Aim
The objective is to characterize the modification of cerebral vasculature and tissue induced by soluble AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> abundantly present in the glymphatic clearance system. Approach: Aβ1−42Aβ1-42<math><mrow><mi>A</mi> <msub><mi>β</mi> <mrow><mn>1</mn> <mo>-</mo> <mn>42</mn></mrow> </msub> </mrow> </math> peptide was injected intracerebroventricularly and swept-source optical coherence tomography (SS-OCT) was used to monitor the progression of changes in the brain microvascular network and tissue in vivo over 14 days. Parameters reflecting vascular morphology and structure as well as tissue status were quantified and compared before treatment.
Conclusions
AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> burden in the glymphatic system directly contributes to cerebrovascular structural and morphological abnormalities and global brain tissue damage, suggesting severe deleterious properties of soluble cerebrospinal fluid- AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> . We also show that OCT can be used as an effective tool to monitor cerebrovascular dynamics and tissue property changes in response to therapeutic treatments in drug discovery research.
Results
Vascular perfusion density, vessel length, and branch density decreased sharply and persistently following peptide administration. In comparison, vascular average diameter and vascular tortuosity were moderately increased at the late stage of monitoring. Endpoint density gradually increased, and the global optical attenuation coefficient value decreased significantly over time. Conclusions: AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> burden in the glymphatic system directly contributes to cerebrovascular structural and morphological abnormalities and global brain tissue damage, suggesting severe deleterious properties of soluble cerebrospinal fluid- AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> . We also show that OCT can be used as an effective tool to monitor cerebrovascular dynamics and tissue property changes in response to therapeutic treatments in drug discovery research.
Significance
Antiamyloid ββ<math><mrow><mi>β</mi></mrow> </math> ( AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> ) immunotherapy is a promising therapeutic strategy for Alzheimer's disease (AD) but generates large amounts of soluble AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> peptides that could overwhelm the clearance pathway, leading to serious side effects. Direct implications of AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> in glymphatic drainage transport for cerebral vasculature and tissue are not well known. Studies are needed to resolve this issue and pave the way to better monitoring abnormal vascular events that may occur in AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> -modifying therapies for AD. Aim: The objective is to characterize the modification of cerebral vasculature and tissue induced by soluble AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> abundantly present in the glymphatic clearance system. Approach: Aβ1−42Aβ1-42<math><mrow><mi>A</mi> <msub><mi>β</mi> <mrow><mn>1</mn> <mo>-</mo> <mn>42</mn></mrow> </msub> </mrow> </math> peptide was injected intracerebroventricularly and swept-source optical coherence tomography (SS-OCT) was used to monitor the progression of changes in the brain microvascular network and tissue in vivo over 14 days. Parameters reflecting vascular morphology and structure as well as tissue status were quantified and compared before treatment. Results: Vascular perfusion density, vessel length, and branch density decreased sharply and persistently following peptide administration. In comparison, vascular average diameter and vascular tortuosity were moderately increased at the late stage of monitoring. Endpoint density gradually increased, and the global optical attenuation coefficient value decreased significantly over time. Conclusions: AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> burden in the glymphatic system directly contributes to cerebrovascular structural and morphological abnormalities and global brain tissue damage, suggesting severe deleterious properties of soluble cerebrospinal fluid- AβAβ<math><mrow><mi>A</mi> <mi>β</mi></mrow> </math> . We also show that OCT can be used as an effective tool to monitor cerebrovascular dynamics and tissue property changes in response to therapeutic treatments in drug discovery research.