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Adipocytes do not significantly contribute to plasma angiotensinogen

机译:脂肪细胞对血浆血管紧张素原没有明显贡献

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摘要

Recently, it has been reported that 25% of plasma angiotensinogen (Agt) is derived from fat. Meanwhile, liver-specific Agt knockout (KO) mice have markedly low plasma Agt, which may be due to reduced fat mass. To study the contribution of the fat to plasma Agt, we tested whether increasing fat mass can elevate plasma Agt and blood pressure in liver-Agt KO mice. Epididymal fat mass in liver-Agt KO mice fed a high-fat diet (HFD) was 4.1-fold larger than that in liver-Agt KO mice on a normal-fat diet (NFD). The liver-Agt KO mice on NFD were hypotensive with low levels of plasma Agt (on average, 0.11 vs 2.38 μg/ml). HFD slightly increased plasma Agt (0.17 μg/ml) without increase in blood pressure. To further increase fat mass, liver-Agt KO mice were fed HFD and simultaneously supplemented with low-dose angiotensin II and compared with control mice. Fat mass was comparable between the two groups. However, liver-Agt KO mice had uniformly low plasma Agt (0.09 vs 2.07 μg/ml) and systolic blood pressure (78±12 vs 111±6 mm Hg). In conclusion, adipocyte-derived Agt has essentially no contribution to the plasma concentration and no impact on blood pressure compared to liver-derived Agt.
机译:最近,据报道血浆血管紧张素原(Agt)的25%来自脂肪。同时,肝脏特异性Agt基因敲除(KO)小鼠血浆Agt明显较低,这可能是由于脂肪量减少所致。为了研究脂肪对血浆Agt的贡献,我们测试了增加脂肪量是否可以提高肝Agt KO小鼠的血浆Agt和血压。高脂饮食(HFD)喂养的肝Agt KO小鼠的附睾脂肪量是正常脂肪饮食(NFD)喂养的肝Agt KO小鼠的附睾脂肪量的4.1倍。 NFD上的Agt肝小鼠降压,血浆Agt低(平均0.11对2.38μg/ ml)。 HFD会稍微增加血浆Agt(0.17μg/ ml),而不会导致血压升高。为了进一步增加脂肪量,给肝-Agt KO小鼠喂饲HFD,同时补充低剂量的血管紧张素II,并与对照小鼠进行比较。两组之间的脂肪量相当。但是,肝Agt KO小鼠的血浆Agt(0.09 vs.2.07μg/ ml)和收缩压(78±12 vs 111±6 mm Hg)一致较低。总之,与肝脏来源的Agt相比,脂肪细胞来源的Agt对血浆浓度基本没有贡献,对血压也没有影响。

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