Alpha-pinene neutralizes cisplatin-induced reproductive toxicity in male rats through activation of Nrf2 pathway

被引:6
|
作者
Demir, Selim [1 ]
Mentese, Ahmet [2 ]
Usta, Zeynep Turkmen [3 ]
Alemdar, Nihal Turkmen [4 ,5 ]
Demir, Elif Ayazoglu [6 ]
Aliyazicioglu, Yuksel [2 ]
机构
[1] Karadeniz Tech Univ, Fac Hlth Sci, Dept Nutr & Dietet, TR-61080 Trabzon, Turkiye
[2] Karadeniz Tech Univ, Fac Med, Dept Med Biochem, TR-61080 Trabzon, Turkiye
[3] Karadeniz Tech Univ, Fac Med, Dept Med Pathol, TR-61080 Trabzon, Turkiye
[4] Karadeniz Tech Univ, Grad Sch Hlth Sci, Dept Med Biochem, TR-61080 Trabzon, Turkiye
[5] Recep Tayyip Erdogan Univ, Vocat Sch Hlth Serv, Dept Med Serv & Tech, TR-53100 Rize, Turkiye
[6] Karadeniz Tech Univ, Macka Vocat Sch, Dept Chem & Chem Proc Technol, TR-61750 Trabzon, Turkiye
关键词
Alpha-pinene; Cisplatin; Endoplasmic reticulum stress; Inflammation; Nrf2; Oxidative stress; ENDOPLASMIC-RETICULUM STRESS; OXIDATIVE STRESS; SUPPRESSION; APOPTOSIS; DAMAGES; INJURY;
D O I
10.1007/s11255-023-03817-5
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
PurposeTesticular toxicity is one of the most important side effects of cisplatin (CP) therapy. Alpha-pinene (AP) is a naturally occurring monoterpene with antioxidant character in plants. Here, we aimed to evaluate the therapeutic activity of AP against CP-induced testicular toxicity by including the nuclear factor erythroid 2-associated factor 2 (Nrf2) pathway in rats.MethodsThirty male rats were divided into 5 groups: control, CP, CP + AP (5 and 10 mg/kg) and only AP (10 mg/kg). CP was administered intraperitoneally at a dose of 5 mg/kg on the first day, followed by three consecutive injections of AP. Serum reproductive hormone levels were evaluated using ELISA kits. Oxidative stress (OS), inflammation, endoplasmic reticulum stress (ERS) and apoptosis markers in testicular tissue were also determined colorimetrically. In addition, how CP affects Nrf2 pathway and the effect of AP on this situation were also addressed.ResultsTreatment with CP significantly increased OS, inflammation, ERS and apoptosis in testicular tissue. Administrations of AP resulted in an amelioration of these altered parameters. The mechanism of therapeutic effect of AP appeared to involve induction of Nrf2. Furthermore, these results were also confirmed by histological data.ConclusionResults suggest that AP can exhibit therapeutic effects against CP-induced testicular toxicity. It can be concluded that AP may be a potential molecule to abolish reproductive toxicity after chemotherapy.
引用
收藏
页码:527 / 537
页数:11
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