Melatonin protect against pregabalin-induced gonadotoxicity via anti-oxidative, anti-inflammatory, anti-apoptotic, enzymatic and hormonal regulatory mechanisms in rats.

IF 2.7 3区 医学 Q2 PHARMACOLOGY & PHARMACY BMC Pharmacology & Toxicology Pub Date : 2025-02-12 DOI:10.1186/s40360-025-00863-w
Ayodeji Folorunsho Ajayi, Motolani Susan Borisade, Precious Oyedokun, Oyedayo Phillips Akano, Lydia Oluwatoyin Ajayi, David Tolulope Oluwole, Wale Johnson Adeyemi
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Abstract

Background: The therapeutic value of pregabalin in managing various pathological states, such as sleep, anxiety, and bipolar disorders, fibromyalgia, epilepsy, and others, cannot be overstated. Nevertheless, the gonadotoxicity of this drug remains a concern. In contrast, melatonin, an endogenous hormone, is known for its beneficial effects on reproductive tissues following various insults. Thus, this study aimed to examine the impact of melatonin on male Wistar rats exposed to pregabalin.

Methods: A total of sixty male Wistar rats, weighing between 120 and 140 g, were randomly assigned to six groups, with each group consisting of ten rats. The control group was given 0.5 ml of normal saline orally, whereas melatonin was administered alone at 10 mg/kg/BW, and pregabalin was delivered at low and high doses of 150 and 300 mg/kg/BW orally, respectively. At the specified dosages, rats were also treated simultaneously with low and high doses of pregabalin in combination with melatonin. All treatments lasted for 56 days. Biomarkers were assayed in the testicular and epididymal tissues, while hormones were assayed in the serum.

Results: Pregabalin treatment resulted in notable decreases in the percentage body weight change, testicular weight, relative testicular weight, FSH, LH, testosterone, 3β-HSD, 17β-HSD, SOD, catalase, and GSH, as compared to the control group. However, these effects were mitigated in the groups administered melatonin in conjunction with pregabalin. Pregabalin treatment also caused significant elevations in lactate, pyruvate, LDH, GGT, MDA, caspase, IL-1β, NF-κB, and TNF-α, and distorted testicular histoarchitecture, but these effects were blunted in the group co-administered with pregabalin and melatonin. The histological findings paralleled the biochemical assays.

Conclusion: Conclusively, melatonin has a protective effect against pregabalin-induced gonadotoxicity through anti-oxidative, anti-inflammatory, anti-apoptotic, enzymatic, and hormonal regulatory mechanisms.

Clinical trial number: Not applicable.

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褪黑素通过抗氧化、抗炎、抗凋亡、酶和激素调节机制保护大鼠免受普瑞巴林诱导的促性腺毒性。
背景:普瑞巴林在控制各种病理状态,如睡眠、焦虑、双相情感障碍、纤维肌痛、癫痫等方面的治疗价值不能被夸大。然而,这种药物的促性腺毒性仍然令人担忧。相反,褪黑素是一种内源性激素,在各种损伤后对生殖组织有有益作用。因此,本研究旨在研究褪黑素对普瑞巴林暴露的雄性Wistar大鼠的影响。方法:选用体重120 ~ 140 g的雄性Wistar大鼠60只,随机分为6组,每组10只。对照组给予生理盐水0.5 ml口服,褪黑素单独给予10 mg/kg/BW,普瑞巴林分别口服低剂量和高剂量150和300 mg/kg/BW。在指定剂量下,大鼠也同时接受低剂量和高剂量普瑞巴林与褪黑激素联合治疗。所有治疗持续56 d。在睾丸和附睾组织中检测生物标志物,在血清中检测激素。结果:与对照组相比,普瑞巴林治疗组体重变化率、睾丸质量、相对睾丸质量、FSH、LH、睾酮、3β-HSD、17β-HSD、SOD、过氧化氢酶、GSH均显著降低。然而,在服用褪黑素和普瑞巴林的组中,这些影响有所减轻。普瑞巴林治疗也引起乳酸、丙酮酸、LDH、GGT、MDA、caspase、IL-1β、NF-κB和TNF-α显著升高,睾丸组织结构扭曲,但普瑞巴林和褪黑激素联合使用组这些影响减弱。组织学结果与生化分析一致。结论:褪黑素通过抗氧化、抗炎、抗凋亡、酶和激素调节机制对普瑞巴林诱导的促性腺毒性具有保护作用。临床试验号:不适用。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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