Abstract

The present study focused on secondary injury following the middle cerebral artery (MCA) occlusion in rats not linked to the MCA’s feeding zone. This entity has been very rarely studied. Additionally, this study investigated the rates of expression of five fundamental angiogenic biomarkers called endoglin, vascular endothelial growth factors-A (VEGF-A), endothelin-1 (ET-1), 2granulocyte colony-stimulating factor (G-CSF), and angiopoietin-using the MCA occlusion (MCAO) model. The random allocation of twelve adult male albino rats was in two groups. As a sham control group, six rats were used. This group was subjected to a sham operation without MCAO. The MCAO group consisted of six rats that were subjected to MCAO operation. After three days, the rats were sacrificed. The cerebellar specimens were immediately processed for light microscopic examination. An angiogenic biomarkers multiplex assay from multiplex was used to assess endoglin levels, VEGF-A, ET-1, angiopoietin-2, and G-CSF in serum samples. Hematoxylin and eosin-stained sections showed that the cerebellar cortex of rats of the MCAO group was more affected than the sham control group. Furthermore, Nissl stain and immunohistochemical analysis revealed an apparent increase in the number of positive immunoreactive in the cerebellar cortex and an evident decrease in Nissl granules in Purkinje cells of the MCAO rats, in contrast to the control rats. In addition, there was a significant increase in angiogenic factors VEGF-A, ET-1, angiopoietin-2, and endoglin. Interestingly, there was an increase in the G-CSF but a non-significant in the MCAO rats compared to the control rats. Furthermore, there was a significant correlation between the angiopoietin-2 and ET-1, and between G-CSF and ET-1. VEGF-A also exhibited significant positive correlations with the G-CSF serum level parameter, Endoglin, and ET-1. Rats subjected to MCAO are a suitable model to study secondary injury away from MCA’s feeding zone. Additionally, valuable insights into the association and interaction between altered angiogenic factors and acute ischemic stroke induced by MCAO in rats.

Highlights

  • Ischemic stroke is a severely impaired and high-incidence neurodegenerative condition

  • The current study aimed to focus on secondary injury following occlusion of the middle cerebral artery (MCA) in rats not linked to the feeding zone of the MCA

  • Aopoietin-2, Asection sectionshowing: showing: positive immunoreactive astrocytes endoglin, endothelin-1, and wereimmunoreactive investigated in the MCA occlusion (MCAO)(↑group ver positive immunoreactive astrocytes

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Summary

Introduction

Ischemic stroke is a severely impaired and high-incidence neurodegenerative condition. About 80% of all human strokes are ischemic strokes. They are caused by thrombotic and embolic occlusion that reduces or restricts blood flow in the MCA. The MCA is one of the main blood supplies in the brain [1]. About 15 million people suffer from strokes worldwide, according to the. Five million become permanently disabled, and five million die [2]. Stroke is becoming more and more of a critical health issue in the Middle

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