Evidence map›Paper›PMID 42835718›Full record

ArticlePhotoacoustics2026

Transcranial photoacoustic imaging of indocyanine green J-aggregates reveals cerebral signal changes in lipopolysaccharide-induced systemic inflammation.

Filip J Bodera, Elizabeth Berndl, Shrishti Singh, Anthony Tay, Greeshma Tarimala, Samuel K Jensen, Parag V Chitnis, Remi Veneziano, Mark J McVey, Michael C Kolios

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Article in Photoacoustics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Filip J BoderaDepartment of Physics, Toronto Metropolitan University, Toronto, Canada.
Elizabeth BerndlDepartment of Physics, Toronto Metropolitan University, Toronto, Canada.
Shrishti SinghDepartment of Bioengineering, George Mason University, Fairfax, VA, 22030, United States.
Anthony TayTranslational Medicine Program, The Hospital for Sick Children, Toronto, Canada.
Greeshma TarimalaDepartment of Chemical, Biochemical, and Environmental Engineering, University of Maryland, Baltimore County, United States.
Samuel K JensenTranslational Medicine Program, The Hospital for Sick Children, Toronto, Canada.
Parag V ChitnisDepartment of Bioengineering, George Mason University, Fairfax, VA, 22030, United States.
Remi VenezianoDepartment of Bioengineering, George Mason University, Fairfax, VA, 22030, United States.
Mark J McVeyDepartment of Physics, Toronto Metropolitan University, Toronto, Canada.
Michael C KoliosDepartment of Physics, Toronto Metropolitan University, Toronto, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic inflammation associated with surgery, infections, and trauma can damage organs, including the brain, and contribute to stroke and cognitive decline. Rapid assessment of inflammation-associated cerebrovascular changes remains difficult with existing neuroimaging modalities, particularly in settings requiring repeated or rapid measurements. Contrast-enhanced photoacoustic (PA) imaging may provide a research approach for monitoring cerebral vasculature. Objective: This pilot study investigated intracranial changes in dynamic PA signals of a novel photoacoustic imaging (PAI) tracer, non-encapsulated indocyanine green J-aggregates (J-aggs), in a model of lipopolysaccharide (LPS)-induced inflammation. This work is a pilot study to assess the potential of J-aggs for detecting systemic inflammation related changes in brain PAI signals. Methods: Systemic inflammation was induced in Sprague-Dawley rats with intraperitoneal (IP) LPS (3 mg/kg, n = 6) while sham rats received equal volume IP saline injections (n = 5). Transcranial PAI was performed before IP injections, 2-hours, and 4-hours after IP injections. Within the cerebral region of interest, P90 was defined as the mean PA signal intensity of voxels above the 90th-percentile intensity threshold, corresponding to the upper 10% of pixel values; group×time interactions were assessed using a linear mixed-effects model. Results: Intravenous J-aggs produced sustained PAI enhancement in sham rat brains (ΔP90(%) ~70% at 4-hours) whereas LPS-treated rats showed attenuated and more variable enhancement (ΔP90(%) ~30% at 4 h; group×time p = 0.0262). Reduced cerebral PA signal in LPS-treated rats may reflect altered J-aggs circulation or cerebral delivery, inflammation-related changes in cerebral blood volume, oxygenation, perfusion, or a combination of these factors. Conclusion: Because imaging was performed at a single wavelength of 890 nm, P90 represents a composite photoacoustic signal arising from J-aggs and endogenous hemoglobin; therefore, the attenuated response in LPS-treated rats may reflect altered J-aggs circulation or cerebral delivery, inflammation-related changes in cerebral blood volume or oxygenation, or a combination of these mechanisms.

Indexed as

CerebralContrastIndocyanineInflammationJ-aggregatesLipopolysaccharidePhotoacousticTranscranial

Identifiers

PMID42835718
PMCPMC13635703

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.