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首页> 外文期刊>Life sciences >Peptide nucleic acids specifically cause antigene effects in vivo by systemic injection.
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Peptide nucleic acids specifically cause antigene effects in vivo by systemic injection.

机译:肽核酸通过全身注射在体内特异性地引起抗原作用。

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Peptide nucleic acids (PNAs) are uncharged DNA analogs that hybridize to complementary sequences with high affinity and stability. We previously showed that PNAs, after intraperitoneal injection into rats, are effective antisense compounds in vivo. The present study was designed to test whether PNAs also have antigene effects in vivo. The renin-angiotensin system is critical in the control of blood pressure. We designed and synthesized sense (antigene) PNAs to angiotensinogen, which is the precursor protein that leads to angiotensin I and II. Spontaneously hypertensive rats received intraperitoneal injections of either 20 mg/kg sense-angiotensinogen-PNA, mismatch-angiotensinogen PNA, or saline. Only the sense-angiotensinogen PNA treatment resulted in a significant decrease in plasma angiotensin I, systolic blood pressure, and liver and brain angiotensinogen mRNA levels. Thus, these results demonstrate on the molecular, protein, and physiological levels that antigene PNAs are effective in vivo upon systemic administration.
机译:肽核酸(PNA)是不带电荷的DNA类似物,可与互补序列高亲和力和稳定性杂交。我们先前显示,腹膜内注射到大鼠体内后,PNA在体内是有效的反义化合物。本研究旨在测试PNA是否在体内也具有抗原作用。肾素-血管紧张素系统对控制血压至关重要。我们设计并合成了针对血管紧张素原的有义(抗原)PNA,血管紧张素原是导致血管紧张素I和II的前体蛋白。自发性高血压大鼠接受腹膜内注射20 mg / kg有义血管紧张素原-PNA,错配血管紧张素原PNA或盐水。只有有意识的血管紧张素原PNA治疗可导致血浆血管紧张素I,收缩压以及肝和脑血管紧张素原mRNA水平显着降低。因此,这些结果在分子,蛋白质和生理水平上证明了抗原PNA在全身给药后在体内是有效的。

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