1. Academic Validation
  2. Fruquintinib/HMPL-013 ameliorates cognitive impairments and pathology in a mouse model of cerebral amyloid angiopathy (CAA)

Fruquintinib/HMPL-013 ameliorates cognitive impairments and pathology in a mouse model of cerebral amyloid angiopathy (CAA)

  • Eur J Pharmacol. 2022 Dec 2;175446. doi: 10.1016/j.ejphar.2022.175446.
Guijuan Zhou 1 Tao Xiang 2 Yan Xu 2 Bing He 2 Lin Wu 2 Guanghua Zhu 2 Juan Xie 2 Lan Yao 2 Zijian Xiao 3
Affiliations

Affiliations

  • 1 Department of Neurology, The First Affiliated Hospital, University of South China, Hengyang, 421001, China; Department of Rehabilitation Medicine, The First Affiliated Hospital, University of South China, Hengyang, 421001, China.
  • 2 Department of Neurology, The First Affiliated Hospital, University of South China, Hengyang, 421001, China.
  • 3 Department of Neurology, The First Affiliated Hospital, University of South China, Hengyang, 421001, China. Electronic address: xiaozijian_edu@yeah.net.
Abstract

Cerebral amyloid angiopathy (CAA) is characterized by the cerebrovascular Amyloid-β (Aβ) accumulation, and always accompanied by Alzheimer's disease (AD). The mechanisms revealing CAA pathogenesis are still unclear, and it is challenging to develop an efficient therapeutic strategy for its treatment. Vascular endothelial growth factor (VEGF) and its receptors including VEGFR-1,-2,-3 activation are involved in Aβ processing, and modulate numerous cellular events associated with central nervous system (CNS) diseases. In the present study, we attempted to explore the regulatory function of fruquintinib (also named as HMPL-013), a highly selective inhibitor of VEGFR-1,-2,-3 tyrosine kinases, on CAA progression in Tg-SwDI mice. Here, we found that HMPL-013-rich diet consumption for 12 months significantly improved the behavioral performances and cerebral blood flow (CBF) of Tg-SwDI mice compared with the vehicle group. Importantly, HMPL-013 administration considerably reduced Aβ1-40 and Aβ1-42 burden in cortex and hippocampus of Tg-SwDI mice through regulating Aβ metabolism process. Congo red staining confirmed Aβ deposition in vessel walls, reflecting CAA formation, which was, however, strongly ameliorated after HMPL-013 treatment. Neuron death, aberrant glial activation and pro-inflammatory response in brain tissues of Tg-SwDI mice were dramatically alleviated after HMPL-013 consumption. More studies showed that the protective effects of HMPL-013 against CAA might be partially attributed to its regulation on the expression of genes associated with blood vasculature. Intriguingly, VEGF and phosphorylated VEGFR-1,-2 protein expression levels were remarkably decreased by HMPL-013 in cortex and hippocampus of Tg-SwDI mice, which were validated in HMPL-013-treated brain vascular endothelial cells (BVECs) under hypoxia. Finally, we found that VEGF-induced human umbilical vein endothelial cells (HUVEC) proliferation and tube formation were strongly abolished upon HMPL-013 exposure. Collectively, all these findings demonstrated that oral administration of HMPL-013 had therapeutic potential against CAA by reducing Aβ deposition, inflammation and neuron death via suppressing VEGF/VEGFR-1,-2 signaling.

Keywords

Aβ metabolism; Cerebral amyloid angiopathy (CAA); HMPL-013; Inflammation and neuron death; VEGF/VEGFR-1,-2.

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