达,但Visfatin在成人睾丸中的直接作用尚未得到研究。我们研究了睾丸内注射 FK866 后睾丸的反应。我们在 FK866 治疗后 24 小时和一周内分别检测了抑制粘蛋白的效果。FK866 治疗 24 小时后,睾丸组织结构退化,睾酮和增殖标志物受抑制,1 周后这些指标恢复。FK866 处理 1 周后,AR 和 ERα 的表达下调。24 小时后,BCl2 的表达下调,caspase3 的表达略有升高;但一周后,这两种蛋白的表达仍受到抑制。此外,与对照组相比,两组的 ERβ 表达、3βHSD 和 17βHSD 均出现下调。尽管某些因子被下调,但睾丸的增殖和组织结构在FK866治疗1周后出现恢复。这可能是由于芳香化酶的表达受到抑制,从而增加了睾酮的分泌。总之,我们的研究结果是首次报道粘蛋白在成人睾丸中的直接作用。Visfatin对睾丸中睾酮的合成和增殖具有刺激作用。此外,尽管组织结构处理正常,但在FK866治疗1周后,睾丸中的一些因子出现了失调,这可能是粘蛋白抑制后的一种代偿机制。
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Intra-testicular visfatin inhibition disrupts androgen and estrogen signalling in the mouse testis
Visfatin is expressed in the testis of chicken, humans and rodents; however, direct role of visfatin in the adult testis has not been studied. We investigated testicular responses after intra-testicular injection of FK866. The effects of visfatin inhibition were accessed at 24 hrs and 1 week post FK866 treatment. The testicular histoarchitecture were degenerated after 24 hrs of FK866 treatment along with supressed testosterone and proliferating markers and resumption in these parameters showed after 1 week. The expression of AR and ERα were down-regulated after 1 week of FK866 treatment. The expression of BCl2 was down-regulated along with a slight elevation of caspase3 after 24 hrs; however, both proteins still showed suppressed expression after 1 week. Furthermore, ERβ expression, 3βHSD, and 17βHSD were down-regulated in both groups compared to the control. Despite the down-regulation of some factors, the testicular proliferation and histoarchitecture showed resumption in the testis after 1 week of FK866 treatment. This could be due to increased testosterone secretion by suppressing aromatase expression. In conclusion, our result is the first report on the direct role of visfatin in the adult testis. Visfatin has a stimulatory role in testosterone synthesis and proliferation in the testis. Moreover, some deregulated factors in the testis after 1 week of FK866 treatment, despite normal histoarchitecture treatment, could be a compensatory mechanism after visfatin inhibitions.
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ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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