Effect of Bushen Jianpi Kaixin Formula on learning and cognitive ability and oxidative stress in the cerebral cortex of aging rats through the Keap1/Nrf2 pathway
Experimental Studies|更新时间:2023-10-09
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Effect of Bushen Jianpi Kaixin Formula on learning and cognitive ability and oxidative stress in the cerebral cortex of aging rats through the Keap1/Nrf2 pathway
Journal of Beijing University of Traditional Chinese MedicineVol. 46, Issue 9, Pages: 1250-1257(2023)
作者机构:
湖北中医药大学基础医学院 武汉 430065
作者简介:
Prof. KONG Mingwang, Ph. D., Doctoral Supervisor. School of Basic Medicine, Hubei University of Chinese Medicine, No. 16, West Huangjiahu Road, Wuchang District, Wuhan 430065. E-mail: 13349959661@163.com
基金信息:
National Key R&D Program "Research on the Modernization of Traditional Chinese Medicine"(2019YFC1708502)
LI Ying, WANG Ying, LIU Lin, et al. Effect of Bushen Jianpi Kaixin Formula on learning and cognitive ability and oxidative stress in the cerebral cortex of aging rats through the Keap1/Nrf2 pathway[J]. Journal of beijing university of traditional chinese medicine, 2023, 46(9): 1250-1257.
DOI:
LI Ying, WANG Ying, LIU Lin, et al. Effect of Bushen Jianpi Kaixin Formula on learning and cognitive ability and oxidative stress in the cerebral cortex of aging rats through the Keap1/Nrf2 pathway[J]. Journal of beijing university of traditional chinese medicine, 2023, 46(9): 1250-1257. DOI: 10.3969/j.issn.1006-2157.2023.09.010.
Effect of Bushen Jianpi Kaixin Formula on learning and cognitive ability and oxidative stress in the cerebral cortex of aging rats through the Keap1/Nrf2 pathway
and oxidative stress in the cerebral cortex of aging rats
and to explore its mechanism.
Methods
2
According to the random number table method
47 Sprague-Dawley rats were randomly divided into the blank group(
n
=10) and the modeling group(
n
=37). The rats in the modeling group were injected with D-galactose normal saline solution(300 mg/kg) for 6 weeks to establish the aging rat model. After successful modeling
according to the random number table method
30 aging rats were randomly divided into the model group
BJKF group and vitamin E group
with 10 rats each group. The rats in the BJKF group were treated with BJKF(9.99 g/kg) by gavage
the rats in the vitamin E group were treated with vitamin E(13.5 mg/kg) by gavage
and the rats in the blank group and the model group were treated with the same volume of normal saline by gavage. All the interventions were administered once daily for 4 weeks. After the intervention
the learning and memory abilities of rats were detected by the Morris water maze test. The cognitive function of rats was detected by the open-field test. The activity of superoxide dismutase(SOD) was detected by the WST-1 method. The content of malondialdehyde(MDA) was determined by TBA method. The hydroxyl radical inhibition ability was detected by colorimetry. The positive expression of Caspase-1 in the cerebral cortex was detected by immunohistochemistry. And the mRNA expressions of Keap1
Nrf2
NQO1 and HO-1 were detected by real-time PCR.
Results
2
Compared with the blank group
the evasion latency was prolonged from the third day(
P
<
0.05
P
<
0.01)
the number of plateau crossing was decreased(
P
<
0.01)
the movement distance and the time ratio of central area movement were decreased (
P
<
0.01)
the SOD activity and the hydroxyl radical inhibition ability were decreased(
P
<
0.01)
the expression of MDA was increased (
P
<
0.01)
the positive expression of Caspase-1 was increased(
P
<
0.01)
the mRNA expression of Keap1 was increased(
P
<
0.01)
and the mRNA expressions of Nrf2
NQO1
and HO-1 were decreased(
P
<
0.05
P
<
0.01) in the model group. Compared with the model group
the evasion latency was shortened on the fourth and fifth day(
P
<
0.05
P
<
0.01)
the number of plateau crossing was increased(
P
<
0.01)
the movement distance and the time ratio of central area movement were increased (
P
<
0.01)
the SOD activity and the hydroxyl radical inhibition ability were increased(
P
<
0.01)
the expression of MDA was decreased(
P
<
0.01)
the positive expression of Caspase-1 was decreased(
P
<
0.01)
the mRNA expression of Keap1 was decreased(
P
<
0.01)
while the mRNA expressions of Nrf2 and HO-1 were increased(
P
<
0.05
P
<
0.01) in the BJKF group.
Conclusion
2
BJKF can improve cognitive impairment and delay aging in aging rats whose mechanism is thought to be related to regulating oxidative stress.
关键词
Keywords
references
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