1. 青海省中医院科研所,青海,西宁,810000
2. 上海中医药大学交叉科学研究院,上海,201203
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贾守宁, 陈文娟, 李欣, 等. 红景天苷对高原红细胞增多症大鼠促红细胞生成素及骨髓病理学影响的研究[J]. 上海中医药杂志, 2020,54(7):94-98.
JIA Shouning, CHEN Wenjuan, LI Xin, et al. Effects of salidroside on erythropoietin and bone marrow pathology in rats with high altitude polycythemia[J]. Shanghai Journal of Traditional Chinese Medicine, 2020,54(7):94-98.
贾守宁, 陈文娟, 李欣, 等. 红景天苷对高原红细胞增多症大鼠促红细胞生成素及骨髓病理学影响的研究[J]. 上海中医药杂志, 2020,54(7):94-98. DOI: 10.16305/j.1007-1334.2020.07.014.
JIA Shouning, CHEN Wenjuan, LI Xin, et al. Effects of salidroside on erythropoietin and bone marrow pathology in rats with high altitude polycythemia[J]. Shanghai Journal of Traditional Chinese Medicine, 2020,54(7):94-98. DOI: 10.16305/j.1007-1334.2020.07.014.
目的:观察红景天苷对高原红细胞增多症(HAPC)大鼠促红细胞生成素(EPO)及骨髓病理学的影响。 方法:将40只SPF级Wistar大鼠随机分为正常对照组、模型组及治疗高、中、低剂量组,每组8只。除正常对照组外,其余4组按照文献方法复制HAPC大鼠模型;治疗高、中、低剂量组分别灌胃给予200 mg/kg、100 mg/kg和50 mg/kg剂量的红景天苷,模型组和正常对照组分别灌胃给予等体积的0.9%NaCl溶液,各组均干预40 d。采用酶联免疫吸附法测定血清中EPO的水平,Western blot法测定肾脏中EPO的水平;制作骨髓病理涂片,HE染色后,显微镜观察骨髓细胞形态及分类情况,并进行细胞学计数。 结果:①与模型组相比,治疗高、中、低剂量组大鼠的肾脏及血清中EPO水平均有显著下调,差异有统计学意义(P<0.01);尤其是血清中EPO水平的下调呈显著的剂量依赖性。②治疗低剂量组大鼠骨髓象红细胞系增生活跃,主要是晚幼红细胞增生活跃,与模型组大鼠骨髓象比较没有明显的形态学变化,各指标差异无统计学意义(P>0.05)。③治疗中剂量组大鼠骨髓象虽然有红细胞系增生,但晚幼红细胞和成熟红细胞增生并不明显,且成熟红细胞形态正常,粒细胞/有核红细胞比值与模型组相比差异有统计学意义(P<0.05)。④治疗高剂量组骨髓象粒细胞系和红细胞系比例趋于正常,与模型组骨髓象比较,晚幼红细胞增生并不活跃,成熟红细胞形态正常,指标中有核红细胞比例、粒细胞比例、粒细胞/有核红细胞比值差异有统计学意义(P<0.01)。 结论:红景天苷可调控HAPC大鼠EPO的过度表达,并可改善骨髓象红细胞系的过度代偿性增生。
Objective:To observe the effect of salidroside on erythropoietin (EPO) level and bone marrow pathology in rats with high altitude polycythemia (HAPC) after intervention, and to explore the mechanism of salidroside in preventing and treating HAPC.MethodsForty SPF Wistar rats were randomly divided into normal control group, model group and high, middle and low dose groups with 8 rats in each group. Except the normal control group, the other 4 groups duplicated HAPC rat models according to the methods from the literature. Salidroside was administered to the high, middle and low dose groups by gavage at doses of 200 mg/kg, 100 mg/kg and 50 mg/kg respectively, while the equal volume of 0.9% NaCl solution was administered to the model group and the normal control group by gavage respectively. All groups were intervened for 40 days.The levels of EPO in serum and kidney were determined by ELISA and Western blot respectively. Pathological smears of bone marrow were made. After HE staining, the morphology, classification and cytological counting of bone marrow cells were observed under microscope. Results:①Compared with the model group, EPO levels in kidney and serum of rats in the high, middle and low dose groups were significantly reduced, and the difference was statistically significant (P<0.01). In particular, the down-regulation of EPO level in serum was significantly dose-dependent. ②The bone marrow erythron of rats in the low dose group proliferated actively, mainly the orthochromatic erythroblasts; Compared with the bone marrow erythron of rats in the model group, no obvious morphological change was found in the low dose group, and there was no significant difference in each index (P>0.05).③Although there was erythroid hyperplasia in the bone marrow of rats in the middle dose group, the hyperplasia of orthochromatic erythroblasts and mature erythrocytes was not significant, the morphology of mature erythrocytes was normal, and the ratio of granulocyte to nucleated erythrocyte was significantly different from that in the model group (P<0.05).④The proportion of bone marrow granulocyte series and erythron in the high dose group tended to be normal.Compared with the model group, the proliferation of orthochromatic erythroblasts was not active, the morphology of mature erythrocyte was normal, and the proportion of nucleated erythrocyte, the proportion of granulocyte and the ratio of granulocyte to nucleated erythrocyte in the test were significantly different (P<0.01). Conclusion:Salidroside can regulate the overexpression of EPO in HAPC rats and improve the excessive compensatory proliferation of bone marrow erythron.
高原红细胞增多症大鼠红景天苷促红细胞生成素骨髓病理
high altitude polycythemiaratssalidrosideerythropoietinbone marrow pathology
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