Effect of miRNA-483-3p in regulating and controlling blood pressure, heart and blood vessels of spontaneously hypertensive rats

A spontaneous, high blood pressure technology, applied to cardiovascular system diseases, medical preparations containing active ingredients, pharmaceutical formulas, etc.

Pending Publication Date: 2020-08-07
FUJIAN UNIV OF TRADITIONAL CHINESE MEDICINE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is no report on the role of miRNA-483-3p in regulating blood pressure, heart and blood vessels in spontaneously hypertensive rats

Method used

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  • Effect of miRNA-483-3p in regulating and controlling blood pressure, heart and blood vessels of spontaneously hypertensive rats
  • Effect of miRNA-483-3p in regulating and controlling blood pressure, heart and blood vessels of spontaneously hypertensive rats
  • Effect of miRNA-483-3p in regulating and controlling blood pressure, heart and blood vessels of spontaneously hypertensive rats

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Example 1 Effect of miR-483-3p on blood pressure in spontaneously hypertensive (Spontaneously Hypertensive Rats, SHR) rats

[0031] 1 group of rats

[0032] 32 healthy SPF-grade Wistar and SHR male rats, weighing 200±20g, were raised in an SPF-grade laboratory, free to move, eat and drink freely, ventilated, with sufficient light, and the room temperature was controlled at (25±1)°C, relatively The humidity was 70%-80%, and the experiment was carried out after 7 days of adaptive feeding. SHR rats were randomly divided into 3 groups according to the basic blood pressure method, namely SHR group, SHR+NC group, SHR+mir-483-3p group, 8 rats in each group.

[0033] Tail vein injection method

[0034] (1) The tail vein injection of HBAAV2 / 9-GFP NC in the SHR+NC group interfered with the control empty expression vector (titer: 1.6*10 12 TU / ml, 162.5ul), the SHR+miR-483-3p group was injected with HBAAV2 / 9-rno-mir-483-3p-sponge-GFP (titer: 1.3*10 12 TU / ml, 200 µL) adenovirus ...

Embodiment 2

[0037] Example 2 The effect of miR-483-3p on the heart structure and function of SHR rats

[0038] Animal grouping and administration methods are the same as in Example 1.

[0039] At the end of the experiment, EF, FS and HWI were detected by small animal ultrasound, and the results are shown in the appendix Figure 4-6 .

[0040] attached by Figure 4-6 It is known that rat heart function was measured by echocardiography: Compared with rats in wistar group, EF and FS of rats in NC and SHR groups were significantly decreased (p<0.05), compared with rats in NC and SHR groups, miR-483- The EF and FS of the rats in the 3p group were significantly increased (p<0.05). In addition, compared with wistar rats, the HWI of the rats in the SHR and NC groups was significantly increased (p<0.05), and compared with the rats in the SHR and NC groups, the HWI of the rats in the miR-483-3p group was decreased (p<0.05).

Embodiment 3

[0041] Example 3 The effect of miR-483-3p on the structure of abdominal aorta in SHR rats

[0042] Animal grouping and administration methods are the same as in Example 1.

[0043] After the experiment, the rats were anesthetized with isoflurane and sacrificed, the heart was dissected and weighed, and the heart mass index (ratio of heart weight / tibia length (mg / mm)) was calculated. The apex of the heart tissue was removed, frozen in liquid nitrogen, and stored at -80°C until subsequent experiments. The rest were fixed with 4% paraformaldehyde for pathological analysis, embedded in paraffin for routine histological processing, prepared 4 μm slices, and observed inflammatory cell infiltration and myocardial necrosis by HE staining. Figure 7-10 ; Masson staining was used to analyze the degree of myocardial fibrosis, the results are shown in the appendix Figure 11-14 .

[0044] attached by Figure 7-10It is known that rat abdominal aorta showed HE staining: Wistar group arte...

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Abstract

The invention relates to an effect of miRNA-483-3p in regulating and controlling blood pressure, heart and blood vessels of spontaneously hypertensive rats. The systolic pressure, diastolic pressure and average arterial pressure of spontaneously hypertensive rats can be kept within an initial range and are not continuously increased any more. The cardiac ejection fraction and the left ventricularminor axis shortening rate can be obviously increased, and the cardiac weight index is reduced, so that the cardiac structure and function are obviously improved. The aorta abdominalis collagen fiberscan be reduced, the intima is obviously thinned, the lumen is widened, and endothelial cells are arranged in order, so that the aorta abdominalis structure, thickness and intima integrity are improved to different extents. Therefore, the miRNA-483-3p disclosed by the invention can be used as a new target for treating hypertension.

Description

technical field [0001] The invention relates to the application of microRNA (miRNA) in regulating hypertension, in particular to the role of miRNA-483-3p in regulating blood pressure, heart and blood vessels in spontaneously hypertensive rats. Background technique [0002] Hypertension is the most common cardiovascular disease in my country, which can lead to a variety of serious complications, such as chronic heart failure, chronic renal failure, and stroke. The etiology and pathogenesis of hypertension are complex, involving multiple effector organs and target organs. Currently, there are six categories of antihypertensive drugs recommended for clinical use: diuretics, calcium antagonists, β-receptor antagonists, α1-receptor antagonists, angiotensin converting enzyme inhibitors, and angiotensin II receptor antagonists. These drugs mainly control blood pressure and prevent complications, but cannot achieve a radical effect. [0003] The unclear etiology and pathogenesis o...

Claims

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Application Information

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IPC IPC(8): A61K31/7105A61P9/12A61P9/00A61P9/14
CPCA61K31/7105A61P9/12A61P9/00A61P9/14
Inventor褚剑锋彭军沈阿灵曾建伟杨美玲彭美中周雪玲
OwnerFUJIAN UNIV OF TRADITIONAL CHINESE MEDICINE