奥利多宁对精子功能和 PI3K/PDK1/AKT 信号通路的影响:对生殖毒性的影响。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY
Ju-Mi Hwang , Woo-Jin Lee , Jae-Hwan Jo , Claudine Uwamahoro , Seung-Ik Jang , Eun-Ju Jung , Jeong-Won Bae , Dae-Hyun Kim , Jun Koo Yi , Jae Jung Ha , Dong Yep Oh , Woo-Sung Kwon
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引用次数: 0

摘要

Oridonin 是一种从 Isodon rubescens (Hemsley) H.Hara 的叶子中分离出来的天然萜类化合物,因其在各种癌症类型中的抗癌特性而被广泛应用于东方医学中。尽管它被广泛使用,但人们对其对男性生殖系统的毒性作用,尤其是对精子功能的影响及其机制还不甚了解。本研究旨在探索奥利多宁对精子功能的影响及其内在机制。我们首先用不同浓度的奥利多宁(0、5、50、75、100 和 150µM)处理杜洛克公猪精子,并将其培养以诱导获能。然后,我们评估了细胞存活率和精子的几种功能,包括精子运动和运动学、获能状态和 ATP 水平。我们还分析了与磷脂酰肌醇-3-激酶(PI3K)/磷脂酰肌醇依赖性激酶-1(PDK1)/蛋白激酶 B(AKT)信号通路相关的蛋白质和磷酸酪氨酸蛋白的表达水平。我们的研究结果表明,奥利多宁以剂量依赖的方式对大多数精子功能产生不利影响。我们观察到,奥利多宁治疗后,AKT、p-AKT (Thr308)、磷酸酶和天丝蛋白同源物(PTEN)、p-PDK1 和 p-PI3K 水平明显下降,同时磷酸酪氨酸蛋白异常增加。这些研究结果表明,奥利多宁可能会通过抑制 PI3K/PDK1/AKT 信号通路来破坏酪氨酸磷酸化蛋白的正常水平,而 PI3K/PDK1/AKT 信号通路对细胞增殖、新陈代谢和凋亡至关重要,因此可能会损害精子功能。因此,我们建议在将奥利多宁用作治疗药物时考虑其生殖毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of oridonin on sperm function and the PI3K/PDK1/AKT signaling pathway: Implications for reproductive toxicity

Oridonin, a natural terpenoid isolated from the leaves of Isodon rubescens (Hemsley) H.Hara, is widely used in oriental medicine for its anticancer properties across various cancer types. Despite its prevalent use, the toxic effects of oridonin on male reproduction, particularly its impact on sperm functions and the mechanisms involved, are not well understood. This study aimed to explore the effects and underlying mechanisms of oridonin on sperm functions. We initially treated Duroc boar spermatozoa with varying concentrations of oridonin (0, 5, 50, 75, 100, and 150 µM) and incubated them to induce capacitation. We then assessed cell viability and several sperm functions, including sperm motility and motion kinematics, capacitation status, and ATP levels. We also analyzed the expression levels of proteins associated with the phosphatidylinositol 3-kinase (PI3K)/phosphoinositide-dependent kinase-1 (PDK1)/protein kinase B (AKT) signaling pathway and phosphotyrosine proteins. Our results indicate that oridonin adversely affects most sperm functions in a dose-dependent manner. We observed significant decreases in AKT, p-AKT (Thr308), phosphatase and tensin homolog (PTEN), p-PDK1, and p-PI3K levels following oridonin treatment, alongside an abnormal increase in phosphotyrosine proteins. These findings suggest that oridonin may disrupt normal levels of tyrosine-phosphorylated proteins by inhibiting the PI3K/PDK1/AKT signaling pathway, which is crucial for cell proliferation, metabolism, and apoptosis, thus potentially harming sperm functions. Consequently, we recommend considering the reproductive toxicity of oridonin when using it as a therapeutic agent.

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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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