Protective Effect of Acupuncture Serum Derived from Acute Convulsion Rats on Cultured Hippocampal Neurons with Seizure-like Discharges by Regulating Expression of Endoplasmic Reticulum Stress-inducible Molecular Chaperones
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Protective Effect of Acupuncture Serum Derived from Acute Convulsion Rats on Cultured Hippocampal Neurons with Seizure-like Discharges by Regulating Expression of Endoplasmic Reticulum Stress-inducible Molecular Chaperones
ZHANG Hui, YANG Fan, WU Xu, et al. Protective Effect of Acupuncture Serum Derived from Acute Convulsion Rats on Cultured Hippocampal Neurons with Seizure-like Discharges by Regulating Expression of Endoplasmic Reticulum Stress-inducible Molecular Chaperones[J]. Acupuncture research, 2017, 42(2): 95-101.
DOI:
ZHANG Hui, YANG Fan, WU Xu, et al. Protective Effect of Acupuncture Serum Derived from Acute Convulsion Rats on Cultured Hippocampal Neurons with Seizure-like Discharges by Regulating Expression of Endoplasmic Reticulum Stress-inducible Molecular Chaperones[J]. Acupuncture research, 2017, 42(2): 95-101. DOI: 10.13702/j.1000-0607.2017.02.001.
Protective Effect of Acupuncture Serum Derived from Acute Convulsion Rats on Cultured Hippocampal Neurons with Seizure-like Discharges by Regulating Expression of Endoplasmic Reticulum Stress-inducible Molecular Chaperones
Objective To observe the effect of acupuncture serum on the number of apoptosis of the cultured hippocampal neurons with seizure-like discharges and the expression levels of endoplasmic reticulum stress-inducible molecular chaperones glucose-regulated protein 78(GRP 78)
so as to reveal its protective mechanism on seizure-induced injury of hippocampal neurons.Methods A regular primary culture of neurons derived from the hippocampus of the newly-born SD rats was conducted for 10 days
then these cultured neurons that displayed seizure-like discharges in Mg
(2+)
-free medium were divided into normal extracellular fluid(medium)group(normal)
Mg(2+)-free medium were divided into normal extracellular fluid(medium)group(normal)
Mg
(2+)
-free medium group
acupuncture serum group and non-acupuncture serum group(n=30).Blood examples were taken from pentylenetetrazol(i.p.i.)-induced acute convulsion adult SD rats underwent manual acupuncture stimulation of"Baihui"(GV 20)and"Dazhui"(GV 14
once daily for 7days)to prepare acupuncture serum.Hippocampal neuronal cultures were prepared from hippocampal tissue isolated from 24h-old SD rats.The isolated neurons were incubated normally in Dulbecco's Modified Eagle Medium(DMEM)/Nutrient Mixture F 12(1∶1)for 10 days
followed by exposure to the extracellular fluid{composed of NaCl
D-glucose and aminoethanoic acid(pH 7.3)}for3hand returned to normal culture for normal group
by exposure to Mg(2+)-free medium group
acupuncture serum group and non-acupuncture serum group(n=30).Blood examples were taken from pentylenetetrazol(i.p.i.)-induced acute convulsion adult SD rats underwent manual acupuncture stimulation of"Baihui"(GV 20)and"Dazhui"(GV 14
once daily for 7days)to prepare acupuncture serum.Hippocampal neuronal cultures were prepared from hippocampal tissue isolated from 24h-old SD rats.The isolated neurons were incubated normally in Dulbecco's Modified Eagle Medium(DMEM)/Nutrient Mixture F 12(1∶1)for 10 days
followed by exposure to the extracellular fluid{composed of NaCl
D-glucose and aminoethanoic acid(pH 7.3)}for3hand returned to normal culture for normal group
by exposure to Mg
(2+)
-free extracellular fluid(to induce seizure-like discharges)for 3hand returned to normal culture for Mg(2+)-free extracellular fluid(to induce seizure-like discharges)for 3hand returned to normal culture for Mg
(2+)
-free medium group
by exposure to Mg(2+)-free medium group
by exposure to Mg
(2+)
-free extracellular fluid for 3hand returned to a regular culture medium [DMEM/F 12(1∶1)]plus acupuncture serum(9∶1)for acupuncture serum group
and by exposure to Mg(2+)-free extracellular fluid for 3hand returned to a regular culture medium [DMEM/F 12(1∶1)]
plus acupuncture serum(9∶1)for acupuncture serum group
and by exposure to Mg
(2+)
-free extracellular fluid for 3hand returned to DMEM/F 12(1∶1)plus non-acupuncture serum(9∶1)for non-acupuncture serum group.The cell apoptosis was assessed at 2
12 and 48hafter application of acupuncture serum or non-acupuncture serum by using TUNEL method and the expression levels of GRP 78
CHOP and Caspase-12 proteins of the cultured cells at the 3time-points detected using Western blot.Results The number of apoptotic hippocampal neurons was significantly higher in the Mg(2+)-free extracellular fluid for 3hand returned to DMEM/F 12(1∶1)plus non-acupuncture serum(9∶1)for non-acupuncture serum group.The cell apoptosis was assessed at 2
12 and 48hafter application of acupuncture serum or non-acupuncture serum by using TUNEL method and the expression levels of GRP 78
CHOP and Caspase-12 proteins of the cultured cells at the 3time-points detected using Western blot.Results The number of apoptotic hippocampal neurons was significantly higher in the Mg
(2+)
-free medium group than in the normal medium group at 2
12 and 48h(P
<
0.01)
and considerably decreased in the acupuncture serum group(but not in the non-acupuncture serum group)relevant to the Mg(2+)-free medium group than in the normal medium group at 2
12 and 48h(P
<
0.01)
and considerably decreased in the acupuncture serum group(but not in the non-acupuncture serum group)relevant to the Mg
(2+)
-free medium group at the same timepoints after application of acupuncture serum(P
<
0.05
P
<
0.01).The expression levels of GRP 78 protein at 2h
CHOP and Caspase-12 proteins at 2
12 and 48hwere significantly up-regulated in the Mg(2+)-free medium group at the same timepoints after application of acupuncture serum(P
<
0.05
P
<
0.01).The expression levels of GRP 78 protein at 2h
CHOP and Caspase-12 proteins at 2
12 and 48hwere significantly up-regulated in the Mg
(2+)
-free medium group relavant to the normal medium group(P
<
0.05
P
<
0.01).After application of acupuncture serum to the culture medium
the expression levels of GRP 78 protein at the three time-points were significantly increased in comparison with the Mg(2+)-free medium group relavant to the normal medium group(P
<
0.05
P
<
0.01).After application of acupuncture serum to the culture medium
the expression levels of GRP 78 protein at the three time-points were significantly increased in comparison with the Mg
(2+)
-free medium group(P
<
0.01
P
<
0.05)
while those of CHOP at 12 and 48 h
and Caspase-12 at the three time-points were notably down-regulated(P
<
0.05
P
<
0.01).No significant differences were found between the non-acupuncture serum and Mg(2+)-free medium group(P
<
0.01
P
<
0.05)
while those of CHOP at 12 and 48 h
and Caspase-12 at the three time-points were notably down-regulated(P
<
0.05
P
<
0.01).No significant differences were found between the non-acupuncture serum and Mg
(2+)
-free medium groups in the expression levels of GRP 78
CHOP and Caspase-12 proteins at the three time-points(P
>
0.05).Conclusion Acupuncture serum can significantly reduce apoptosis of the cultured hippocampal neurons
which may be related to its effects in increasing the expression of GRP 78 protein and down-regulating the expression of CHOP and Caspase-12 proteins
suggesting an important role of acupuncture serum in maintaining the stability of the neuronal endoplasmic reticulum.
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Effect of electroacupuncture on oxidative stress and cell apoptosis induced by ferroptosis in mice with Parkinson’s disease
Effect of electroacupuncture on behavior and cell apoptosis of brain tissue in traumatic brain injury rats
Effect of acupuncture serum on expression of microtubule associated protein-2 and nerve growth associated protein-43 in Mg~(2+)-free-cultured hippocampal neurons of neonatal rats
Effect of manual acupuncture of “Shuigou” (GV26)“Neiguan” (PC6) on neurological function and expression of apoptosis-related factors in brain tissues surrounding hematoma in intracerebral hemorrhage rats
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