Topological functional network analysis of cortical blood flow in hyperacute ischemic rats.

Abstract

Acute cerebral ischemia alters brain network connectivity, leading to notable increases in both anatomical and functional connectivity while observing a reduction in metabolic connectivity. However, alterations of the cerebral blood flow (CBF) based functional connectivity remain unclear. We collected continuous CBF images using laser speckle contrast imaging (LSCI) technology to monitor ischemic occlusion-reperfusion progression through occlusion of the left carotid artery. We also used a dense cortical grid atlas to construct CBF-based functional connectivity networks for hyperacute ischemic rodents. Graph theoretical analysis was used to measure network topological characteristics and construct topological connection graphs. Coactivation pattern (CAP) analysis was utilized to examine the spatiotemporal characteristics of the global network. Additionally, we measured evoked functional hyperemia and correlated it with network topologies. Network analysis indicated a significant increase in functional connectivity, global efficiency, local efficiency, small-worldness, clustering coefficient, and regional degree centrality primarily within the left ischemic intra-hemisphere, accompanied by weaker changes in the right intra-hemisphere. Inter-hemisphere networks exhibited reduced homologous connections, global efficiency, and small-worldness. CAP analysis revealed increased strength of the left negative activation brain network's state fraction of time and transition probability from equilibrium-to-imbalance states. Left network metrics declined following blood flow reperfusion. Furthermore, positive/negative correlations between barrel-evoked intensity and regional network topologies were reversed as negative/positive correlations after cerebral ischemia. These findings suggest a damaged CBF functional network mechanism following acute cerebral ischemia and a disrupted association between resting state and evoked hyperemia.