首页> 外文期刊>Chinese Jouranl of Integrative Medicine >Effects of Qindan Capsule on Blood Pressure, Endothelin, Calcitonin Gene-related Peptide and Angiotensin-II in Spontaneous Hypertensive Rats
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Effects of Qindan Capsule on Blood Pressure, Endothelin, Calcitonin Gene-related Peptide and Angiotensin-II in Spontaneous Hypertensive Rats

机译:秦丹胶囊对自发性高血压大鼠血压,内皮素,降钙素基因相关肽和血管紧张素Ⅱ的影响

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Objective: To observe the hypotensive effects of Qindan Capsule (QC) on spontaneous hypertensive rats (SHR) and its effect on the contents of endothelin (ET), calcitonin gene-related peptide (CGRP) and angiotensin-II (Ang-II) in plasma and vascular tissues, and to investigate the possible mechanism of QC in lowering blood pressure. Methods: Forty SHRs were divided into 5 groups: the high dosage QC group [QCHD, 750 mg/(kg·d)], the low dosage QC group [QCLD, 150 mg/(kg·d)], the Niuhuang Jiangya Pill group [NJP, 200 mg/(kg·d)], the Captopril group [15 mg/(kg·d)] and the model group, 8 in each group. Meanwhile, a normal control group consisting of 8 Wistar-Kyoto (WKY) rats was set up also. All the rats were administered with medicine through gastrogavage. Systolic blood pressure (SBP), level of ET, CGRP and Ang-II in plasma and Ang-II in tissues of mesenteric artery were detected in all the rats after 12 weeks of treatment. Results: The level of SBP after treatment in the QCHD group was lower than that in the model group (P < 0. 01), but with no significant difference as compared with that in the Captopril group and the NJP group (P > 0. 05). After treatment, the plasma level of ET was lower and CGRP higher than those in the model group (both P < 0. 05), and also higher than those in the NJP and Captopril group (both P < 0. 05). As for the content of Ang-II, in mesenteric arterial tissues, it was lower in the QCHD group than that in the model group (P < 0.05), but in plasma, it showed no significant difference between the two groups (P > 0.05). Conclusion: QC has a satisfactory hypotensive action on SHR rats, and its mechanism may be associated with the regulation on plasma vasoactive peptide and regional renin-angiotensin system.
机译:目的:观察秦丹胶囊(QC)对自发性高血压大鼠(SHR)的降压作用及其对内皮素(ET),降钙素基因相关肽(CGRP)和血管紧张素II(Ang-II)含量的影响。血浆和血管组织,并研究QC降低血压的可能机制。方法:将40例SHR分为5组:高剂量QC组[QCHD,750 mg /(kg·d)],低剂量QC组[QCLD,150 mg /(kg·d)],牛黄降压丸组[NJP,200mg /(kg·d)],卡托普利组[15mg /(kg·d)]和模型组,每组8个。同时,还建立了由8只Wistar-Kyoto(WKY)大鼠组成的正常对照组。所有大鼠通过胃灌胃给药。治疗12周后,在所有大鼠中检测收缩压(SBP),血浆ET,CGRP和Ang-II水平以及肠系膜动脉组织中Ang-II水平。结果:QCHD组治疗后的SBP水平低于模型组(P <0. 01),但与卡托普利组和NJP组相比无显着差异(P> 0。 05)。治疗后,血浆ET水平和CGRP均低于模型组(均P <0. 05),也高于NJP和卡托普利组(均P <0. 05)。关于Ang-II的含量,QCHD组肠系膜动脉组织低于模型组(P <0.05),而血浆中两组之间无显着性差异(P> 0.05)。 )。结论:QC对SHR大鼠具有良好的降压作用,其机制可能与调节血浆血管活性肽和区域性肾素-血管紧张素系统有关。

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