Abstract

Vascular alterations emerge as a common denominator for several neurodegenerative diseases. In Parkinson’s disease (PD), a number of observations have been made suggesting that the occurrence of vascular pathology is an important pathophysiological aspect of the disease. Specifically, pathological activation of pericytes, blood-brain barrier (BBB) disruption, pathological angiogenesis and vascular regression have been reported. This review summarizes the current evidence for the different vascular alterations in patients with PD and in animal models of PD. We suggest a possible sequence of vascular pathology in PD ranging from early pericyte activation and BBB leakage to an attempt for compensatory angiogenesis and finally vascular rarefication. We highlight different pathogenetic mechanisms that play a role in these vascular alterations including perivascular inflammation and concomitant metabolic disease. Awareness of the contribution of vascular events to the pathogenesis of PD may allow the identification of targets to modulate those mechanisms. In particular the BBB has for decades only been viewed as an obstacle for drug delivery, however, preservation of its integrity and/or modulation of the signaling at this interface between the blood and the brain may prove to be a new avenue to take in order to develop disease-modifying strategies for neurodegenerative disorders.

Highlights

  • This review summarizes the current evidence for the different vascular alterations in patients with Parkinson’s disease (PD) and in animal models of PD

  • We suggest a possible sequence of vascular pathology in PD ranging from early pericyte activation and blood-brain barrier (BBB) leakage to an attempt for compensatory angiogenesis and vascular rarefication

  • Angiogenic Molecules Findings indicating angiogenesis in PD are supported by reports showing an upregulation of the pro-angiogenic molecule Vascular Endothelial Growth Factor (VEGF) in the substantia nigra pars compacta (SNpc) of PD patients (Wada et al, 2006; Yasuda et al, 2007; Lan et al, 2021) and non-human primates (Barcia et al, 2005)

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Summary

BRAIN VASCULATURE

The brain is a highly oxygen consuming organ and, as a result, has developed a dense network of almost 650 km of microvessels (Pandey et al, 2016). The smallest entity is formed by capillaries that are in close contact with the surrounding parenchyma and allow the gas exchange. This close connection between blood and brain is termed the neurovascular unit (NVU). The NVU consists of endothelial cells, pericytes and the basal lamina forming the microcapillary wall, and cells in the immediate surrounding brain parenchyma including perivascular astrocytes, perivascular microglia and neurons

Blood Vessels as Adaptors of Blood Flow
Microvasculature in PD
Blood Vessels as Communicators of Signals
Vascular Regression
Inflammation and Vascular Pathology
DISCUSSION AND OUTLOOK
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