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Toward Gene Therapy of Hypertension: Experimental Study on Hypertensive ISIAH Rats

机译:朝着高血压的基因治疗:高血压患者大鼠的实验研究

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TiO2-based nanocomposites were prepared to deliver oligonucleotides into cells. The nanocomposites were designed by the immobilization of polylysine-containing oligonucleotides on TiO2-nanoparticles (TiO2 center dot PL-DNA). We showed for the first time the possibility of using the proposed nanocomposites for treatment of hypertensive disease by introducing them into hypertensive ISIAH rats developed as a model of stress-sensitive arterial hypertension. The mRNA of the gene encoding angiotensin I-converting enzyme (ACE1) involved in the synthesis of angiotensin II was chosen as a target. Administration (intraperitoneal injection and inhalation) of the nanocomposite showed a significant (by 20-30 mm Hg) decrease in systolic blood pressure when the nanocomposite contained the ACE1 gene-targeted oligonucleotide. When using the oligonucleotide with a random sequence, no effect was observed. Further development and improvement of the inhalation nanocomposite drug delivery to systemic hypertensive disease treatment promises new possibilities for clinical practice.
机译:制备基于TiO 2的纳米复合材料以将寡核苷酸递送到细胞中。通过固定在TiO 2 - 纳米颗粒(TiO2中心点PL-DNA)上的含有聚赖氨酸寡核苷酸的固定来设计纳米复合材料。我们首次表明了使用所提出的纳米复合材料来治疗高血压疾病的可能性,通过将其引入高血压的ISIAH大鼠作为一种应激敏感动脉高血压模型。编码编码参与血管紧张素II合成的血管紧张素I-转换酶(ACE1)的基因的mRNA被选择为靶标。当纳米复合材料含有ACE1基因靶向寡核苷酸时,纳米复合材料的给药(腹膜内注射和吸入)显示出显着的(通过20-30mm Hg)的收缩压减少。当用随机序列使用寡核苷酸时,没有观察到效果。进一步的发展和改善吸入纳米复合药物给全身高血压疾病治疗的进一步发挥作用,对临床实践产生了新的可能性。

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