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Insulin: too much of a good thing is bad

机译:胰岛素:太多好事是坏事

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Insulin shares a limited physiological concentration range with other endocrine hormones. Not only too low, but also too high systemic insulin levels are detrimental for body functions. The physiological function and clinical relevance of insulin are usually seen in association with its role in maintaining glucose homeostasis. However, insulin is an anabolic hormone which stimulates a large number of cellular responses. Not only too low, but also excess insulin concentrations are detrimental to the physiological balance. Although the glucoregulatory activity of insulin is mitigated during hyperinsulinemia by dampening the efficiency of insulin signaling (“insulin resistance”), this is not the case for most other hormonal actions of insulin, including the promotion of protein synthesis, de novo lipogenesis, and cell proliferation; the inhibition of lipolysis, of autophagy-dependent cellular turnover, and of nuclear factor E2-related factor-2 (Nrf2)-dependent antioxidative; and other defense mechanisms. Hence, there is no general insulin resistance but selective impairment of insulin signaling which causes less glucose uptake from the blood and reduced activation of endothelial NO synthase (eNOS). Because of the largely unrestricted insulin signaling, hyperinsulinemia increases the risk of obesity, type 2 diabetes, and cardiovascular disease and decreases health span and life expectancy. In epidemiological studies, high-dose insulin therapy is associated with an increased risk of cardiovascular disease. Randomized controlled trials of insulin treatment did not observe any effect on disease risk, but these trials only studied low insulin doses up to 40?IU/day. Proof for a causal link between elevated insulin levels and cardiovascular disease risk comes from Mendelian randomization studies comparing individuals with genetically controlled low or high insulin production. The detrimental actions of prolonged high insulin concentrations, seen also in cell culture, argue in favor of?a lifestyle?that?limits circadian insulin levels. The health risks associated with hyperinsulinemia may have implications for treatment regimens used in type 2 diabetes.
机译:胰岛素与其他内分泌激素共享有限的生理浓度范围。不仅太低,而且过高的全身胰岛素水平对身体功能有害。胰岛素的生理功能和临床相关性通常与其在维持葡萄糖稳态中的作用相关。然而,胰岛素是一种代谢激素,其刺激大量细胞反应。不仅太低,而且过多的胰岛素浓度对生理平衡有害。虽然通过抑制胰岛素信号传导的效率(“胰岛素抵抗”)在高胰岛素血症期间减轻胰岛素的葡萄糖活性,但对于胰岛素的大多数其他荷尔蒙行为,尤其是胰岛素的含量,包括促进蛋白质合成,DE Novo脂肪生成和细胞的情况并非如此。增殖;抑制脂解,依赖性细胞周转和核因子E2相关因子-2(NRF2) - 依赖性抗氧化;和其他防御机制。因此,没有一般性胰岛素抵抗,而是对胰岛素信号传导的选择性损害,这导致血液的血糖摄取并降低内皮未合成酶(ENOS)的活化。由于基本上不受限制的胰岛素信号传导,高胰岛素血症会增加肥胖,2型糖尿病和心血管疾病的风险,并降低健康跨度和预期寿命。在流行病学研究中,高剂量胰岛素治疗与心血管疾病的风险增加有关。胰岛素治疗的随机对照试验并没有观察到任何对疾病风险的影响,但这些试验仅研究了低至40℃/天的低胰岛素剂量。胰岛素水平升高和心血管疾病风险之间的因果关系的证据来自孟德尔随机化研究,比较遗传控制的低或高胰岛素生产的个体。延长高胰岛素浓度的不利作用,也可以在细胞培养中争辩,有利于?一种生活方式?这?限制昼夜胰岛素水平。与高胰岛素血症相关的健康风险可能对2型糖尿病中使用的治疗方案有影响。

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