1.730000 兰州,甘肃中医药大学药学院
2.730050 兰州,中国人民解放军联勤保障部队第九四○医院药剂科
3.710061 西安,西安交通大学医学院第一附属医院药学部
Received:16 December 2022,
Revised:2023-02-11,
Published:30 July 2023
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Hongqiang TAN, Jie ZHANG, Pengpeng ZHANG, et al. Protective effect of n-butanol extract of
Hongqiang TAN, Jie ZHANG, Pengpeng ZHANG, et al. Protective effect of n-butanol extract of
目的
2
研究矮垂头菊正丁醇提取物(n-butanol extract of
Cremanthodium humile
,BECH)对低压低氧小鼠心肌损伤的保护作用。
方法
2
取清洁级BALB/c雄性小鼠50只分为(
n
=10):缺氧模型组、乙酰唑胺组,BECH低(125 mg/kg)、中(250 mg/kg)、高剂量(500 mg/kg)组进行常压密闭缺氧实验确定最佳给药剂量。30只小鼠分为(
n
=10):急性减压组、乙酰唑胺组、BECH给药组进行减压缺氧耐受实验确定最佳给药剂量的存活率。52只小鼠分为(
n
=13):正常对照组、低压低氧组、乙酰唑胺组和BECH给药组,连续灌胃5 d,第5天给药后,正常对照组置于当地海拔,其余小鼠置于低压低氧动物实验舱中。模拟海拔高度8 000 m暴露24 h,摘眼球取血后随即处死,HE染色观察小鼠心肌组织病理变化;测定血清中肌酸激酶(creatine kinase,CK)、谷草转氨酶(aspartate aminotransferase,AST)、心肌肌钙蛋白I(cardiac troponin I,c-TnI)活性;测定心肌组织中活性氧(reactive oxygen species,ROS)、过氧化氢酶(catalase,CAT)、丙二醛(malondialdehyde,MDA)、超氧化物歧化酶(superoxide dismutase,SOD)、乳酸(lactic acid,LD)、乳酸脱氢酶(lactate dehydrogenase,LDH)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)和总抗氧化能力(total antioxidant capacity,T-AOC)含量和水平;蛋白印迹法检测心肌组织中Nrf-2、HO-1、Bax、Bcl-2、cleaved Caspase-3蛋白的表达水平。
结果
2
与缺氧模型组相比,BECH可以显著延长常压密闭缺氧小鼠的存活时间,且以高剂量组效果较好;与急性减压组相比,BECH给药组能够显著降低急性减压小鼠的死亡率。与正常对照组相比,低压低氧组小鼠心肌组织中ROS含量升高(
P
<
0.05),MDA、CAT、LD、LDH的水平显著增加(
P
<
0.01),SOD、GSH-Px、T-AOC的水平显著降低(
P
<
0.01),Nrf-2、HO-1、Bax、cleaved Caspase-3蛋白表达上调(
P
<
0.05,
P
<
0.01),Bcl-2蛋白表达下调(
P
<
0.05)。经BECH治疗后,能够显著降低低压低氧环境下小鼠的心肌组织氧化应激损伤(
P
<
0.01),显著降低LD的含量与LDH活性(
P
<
0.01),显著提高SOD、GSH-Px、T-AOC、LDH的水平(
P
<
0.01),上调Bcl-2、Nrf-2、HO-1的蛋白表达水平(
P
<
0.05,
P
<
0.01),下调Bax和cleaved Caspase-3蛋白表达(
P
<
0.05,
P
<
0.01),降低Bax/Bcl-2比值(
P
<
0.05)。
结论
2
BECH通过激活Nrf-2/HO-1信号通路,降低低压低氧小鼠心肌组织的氧化应激损伤,改善能量代谢,抑制细胞凋亡,进而缓解低压低氧诱导的心肌损伤。
Objective
2
To determine the protective effect of n-butanol extract of
Cremanthodium humile
(BECH) on myo
cardial damage induced by hypobaric hypoxia (HH) in mice.
Methods
2
Fifty clean-grade BALB/c male mice were divided into (
n
=10): hypoxia model group
acetazolamide group
low-
medium-and high-dose BECH groups (125
250 and 500 mg/kg) for normobaric confinement hypoxia experiments to determine the optimal dose of administration. Another 30 mice were divided into (
n
=10): acute decompression group
acetazolamide group and BECH administration group for the survival rate of the best administered dose in decompression hypoxia tolerance experiment. Fifty-two mice were divided into (
n
=13) normal control group
HH group
acetazolamide group and BECH administration group. BECH or acetazolamide was given intragastrically (i.g.) for 5 consecutive days
then the mice of the normal control group was placed at the local altitude
and those in the other groups were exposed to a simulated altitude of 8 000 m for 24 h in a hypobaric hypoxia chamber. After blood samples were harvested from the eyeball
all mice were sacrificed immediately. Histopathological changes in mouse myocardium were observed with HE staining. The serum activities of CK
AST and c-TnI were determined. The contents and levels of ROS
CAT
MDA
SOD
LD
LDH
GSH-Px and T-AOC in myocardial tissue were measured. Western blotting was used to detect the expression of Nrf-2
HO-1
Bax
Bcl-2 and cleaved Caspase-3 proteins in myocardial tissues.
Results
2
Compared with the hypoxia model group
BECH treatment significantly prolonged the survival time of mice in normobaric confinement hypoxia
especially the high-dose administration; the treatment also significantly reduced the mortality of mice in acute decompression. Significantly increased levels of ROS (
P
<
0.05) and MDA
CAT
LD and LDH (
P
<
0.01)
decreased levels of SOD
GSH-Px and T-AOC(
P
<
0.01)
up-regulation of Nrf-2
HO-1
Bax and cleaved C
aspase-3 (
P
<
0.05
P
<
0.01) and down-regulation of Bcl-2 (
P
<
0.05) in the myocardial tissues were observed in the mice from the HH model group than those in the control group. While
BECH treatment significantly attenuated myocardial tissue oxidative stress damage in mice under hypobaric hypoxic environment (
P
<
0.01)
decreased the amount of LD and the activity of LDH (
P
<
0.01)
increased the levels of SOD
GSH-Px and T-AOC(
P
<
0.01)
up-regulated the protein levels of Nrf-2
HO-1 amd Bcl-2(
P
<
0.05
P
<
0.01)
down-regulated those of Bax and cleaved Caspase-3 (
P
<
0.05
P
<
0.01)
and reduced the Bax/Bcl-2 ratio in myocardial tissue.
Conclusion
2
BECH inhibits oxidative stress
improves energy metabolism
suppresses cell apoptosis
via
activating the Nrf-2/HO-1 signaling pathway
and then ameliorates HH-induced myocardial tissue injury.
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