Evaluation of the hepatic and subcutaneous adipose tissue effects of triiodothyronine treatment in an animal model of metabolic syndrome.

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Marta Borges-Canha, Ana Rita Leite, Glória Conceição, Catarina Vale, Madalena Von-Hafe, Diana Martins, Daniela Miranda-Silva, Cláudia Sousa-Mendes, Joana Chaves, Inês Mariana Lourenço, Carmen Grijota-Martínez, Soledad Bárez-López, Isabel M Miranda, Adelino Leite-Moreira, Inês Falcão-Pires, João Sérgio Neves
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引用次数: 0

Abstract

Background and aims: Metabolic dysfunction associated steatotic liver disease (MASLD) is a metabolic liver disease and thyroid hormones (TH) may decrease liver fat and extra-hepatic fat content. We aimed to evaluate the effects of high and low dose triiodothyronine (T3) in liver and subcutaneous adipose tissue (sAT) in an animal model of Metabolic Syndrome (MS).

Methods and results: Four groups were evaluated: 1) ZSF1 Lean (Lean-Ctrl, n = 8); 2) ZSF1 obese (rat model of MS with MASLD, MetS, n = 13); 3) ZSF1 obese supplemented with high-dose of T3 (MetS-hT3, n = 5); and 4) ZSF1 obese supplemented with a low-dose of T3 (MetS-lT3, n = 8). Treatment with both doses of T3 decreased body weight, liver weight and perirenal fat. High-dose T3 treatment normalized the increased expression of COL3A1 in MetS group. Histologically, lipid hepatic burden in treated groups was significantly reduced. Adipocytes and adipocytes' fibrosis areas were significantly reduced by the treatment with T3. MetS-hT3 had an increased risk of arrhythmias and sudden death.

Conclusion: Treatment with T3 improves steatosis and fibrosis at the liver and sAT in animals with MS. High doses of T3 may not be safe due to the risk of cardiac events. Our results support new therapeutic strategies for MASLD focused on the modulation of TH.

代谢综合征动物模型中三碘甲状腺原氨酸治疗对肝脏和皮下脂肪组织影响的评价。
背景和目的:代谢功能障碍相关脂肪变性肝病(MASLD)是一种代谢性肝病,甲状腺激素(TH)可降低肝脏脂肪和肝外脂肪含量。我们旨在评估高剂量和低剂量三碘甲状腺原氨酸(T3)对代谢综合征(MS)动物模型肝脏和皮下脂肪组织(sAT)的影响。方法与结果:评价四组:1)ZSF1 Lean (Lean- ctrl, n = 8);2) ZSF1肥胖(MS合并MASLD、MetS大鼠模型,n = 13);3) ZSF1肥胖患者加高剂量T3 (MetS-hT3, n = 5);4) ZSF1肥胖组补充低剂量T3 (MetS-lT3, n = 8)。两种剂量的T3治疗均能降低体重、肝脏重量和肾周脂肪。高剂量T3治疗可使met组COL3A1表达正常化。组织学上,治疗组肝脂质负荷明显减轻。T3治疗后脂肪细胞和脂肪细胞纤维化面积明显减少。met - ht3有心律失常和猝死的风险增加。结论:T3治疗可改善多发性硬化症动物肝脏和sAT的脂肪变性和纤维化,高剂量T3可能不安全,因为有心脏事件的风险。我们的研究结果支持以TH调节为重点的MASLD新治疗策略。
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来源期刊
Obesity research & clinical practice
Obesity research & clinical practice 医学-内分泌学与代谢
CiteScore
7.10
自引率
0.00%
发文量
80
审稿时长
49 days
期刊介绍: The aim of Obesity Research & Clinical Practice (ORCP) is to publish high quality clinical and basic research relating to the epidemiology, mechanism, complications and treatment of obesity and the complication of obesity. Studies relating to the Asia Oceania region are particularly welcome, given the increasing burden of obesity in Asia Pacific, compounded by specific regional population-based and genetic issues, and the devastating personal and economic consequences. The journal aims to expose health care practitioners, clinical researchers, basic scientists, epidemiologists, and public health officials in the region to all areas of obesity research and practice. In addition to original research the ORCP publishes reviews, patient reports, short communications, and letters to the editor (including comments on published papers). The proceedings and abstracts of the Annual Meeting of the Asia Oceania Association for the Study of Obesity is published as a supplement each year.
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