Evidence map›Paper›PMID 10751025›Full record

ArticlePharmaceutical research2000

An isolated in-situ rat head perfusion model for pharmacokinetic studies.

K A Foster, G D Mellick, M Weiss, M S Roberts

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Article in Pharmaceutical research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Cytochrome P450-mediated drug metabolism in the brain.Journal of psychiatry & neuroscience : JPN · 2013
    Review
  2. Drug structure-transport relationships.Journal of pharmacokinetics and pharmacodynamics · 2010
    Review
  3. Article
  4. Article
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

4 authors.

K A FosterDepartment of Medicine, University of Queensland, Princess Alexandra Hospital, Woolloongabba, Australia.
G D Mellick
M Weiss
M S Roberts

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo develop a viable, single pass rat head perfusion model useful for pharmacokinetic studies.

methodsA viable rat head preparation, perfused with MOPS-buffered Ringer's solution, was developed. Radiolabelled markers (red blood cells, water and sucrose) were injected in a bolus into the internal carotid artery and collected from the posterior facial vein over 28 minutes. The double inverse Gaussian function was used to estimate the statistical moments of the markers.

resultsThe viability of the perfusion was up to one hour, with optimal perfusate being 2% bovine serum albumin at 37 degrees C, pH 7.4. The distribution volumes for red blood cells, sucrose and water (from all studies, n = 18) were 1.0 +/- 0.3 ml, 6.4 +/- 4.2 ml and 18.3 +/- 11.9 ml, respectively. A high normalised variance for red blood cells (3.1 +/- 2.0) suggests a marked vascular heterogeneity. A higher normalised variance for water (6.4 +/- 3.3) is consistent with additional diffusive/permeability limitations.

conclusionsAnalysis of the physiological parameters derived from the moments suggested that the kinetics of the markers were consistent with distribution throughout the head (weight 25 g) rather than just the brain (weight 2 g). This model should assist in studying solute pharmacokinetics in the head.

Indexed as

PerfusionAnimalsCarbon RadioisotopesCatheterizationCerebral ArteriesCerebral VeinsCerebrovascular CirculationCreatine KinaseDogsErythrocytesFemaleHeadHydrogen-Ion ConcentrationIn Vitro TechniquesL-Lactate DehydrogenaseNormal DistributionCarbon RadioisotopesCreatine KinaseL-Lactate DehydrogenaseSucroseTritiumWater

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Registered trials

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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.