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饮食诱导肥胖导致 CBA/Ca 小鼠听力损伤的性别差异。

Sex differences in hearing impairment due to diet-induced obesity in CBA/Ca mice.

机构信息

Brain Research Institute, College of Medicine, Chungnam National University, 282 Munwha-ro, Daesa-dong, Jung-gu, 35015, Daejeon, South Korea.

Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, 35015, South Korea.

出版信息

Biol Sex Differ. 2023 Feb 21;14(1):10. doi: 10.1186/s13293-023-00493-z.

Abstract

BACKGROUND

Obesity is an independent risk factor for hearing loss. Although attention has focused on major obesity comorbidities such as cardiovascular disease, stroke, and type 2 diabetes, the impact of obesity on sensorineural organs, including the auditory system, is unclear. Using a high-fat diet (HFD)-induced obese mouse model, we investigated the impact of diet-induced obesity on sexual dimorphism in metabolic alterations and hearing sensitivity.

METHODS

Male and female CBA/Ca mice were randomly assigned to three diet groups and fed, from weaning (at 28 days) to 14 weeks of age, a sucrose-matched control diet (10 kcal% fat content diet), or one of two HFDs (45 or 60 kcal% fat content diets). Auditory sensitivity was evaluated based on the auditory brainstem response (ABR), distortion product otoacoustic emission (DPOAE), and ABR wave 1 amplitude at 14 weeks of age, followed by biochemical analyses.

RESULTS

We found significant sexual dimorphism in HFD-induced metabolic alterations and obesity-related hearing loss. Male mice exhibited greater weight gain, hyperglycemia, increased ABR thresholds at low frequencies, elevated DPOAE, and lower ABR wave 1 amplitude compared to female mice. The hair cell (HC) ribbon synapse (CtBP2) puncta showed significant sex differences. The serum concentration of adiponectin, an otoprotective adipokine, was significantly higher in female than in male mice; cochlear adiponectin levels were elevated by HFD in female but not male mice. Adiponectin receptor 1 (AdipoR1) was widely expressed in the inner ear, and cochlear AdipoR1 protein levels were increased by HFD, in female but not male mice. Stress granules (G3BP1) were significantly induced by the HFD in both sexes; conversely, inflammatory (IL-1β) responses were observed only in the male liver and cochlea, consistent with phenotype HFD-induced obesity.

CONCLUSIONS

Female mice are more resistant to the negative effects of an HFD on body weight, metabolism, and hearing. Females showed increased peripheral and intra-cochlear adiponectin and AdipoR1 levels, and HC ribbon synapses. These changes may mediate resistance to HFD-induced hearing loss seen in female mice.

摘要

背景

肥胖是听力损失的一个独立危险因素。尽管人们已经关注到肥胖的主要合并症,如心血管疾病、中风和 2 型糖尿病,但肥胖对包括听觉系统在内的感觉神经器官的影响尚不清楚。本研究使用高脂肪饮食(HFD)诱导肥胖的小鼠模型,研究了饮食诱导的肥胖对代谢改变和听力敏感性的性别二态性的影响。

方法

雄性和雌性 CBA/Ca 小鼠被随机分配到三组饮食组中,并从断奶(28 天)到 14 周龄时,喂食蔗糖匹配的对照饮食(10 kcal%脂肪含量饮食)或两种 HFD(45 或 60 kcal%脂肪含量饮食)。在 14 周龄时,根据听性脑干反应(ABR)、畸变产物耳声发射(DPOAE)和 ABR 波 1 幅度评估听觉敏感性,然后进行生化分析。

结果

我们发现 HFD 诱导的代谢改变和肥胖相关听力损失存在显著的性别二态性。与雌性小鼠相比,雄性小鼠体重增加更多、血糖升高、低频 ABR 阈值升高、DPOAE 升高、ABR 波 1 幅度降低。毛细胞(HC) ribbon synapse(CtBP2) puncta 显示出显著的性别差异。血清脂联素浓度,一种保护性的脂肪因子,在雌性小鼠中明显高于雄性小鼠;HFD 可使雌性小鼠耳蜗脂联素水平升高,但不能使雄性小鼠耳蜗脂联素水平升高。脂联素受体 1(AdipoR1)在内耳广泛表达,HFD 可使雌性小鼠而非雄性小鼠的耳蜗 AdipoR1 蛋白水平升高。应激颗粒(G3BP1)在两性中均被 HFD 显著诱导;相反,炎症(IL-1β)反应仅在雄性肝脏和耳蜗中观察到,与 HFD 诱导的肥胖表型一致。

结论

雌性小鼠对 HFD 对体重、代谢和听力的负面影响更具抵抗力。雌性小鼠外周和耳蜗内脂联素和 AdipoR1 水平以及 HC ribbon synapses 增加。这些变化可能介导了雌性小鼠对 HFD 诱导的听力损失的抵抗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4340/9945383/323e50e224cf/13293_2023_493_Fig1_HTML.jpg

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