Quercetin-Loaded Avocado Oil Nanoemulsion Reverses High-fat and High-carbohydrate Diet-Induced Testicular Dysfunction: Role of Oxidative Stress and NPY Signaling in a Randomized Trial.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2025-12-31 eCollection Date: 2025-01-01 DOI:10.5812/ijpr-165025
Hamidreza Mazangi, Negar Panahi, Saeed Hesaraki, Shahabeddin Safi
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引用次数: 0

Abstract

Background: High-fat and high-carbohydrate diets (HF) can negatively affect male reproductive function, impairing spermatogenesis and testosterone production. Quercetin (Qu) may mitigate testicular damage, but its effectiveness is limited by poor bioavailability. Avocado oil (AO) improves blood lipid levels and enhances the absorption of fat-soluble nutrients.

Objectives: We explore the impact of AO combined with quercetin on weight gain, dyslipidemia, hormonal dysregulation, testicular oxidative stress, and NPY signaling, all induced by a HF diet, to highlight testicular dysfunction and metabolic disorders.

Methods: A nanoemulsion of avocado oil containing quercetin (NAOQu) was developed as an oil-in-water (O/W) nanoemulsion, utilizing the hydrophilic-lipophilic balance (HLB) value and conducting stability assessments, followed by characterization (DLS, Zeta potential, and TEM). Thirty rats were fed an HF diet for 8 weeks and treated with either Qu, a nanoemulsion of avocado oil (NAO), or NAOQu. Body weight was determined, and serum was analyzed for triglycerides (TG), cholesterol, HDL, and testosterone levels. Testicular homogenates were assessed for malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD) activity, and cholesterol. Hypothalamic NPY mRNA expression was quantified using qPCR.

Results: The NAOQu (1% Qu, 1:1 avocado: Coconut oil) exhibited a stable, spherical morphology with a particle size of 286.7 nm, a zeta potential of -25.8 mV, and enhanced physical stability. The NAOQu significantly reduced body weight, improved lipid profiles (lowering TG and cholesterol while increasing HDL), and restored testosterone levels by 85% compared to high-fat diet (HFD) controls and reduced testicular MDA by 62% while increasing GSH and SOD activities by 2.3-fold and 1.8-fold, respectively. Molecular analyses revealed decreased testicular cholesterol levels and downregulated NPY mRNA expression, indicating reduced metabolic stress.

Conclusions: The combined NAOQu formulation showed greater protective effects than Qu or AO alone, suggesting a synergistic effect. These findings highlight the potential of avocado oil-based nanoemulsion as an effective delivery system for Qu, offering a novel therapeutic strategy to counteract HF-induced male reproductive dysfunction and metabolic disease.

负载槲皮素的鳄梨油纳米乳逆转高脂肪和高碳水化合物饮食诱导的睾丸功能障碍:氧化应激和NPY信号的作用在一项随机试验中
背景:高脂肪和高碳水化合物饮食会对男性生殖功能产生负面影响,损害精子发生和睾丸激素的产生。槲皮素(Qu)可以减轻睾丸损伤,但其有效性受到生物利用度差的限制。鳄梨油(AO)改善血脂水平,增强脂溶性营养素的吸收。目的:我们探讨AO联合槲皮素对HF饮食诱导的体重增加、血脂异常、激素失调、睾丸氧化应激和NPY信号的影响,以突出睾丸功能障碍和代谢紊乱。方法:制备含槲皮素(NAOQu)的牛油果油水包油(O/W)纳米乳,利用亲水-亲脂平衡(HLB)值进行稳定性评价,并进行DLS、Zeta电位和TEM表征。30只大鼠饲喂HF饮食8周,然后分别用牛油果油纳米乳(NAO)或牛油果油纳米乳(NAOQu)治疗。测定体重,分析血清甘油三酯(TG)、胆固醇、高密度脂蛋白和睾酮水平。评估睾丸匀浆的丙二醛(MDA)、谷胱甘肽(GSH)、超氧化物歧化酶(SOD)活性和胆固醇。采用qPCR定量检测下丘脑NPY mRNA的表达。结果:NAOQu (1% Qu, 1:1鳄梨:椰子油)具有稳定的球形形貌,粒径为286.7 nm, zeta电位为-25.8 mV,物理稳定性增强。与高脂饮食(HFD)对照组相比,NAOQu显著降低了体重,改善了脂质谱(降低TG和胆固醇,同时增加HDL),恢复了85%的睾丸激素水平,降低了62%的睾丸MDA,提高了2.3倍和1.8倍的GSH和SOD活性。分子分析显示睾丸胆固醇水平降低,NPY mRNA表达下调,表明代谢应激减轻。结论:NAOQu联合制剂的保护作用明显优于单用Qu或AO,具有协同作用。这些发现突出了牛油果油纳米乳作为一种有效的曲曲醇递送系统的潜力,为对抗hf诱导的男性生殖功能障碍和代谢疾病提供了一种新的治疗策略。
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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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