Evidence map›Paper›PMID 25614385›Full record

ReviewJournal of neuroscience methods2015

Experimental evaluation and computational modeling of tissue damage from low-flow push-pull perfusion sampling in vivo.

David E Cepeda, Leah Hains, David Li, Joseph Bull, Stephen I Lentz, Robert T Kennedy

Abstract readEvaluation StudyReview
In one paragraph

Review in Journal of neuroscience methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

David E CepedaUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Ave, Ann Arbor, MI, 49109, United States; University of Michigan, Department of Chemistry, 930N University Ave, Ann Arbor, MI, 48109, United States.
Leah HainsWadsworth Center, NYS Department of Health, New York State Bicycle Route 5, Albany, NY 12201, United States.
David LiUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Ave, Ann Arbor, MI, 49109, United States.
Joseph BullUniversity of Michigan, Department of Biomedical Engineering, 1101 Beal Ave, Ann Arbor, MI, 49109, United States.
Stephen I LentzUniversity of Michigan, Department of Internal Medicine, Division of Metabolism, Endocrinology & Diabetes, 6245 Brehm Tower, 1000 Wall Street, Ann Arbor, MI, 48105, United States.
Robert T KennedyUniversity of Michigan, Department of Chemistry, 930N University Ave, Ann Arbor, MI, 48109, United States. Electronic address: rtkenn@umich.edu.

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
In vivo chemical monitoring using capillary separationsR37EB003320 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2008 to 2017
$3.6M
NIBIB NIH HHS R37 EB003320NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30DK020572NIDDK NIH HHS P60 DK020572
6 · The paper itself

Abstract

backgroundNeurochemical monitoring via sampling probes is valuable for deciphering neurotransmission in vivo. Microdialysis is commonly used; however, the spatial resolution is poor. NEW

methodRecently push-pull perfusion at low flow rates (50nL/min) has been proposed as a method for in vivo sampling from the central nervous system. Tissue damage from such probes has not been investigated in detail. In this work, we evaluated acute tissue response to low-flow push-pull perfusion by infusing the nuclear stains Sytox Orange and Hoechst 33342 through probes implanted in the striatum for 200min, to label damaged and total cells, respectively, in situ.

resultsUsing the damaged/total labeled cell ratio as a measure of tissue damage, we found that 33±8% were damaged within the dye region around a microdialysis probe. We found that low-flow push-pull perfusion probes damaged 24±4% of cells in the sampling area. Flow had no effect on the number of damaged cells for low-flow push-pull perfusion. Modeling revealed that shear stress and pressure gradients generated by the flow were lower than thresholds expected to cause damage. Comparison with existing methods.Push-pull perfusion caused less tissue damage but yielded 1500-fold better spatial resolution.

conclusionsPush-pull perfusion at low flow rates is a viable method for sampling from the brain with potential for high temporal and spatial resolution. Tissue damage is mostly caused by probe insertion. Smaller probes may yield even lower damage.

Indexed as

AnimalsBenzimidazolesCell CountCell SurvivalComputer SimulationCorpus StriatumEquipment DesignMaleMicrodialysisMicroscopy, ConfocalMicroscopy, FluorescenceOrganic ChemicalsPerfusionPressureRats, Sprague-DawleyBenzimidazolesbisbenzimide ethoxide trihydrochlorideOrganic ChemicalsSYTOX Orange dyeBrain tissue damageCell viabilityComputational modelingIn vivo samplingMicrodialysisPush–pull perfusion

Identifiers

PMID25614385
PMCPMC4331210

What OpenQuestion holds

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Registered trials

None linked

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.