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1.黑龙江中医药大学 中医药研究院,哈尔滨 150040;
2.黑龙江中医药大学 药物安全性评价中心,哈尔滨 150040
白宛鑫,博士,从事中药药性理论相关问题研究,Tel:0451-82193278,E-mail: 1762822831@qq.com
刘树民,教授,博士生导师,从事中药药性及中药毒性研究,Tel:0451-82193278,E-mail: keji-liu@163.com
收稿日期:2018-07-15,
网络出版日期:2018-11-21,
纸质出版日期:2019-03-05
移动端阅览
白宛鑫, 赵良友, 张娜, 等. 生淫羊藿与炙淫羊藿对肾阳虚证水肿模型大鼠的影响[J]. 中国实验方剂学杂志, 2019,25(5):85-91.
Wan-xin BAI, Liang-you ZHAO, Na ZHANG, et al. Effect of Crude Epimedii Folium and Processed Epimedii Folium on Kidney Yang Deficiency Edema Model Rats[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(5): 85-91.
白宛鑫, 赵良友, 张娜, 等. 生淫羊藿与炙淫羊藿对肾阳虚证水肿模型大鼠的影响[J]. 中国实验方剂学杂志, 2019,25(5):85-91. DOI: 10.13422/j.cnki.syfjx.20190501.
Wan-xin BAI, Liang-you ZHAO, Na ZHANG, et al. Effect of Crude Epimedii Folium and Processed Epimedii Folium on Kidney Yang Deficiency Edema Model Rats[J]. Chinese journal of experimental traditional medical formulae, 2019, 25(5): 85-91. DOI: 10.13422/j.cnki.syfjx.20190501.
目的:
2
研究生品与炮制后的淫羊藿对肾阳虚水肿模型大鼠的作用,为阐明炮制前后淫羊藿治疗肾阳虚水肿的作用机制。
方法:
2
用氢化可的松联合盐酸多柔比星复制肾阳虚水肿大鼠模型,即造模第1,8天分别尾静脉注射盐酸多柔比星(3.5mg·kg
-1
),与此同时,连续14d腹腔注射强化可的松注射液(3.75mg·kg
-1
·d
-1
)进行造模,造模结束后将造模成功的大鼠分为模型组,生淫羊藿组(204.86mg·kg
-1
),炙淫羊藿组(204.86mg·kg
-1
),同时设立正常组,各组大鼠分别给予相应药物(10mL·kg
-1
),正常组和模型组给予同体积蒸馏水,连续灌胃14d。给药结束后,大鼠代谢笼法测24h尿量,采用紫外分光光度法测定尿液中尿蛋白的含量;血清中指标的测定,采用全自动生化分析仪测血浆白蛋白(ALB),血清总蛋白(TP),血清肌酐(SCr),血清尿素氮(BUN)含量;采用酶联免疫测定(ELISA)检测环磷酸腺苷(cAMP),环磷酸鸟苷(cGMP),三碘甲状腺原氨酸(T
3
),甲状腺素(T
4
),雌二醇(E
2
),睾酮(T)指标含量,取肾脏适量做苏木素-伊红(HE)染色病理切片。
结果:
2
与正常组比较,模型组大鼠从外观指标,生化指标,病理切片指标上均证明模型组大鼠处于肾阳虚水肿状态(
P
<
0.05,
P
<
0.01);与模型组比较,生淫羊藿给药组与炙淫羊藿给药组对肾阳虚水肿的外观指标与病理切片指标均有回调作用,且在生化指标上,生、炙淫羊藿给药组均能回调尿量,尿蛋白,SCr
BUN
cAMP/cGMP
E
2
,T指标(
P
<
0.05,
P
<
0.01),但是回调强度有所不同。生淫羊藿给药组极显著性回调尿量,尿蛋白,SCr
BUN(
P
<
0.01);炙淫羊藿给药组极显著性回调cAMP/cGMP
E
2
,T(
P
<
0.01)。此外,生淫羊藿给药组还可以回调ALB
TP(
P
<
0.05,
P
<
0.01),而炙淫羊藿给药组对这2个指标没有回调作用,炙淫羊藿给药组可以回调T
3
,T
4
,肛温(
P
<
0.05,
P
<
0.01),而生淫羊藿给药组对这2个指标没有回调作用。
结论:
2
生淫羊藿与炙淫羊藿给药组均可以治疗肾阳虚水肿,机制可能与改善阿霉素所致的肾小球足细胞损伤有关。生淫羊藿与炙淫羊藿治疗肾阳虚水肿侧重点有所不同,生淫羊藿性寒,更侧重于加强肾阳虚水肿大鼠的肾脏排泄功能来治疗肾阳虚水肿。炙淫羊藿经羊油炮制后产生了淫羊藿苷等物质,药性由寒转温,偏重改善肾阳虚水肿大鼠肾阳虚状态来治疗肾阳虚水肿。
Objective:
2
To compare the effects between crude and processed Epimedii Folium on the rats of kidney-Yang deficiency and edema
in order to discuss the mechanism.
Method:
2
The rat model of kidney-Yang edema was duplicated with hydrocortisone and doxorubicin hydrochloride. At day 1 and day 8 of modeling
the rats were injected with doxorubicin hydrochloride (3.5mg·kg
-1
) via tail vein
while being intraperitoneally injected with hydrocortisone (3.75mg·kg
-1
·d
-1
) for 15days.After modeling
the rats were divided into model group
crude Epimedii Folium group(204.86mg·kg
-1
)and processed Epimedii Folium group(204.86mg·kg
-1
)
and a normal control group was set up additionally.Rats in each treatment group were given the corresponding drugs
and those in normal and model groups were given the same volume of normal saline by gavage for continuous 14days.At the end of the administration
24h urine was measured by rat metabolic cage method; 24h urinary protein was detected by ultraviolet spectrophotometry; the content of plasma albumin (ALB) and total serum protein (TP) were measured by an automatic biochemical analyzer; and the content of adenosine monophosphate was measured by enzyme-linked immunosorbent assay(ELISA). Cyclic adenosine monophosphate (cAMP)
cyclic guanosine monophosphate (cGMP)
triiodothyronine (T
3
)
thyroxine (T
4
)
serum creatinine (SCr)
serum urea(BUN)
estradiol (E
2
)
testosterone (T) indicator content were determined by enzyme-linked immunosorbent assay(ELISA). Kidney tissues were collected to make pathological section by htoxylin eosin(HE) staining.
Result:
2
Compared with the normal group
all the indicators of appearance
biochemistry and pathological section in the model group indicated kidney Yang deficiency edema in the rats (
P
<
0.05
P
<
0.01). Compared with the model group
both crude Epimedii Folium group and processed Epimedii Folium group showed a regulatory effect on indicators of appearance and pathological section kidney Yang deficiency edema; and in biochemical indicators
both crude Epimedii Folium group and processed Epimedii Folium group can regulate urine
urine protein
SCr
BUN
cAMP/cGMP
E
2
T indicators to varying degrees(
P
<
0.05
P
<
0.01). Crude Epimedii Folium group showed a significantly regulatory effect on urine
urine protein
SCr
BUN (
P
<
0.01); whereas processed Epimedii Folium group showed a significantly regulatory effect on cAMP/cGMP
E
2
T (
P
<
0.01). In addition
crude Epimedii Folium group can also regulate ALB
TP (
P
<
0.05
P
<
0.01)
while processed Epimedii Folium group had no regulatory effect on these two indicators; however
processed Epimedii Folium group could regulate T
3
T
4
and anal temperature (
P
<
0.05
P
<
0.01)
while crude Epimedii Folium group had no regulatory effect on these two indicators.
Conclusion:
2
Both crude Epimedii Folium group and processed Epimedii Folium group have certain effect in treating kidney Yang deficiency edema
and the possible mechanism is to alleviate glomerular podocyte injury induced by doxorubicin. Their emphasis in the treatment of kidney Yang deficiency edema is different. Crude Epimedii Folium has a cold property
and can treat kidney Yang deficiency edema by strengthening renal excretion function of rats with kidney Yang deficiency edema. Processed Epimedii Folium is processed with sheep oil to produce icariin and other substances
and its property changed from cold to warm
with a focus on alleviating the kidney Yang deficiency status of rats with kidney Yang deficiency edema.
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