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A glucose-stimulated BOLD fMRI study of hypothalamic dysfunction in mice fed a high-fat and high-sucrose diet.高脂肪高蔗糖饮食喂养的小鼠下丘脑功能障碍的葡萄糖刺激 BOLD fMRI 研究。
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2
Magnetic resonance assessment of the cerebral alterations associated with obesity development.磁共振评估与肥胖发展相关的大脑改变。
J Cereb Blood Flow Metab. 2020 Nov;40(11):2135-2151. doi: 10.1177/0271678X20941263. Epub 2020 Jul 23.
3
The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research.《ARRIVE指南2.0:动物研究报告的更新指南》
J Cereb Blood Flow Metab. 2020 Sep;40(9):1769-1777. doi: 10.1177/0271678X20943823. Epub 2020 Jul 14.
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Pediatr Gastroenterol Hepatol Nutr. 2020 May;23(3):189-230. doi: 10.5223/pghn.2020.23.3.189. Epub 2020 May 8.
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Impaired endothelium-mediated cerebrovascular reactivity promotes anxiety and respiration disorders in mice.内皮细胞介导的脑血管反应性受损可促进小鼠焦虑和呼吸障碍。
Proc Natl Acad Sci U S A. 2020 Jan 21;117(3):1753-1761. doi: 10.1073/pnas.1907467117. Epub 2020 Jan 2.
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Telmisartan prevents development of obesity and normalizes hypothalamic lipid droplets.替米沙坦可预防肥胖的发生,并使下丘脑脂滴正常化。
J Endocrinol. 2020 Jan 1;244(1):95-110. doi: 10.1530/JOE-19-0319.
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Monosynaptic Hippocampal-Prefrontal Projections Contribute to Spatial Memory Consolidation in Mice.单突触海马体-前额叶投射有助于小鼠的空间记忆巩固。
J Neurosci. 2019 Aug 28;39(35):6978-6991. doi: 10.1523/JNEUROSCI.2158-18.2019. Epub 2019 Jul 8.
8
The antiobese effect of AT1 receptor blockade is augmented in mice lacking Mas.Mas 缺失的小鼠中 AT1 受体阻断的抗肥胖作用增强。
Naunyn Schmiedebergs Arch Pharmacol. 2019 Jul;392(7):865-877. doi: 10.1007/s00210-019-01643-0. Epub 2019 Mar 13.
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The obesity transition: stages of the global epidemic.肥胖流行的转变:全球流行阶段。
Lancet Diabetes Endocrinol. 2019 Mar;7(3):231-240. doi: 10.1016/S2213-8587(19)30026-9. Epub 2019 Jan 28.
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Obesity-Induced Cellular Senescence Drives Anxiety and Impairs Neurogenesis.肥胖诱导的细胞衰老引发焦虑并损害神经发生。
Cell Metab. 2019 May 7;29(5):1061-1077.e8. doi: 10.1016/j.cmet.2018.12.008. Epub 2019 Jan 3.

替米沙坦可预防高脂饮食引起的神经血管损伤,并降低焦虑样行为。

Telmisartan prevents high-fat diet-induced neurovascular impairments and reduces anxiety-like behavior.

机构信息

Institute of Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany.

CBBM (Centre for Brain, Behavior and Metabolism), University of Lübeck, Lübeck, Germany.

出版信息

J Cereb Blood Flow Metab. 2021 Sep;41(9):2356-2369. doi: 10.1177/0271678X211003497. Epub 2021 Mar 17.

DOI:10.1177/0271678X211003497
PMID:33730932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8393307/
Abstract

Angiotensin II receptor blockers (telmisartan) prevent rodents from diet-induced obesity and improve their metabolic status. Hyperglycemia and obesity are associated with reduced cerebral blood flow and neurovascular uncoupling which may lead to behavioral deficits. We wanted to know whether a treatment with telmisartan prevents these changes in obesity.We put young mice on high-fat diet and simultaneously treated them with telmisartan. At the end of treatment, we performed laser speckle imaging and magnetic resonance imaging to assess the effect on neurovascular coupling and cerebral blood flow. Different behavioral tests were used to investigate cognitive function.Mice developed diet-induced obesity and after 16, not 8 weeks of high-fat diet, however, the response to whisker pad stimulation was about 30% lower in obese compared to lean mice. Simultaneous telmisartan treatment increased the response again by 10% compared to obese mice. Moreover, telmisartan treatment normalized high-fat diet-induced reduction of cerebral blood flow and prevented a diet-induced anxiety-like behavior. In addition to that, telmisartan affects cellular senescence and string vessel formation in obesity.We conclude, that telmisartan protects against neurovascular unit impairments in a diet-induced obesity setting and may play a role in preventing obesity related cognitive deficits in Alzheimer's disease.

摘要

血管紧张素 II 受体阻滞剂(替米沙坦)可预防饮食诱导的肥胖,并改善其代谢状态。高血糖和肥胖与脑血流减少和神经血管解耦联有关,这可能导致行为缺陷。我们想知道替米沙坦治疗是否可以预防肥胖引起的这些变化。我们让年轻小鼠食用高脂肪饮食,并同时给予替米沙坦治疗。在治疗结束时,我们进行激光散斑成像和磁共振成像,以评估对神经血管耦合和脑血流的影响。使用不同的行为测试来研究认知功能。小鼠发展为饮食诱导的肥胖,在高脂肪饮食 16 周后,而不是 8 周后,肥胖小鼠对胡须垫刺激的反应比瘦小鼠低约 30%。替米沙坦治疗将反应再次提高了 10%,与肥胖小鼠相比。此外,替米沙坦治疗还可以纠正高脂肪饮食引起的脑血流减少,并预防焦虑样行为。此外,替米沙坦还可以影响肥胖中的细胞衰老和血管形成。我们的结论是,替米沙坦可预防饮食诱导的肥胖模型中的神经血管单元损伤,并可能在预防阿尔茨海默病相关的肥胖认知缺陷中发挥作用。