Effect of Compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma Extract on Pathological Changes of Myocardium in Rats after Myocardial Infarction
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Effect of Compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma Extract on Pathological Changes of Myocardium in Rats after Myocardial Infarction
Chinese Journal of Experimental Traditional Medical FormulaeVol. 19, Issue 8, Pages: 175-179(2013)
YANG Lei, MAO Bing-yu, XU Guo-chang, et al. Effect of Compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma Extract on Pathological Changes of Myocardium in Rats after Myocardial Infarction[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(8): 175-179.
DOI:
YANG Lei, MAO Bing-yu, XU Guo-chang, et al. Effect of Compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma Extract on Pathological Changes of Myocardium in Rats after Myocardial Infarction[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(8): 175-179. DOI: 10.11653/syfj2013080175.
Effect of Compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma Extract on Pathological Changes of Myocardium in Rats after Myocardial Infarction
Objective: To study the effect of compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma extract on pathological changes of myocardium in rats after myocardial infarction (MI). Method: Left coronary artery of Sprague-Dawley rats were ligated to make MI models. The rats were randomly subjected to MI model group
astragalus group
Salviae Miltiorrhizae Radix et Rhizoma group
compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma and sham-operated group
each group consisted of 8 rats. All the treatment groups were orally given 20 mg·kg-1 ·d-1 drug extract
and the MI group and sham-operated group were fed 0.9% sodium chloride 20 mL·kg-1 ·d-1. 8 weeks later
the rats were sacrificed
the hemodynamic changes in rats were determined
and the segmental heart samples were collected for hematoxylin and eosin staining
masson staining and histological evaluation on expression of protein kinase D1(PKD1). Result: Compared with the MI group
the left ventricular systolic pressure(LVSP) and maximal decrease and increase rate of pressure in left ventricle of Astragali Radix group
Salviae Miltiorrhizae Radix et Rhizoma group
compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma or sham-operated group increased significantly (P<0.01)
while the left ventricular end diastolic pressure(LVEDP) decreased significantly (P<0.01). There were serious myocardial necrosis
increased fibroblasts
accompanied by inflammatory cell infiltration in the rat of MI group
and slightly fuzzy cell morphology
nuclear hypertrophy
mild proliferation of fibroblasts
inflammatory cells decreasing in the Astragali Radix or Salviae Miltiorrhizae Radix et Rhizoma group
while clearer cell morphology
rare fibroblasts and inflammatory cells in the compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma group
according to the HE staining analysis. The masson staining results showed that the MI group consisted of more myocardial collagen tissue
yet each treatment group consist of mainly red myocardial tissue
intermingled collagen tissue. The PKD1 protein expression in the cytoplasm of myocardial tissue of the MI group increased significantly (P<0.01)
compared to all the treatment group
despite of decreasing obviously
but still visible in the Astragali Radix or Salviae Miltiorrhizae Radix et Rhizoma group. And the PKD1 protein expression in the compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma group declined significantly compared to the Astragali Radix or Salviae Miltiorrhizae Radix et Rhizoma group(P<0.05). Conclusion: Our study reveals that the compatibility of Astragali Radix and Salviae Miltiorrhizae Radix et Rhizoma can significantly ameliorate the abnormal hemorheological indicators and pathologic lesions after myocardial infarction
which may be related to the expression regulation of PKD1 protein in myocardial tissue.
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