AI Article Synopsis

  • The study investigates the effects of granulocyte colony stimulating factor (G-CSF) and neurotrophin receptor (NTR) on brain damage caused by cerebral ischemia-reperfusion injury in rats.
  • Rat models with focal middle cerebral artery occlusion were treated and compared to control groups, measuring infarct volume and motor function as well as conducting various assays to assess effects on inflammation and cell survival.
  • Results showed that G-CSF and NTR treatment significantly reduced brain injury, improved motor skills, and altered key inflammatory and anti-apoptotic markers, indicating their potential for promoting neuron regeneration and protective effects in ischemic conditions.

Article Abstract

Objective: To study the therapeutic effect and protective mechanism of granulocyte colony stimulating factor (G-CSF) and neurotrophin receptor (NTR) on cerebral ischemia-reperfusion injury.

Methods: Rat models of permanent focal middle cerebral artery occlusion (MCAO) were constructed by using a modified suture method, and the rats were assigned into three groups such as treatment group (the rats were injected with mixed G-CSF and NTR once), sham operation group and PBS control group. The volume of the cerebral infarction was detected using Triphenyltetrazolium Chloride (TTC) staining method; the motor function in rats was evaluated; and qRT-PCR detection, double immunofluorescence histochemistry and immunohistochemistry were performed to observe various effects.

Results: After G-CSF and NTR treatment, the infarct volume induced by MCAO in the treatment group was significantly lower than that in the PBS control group (<0.05). The motor function in the treatment group was significantly improved on day 7 and day 14 compared to the PBS control group (<0.05). The levels of MCP-1, TNF-, TGF-β and IL-10 mRNA in the treatment group decreased by 22% compared with PBS control group, and the difference was statistically significant (<0.05). The Bcl-2 protein level in the treatment group was greater than that in the PBS control group, while the Bax level in the treatment group was lower than in the control group; and both the differences were statistically significant (<0.05). The number of BrdU + cells in the treatment group was significantly greater than that in the PBS control group (<0.05).

Conclusion: G-CSF can promote the regeneration of neurons, promote the formation of new blood vessels, promote the reconstruction of neural network in rat MCAO models through anti apoptosis, anti-inflammation and mobilization of bone marrow hematopoietic cells to exert its powerful protective effect on neurons, and contribute to the repair of neural function and improvement of prognosis.

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