雌性小鼠肥胖相关的高尿酸血症:重新评估。

Gout, urate, and crystal deposition disease Pub Date : 2024-09-01 Epub Date: 2024-08-30 DOI:10.3390/gucdd2030019
Andrew P Giromini, Sonia R Salvatore, Brooke A Maxwell, Sara E Lewis, Michael R Gunther, Marco Fazzari, Francisco J Schopfer, Roberta Leonardi, Eric E Kelley
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引用次数: 0

摘要

许多临床前报告一致认为,肥胖与组织中尿酸(UA)水平升高之间存在密切联系,尤其是在血液循环中(高尿酸血症)。不幸的是,几乎所有这些研究都是在雄性老鼠身上进行的,在一个案例中,雌性老鼠没有并排的雄性队列。因此,雌性小鼠肥胖与高尿酸血症之间的关系尚不明确。由于肥胖和相关高尿酸血症的下游影响广泛,导致许多合并症,包括心血管功能障碍、慢性肾脏疾病和非酒精性脂肪性肝病(NAFLD),因此该领域缺乏清晰度具有相当大的影响。在此,我们开始通过在一项男女C57BL/6J对照研究中揭示饮食性肥胖(DIO)的表型和代谢反应来解决这个问题。从6周龄开始,小鼠被暴露在致肥性饮食(60%的热量来自脂肪)或对照饮食(10%的热量来自脂肪)中19周。与许多报道的60%饮食观察结果相似,与年龄匹配的瘦雄性对照组(1.53±0.19 mg/dL)相比,雄性小鼠随着时间的推移体重显著增加,空腹血糖升高,葡萄糖耐量受损,循环尿酸水平显著升高(2.54±0.33 mg/dL)。不出所料,与雄性小鼠相比,雌性小鼠的体重增长速度较慢;然而,与年龄匹配的瘦对照组相比,他们也出现了空腹血糖升高和葡萄糖耐量下降。与我们之前的报告相反,雌性研究的对照饮食是体内标准食物(18%的热量来自脂肪),肥胖雌性小鼠的循环UA水平(2.55±0.15 mg/dL)明显高于正常对照组(1.68±0.12 mg/dL)。这证实了控制饮食的选择是得出持久结论的关键。综上所述,这些结果首次揭示了循环尿酸升高是男性和女性对致肥性喂养的类似长期反应,并反映了临床观察显示的两性肥胖的高尿酸血症。
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Obesity-Associated Hyperuricemia in Female Mice: A Reevaluation.

Many preclinical reports have coalesced to identify a strong association between obesity and increased levels of uric acid (UA) in tissues and, importantly in the circulation (hyperuricemia). Unfortunately, nearly all these studies were conducted with male mice or, in one case, female mice without a side-by-side male cohort. Therefore, the relationship between obesity and hyperuricemia in female mice remains undefined. This lack of clarity in the field has considerable impact as the downstream effects of obesity and allied hyperuricemia are extensive, resulting in many comorbidities including cardiovascular dysfunction, chronic kidney disease and nonalcoholic fatty liver disease (NAFLD). Herein we begin to address this issue by revealing phenotypic and metabolic responses to diet-induced obesity (DIO) in a side-by-side male vs. female C57BL/6J study. Beginning at 6 weeks of age, mice were exposed to either an obesogenic diet (60% calories from fat) or control diet (10% calories from fat) for 19 weeks. Similar to numerous reported observations with the 60% diet, male mice experienced significant weight gain over time, elevated fasting blood glucose, impaired glucose tolerance and significantly elevated circulating uric acid levels (2.54 ± 0.33 mg/dL) compared to age-matched lean male controls (1.53 ± 0.19 mg/dL). As expected, the female mice experienced a slower rate of weight gain compared to the males; however, they also developed elevated fasting blood glucose and impaired glucose tolerance compared to age-matched lean controls. Countervailing our previous report whereby the control diet for the female-only study was vivarium standard chow (18% calories from fat), the obese female mice did demonstrate significantly elevated circulating UA levels (2.55 ± 0.15 mg/dL) compared to the proper control (1.68 ± 0.12 mg/dL). This affirms that the choice of control diet is crucial for reaching durable conclusions. In toto, these results, for the first time, reveal elevated circulating UA to be a similar long-term response to obesogenic feeding for both males and females and mirrors clinical observations demonstrating hyperuricemia in obesity for both sexes.

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Effect of Allopurinol Use on Kidney Function Among Patients with Gout and Chronic Kidney Disease. A Novel Polarized Light Microscope for the Examination of Birefringent Crystals in Synovial Fluid. Obesity-Associated Hyperuricemia in Female Mice: A Reevaluation.
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