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239
alzheimers disease, AD
90 SD
15 - 1-42(A1-42) AD
1
0.81.6 3.2 g/kg 0.02 mg/kg
30 dSOD
GSH-PxMDA
[(239.0548.42)s(214.3574.52)s (97.3930.69sP 0.01]
[(1.933.25)(2.273.09)(6.623.45)P 0.05]
SOD[(177.2763.10)U/mg(164.5372.58)U/mg (72.5621.04)U/mgP 0.01] GSH-Px
[(2 899.36362.27)U/g(2 407.68472.14)U/g (1 397.64442.17)U/gP 0.01]
MDA [(24.759.94)nmol/mg(27.745.82)nmol/mg (37.5617.23)nmol/mgP 0.01]
AD
Effects of Tianqi-Yizhi granules on oxidative stress in the brain tissue, and learning and
memory in Alzheimer's disease model rats Zhao Jun*, Wu Yiming, Ma Tao, Wei Dongfeng.
*
Worker Hospital of Xuanhua Steel Company, Hebei Iron & Steel Group, Zhangjiakou 075100, China
Corresponding author: Ma Tao, Dongfang Hospital Affiliated to Beijing University of Chinese Medicine,
Beijing 100078, China; Email: matao327@126.com
Abstract
Objective
brain tissue, and learning and memory in Alzheimer's disease model rats. Methods A total of 90 male SD rats
were randomly divided into 6 groups by random number table method: sham operation group, model group,
huperzine A group and groups of low-, medium- and high-dose Tianqi-Yizhi granules, with 15 rats in each
group. The AD rat model was prepared by the left lateral ventricle injection of amyloid-1-42. One week after
modeling, the rats in the groups of low-, medium- and high-dose Tianqi-Yizhi granules received intragastric
administration of 0.8, 1.6 and 3.2 g/kg Tianqi-Yizhi granules, respectively; the rats in the huperzine A group
received intragastric administration of 0.02 mg/kg huperzine A solution; and the rats in the sham operation and
model groups received intragastric administration of equivalent volume of normal saline for 30 days. Learning
and memory were evaluated using the dark avoidance test. The activities of superoxide dismutase (SOD) and
glutathione peroxidase (GSH-Px), and malonaldehyde (MDA) level in the brain tissue were determined.
Results
In comparison with the model group, the latencies to step into the dark chamber in the high- and
DOI: 10.3760/cma.j.issn.1673-4246.2015.03.013
2013ZX09103002-002
81430100
075100 100078
100875
Email: matao327@126.com
240 20153373 Int J Trad Chin Med, March 2015, Vol. 37, No.3
medium-dose Tianqi-Yizhi granules groups were significantly longer (239.05 48.42 s, 214.35 74.52 s vs.
97.39 30.69 s; all P<0.01), the numbers of errors significantly decreased (1.93 3.25, 2.27 3.09 vs. 6.62
3.45; all P<0.05), the activities of SOD (177.27 63.10 U/mg, 164.53 72.58 U/mg vs. 72.5621.04 U/mg; all
P<0.01) and GSH-Px (2 899.36 362.27 U/g, 2 407.68 472.14 U/g vs. 1 397.64 442.17 U/g; all P<0.01),
and MDA level (24.75 9.94 nmol/mg, 27.74 5.82 nmol/mg vs. 37.56 17.23 nmol/mg; all P<0.01) in the
brain tissue significantly increased. Conclusion
Alzheimers disease, AD
2013112020140504SOD
AD
GSH-PX
MDA
AD
20140401
2014032520140305
AD AD
AD
1.3
[1]
DBA-2
AD
5810R
Eppendorf Ultrospec
[2-3]
AD
1.4
AD -(amyloid-, A)1-42
1 mg A1-42
AD AD
DMSO
[4]
4 24 h 10%
SPF SD 4
250300 g
SCXK2009-0015SPF
0.8 mm 1.5 mm
21340
3.5 mm A1-42
5% 12 h
5 l 1 l/min
1.2
5 min
20140913
6.4 g /g
130814AA1-42
1.5
CL-05-00776Sigma-Aldrich
RIPA BCA
15
90 SD
20153373 Int J Trad Chin Med, March 2015, Vol. 37, No.3
241
A1-42 AD
3.21.60.8 g/kg
0.05 P0.01
0.02 mg/kg
30 d
0.05 1
1.6
2 h
1 5 min
(mg/kg)
(s)
()
15
276.3459.29
0.731.21
15
97.3930.69a
6.623.45a
15
0.02
225.8269.03b
1.723.90c
15
3 200
239.0548.42
1.933.25c
15
1 600
214.3574.52b
2.273.09c
15
800
194.2133.04b
5.432.32
24 h
1.7
( x s )
aP0.01bP0.01cP0.05
RIPA 4
10 000 r/min BCA
2.2
SODGSH-PX
SOD
MDA
GSH-PX MDA
1.8
SPSS13.0
P0.01
x s one-way
SODGSH-PX MDA
P0.05 P
0.01
2
2.1
30 d
P0.01
A1-42
SODMDAGSH-PX ( x s )
(mg/kg)
SOD (U/mg)
MDA(nmol/mg)
243.2647.65
72.5621.04a
37.5617.23a
146.0354.04
33.4214.05
1 647.05329.77
177.2763.10
24.75 9.94
2 899.36362.27b
164.5372.58
27.74 5.82
2 407.68472.14b
132.4969.14
35.05 9.43
2 409.39448.93b
6
6
6
0.02
3 200
1 600
800
22.63 8.86
GSH-PX (U/g)
3 572.12543.29
1 397.64442.17a
SODMDAGSH-PXaP0.01bP0.01cP0.05
242 20153373 Int J Trad Chin Med, March 2015, Vol. 37, No.3
AD
A1-42
AD
AD
AD
AD
5
[ ]
SODGSH-PX
Neurol,2001,60(8):759-767.
6
Neurosci,2014,34(42):14022-14031.
8
A1-42 AD
3-4 AD
[
AD 8-9
[
[6-7]
. [M]. 4 .
,2010:686.
AD A
AD A 7 A
,. Alzheimer
[J]. ,2011,42(9):5-7.
[6]
AD A
.
[J]. ,2011,52(19):1627-1629.
peptide
oligomer-induced
synaptotoxicity
and
2014-11-05