Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.

BACKGROUND: There are no drugs presently available to treat traumatic brain injury (TBI). A variety of single drugs have failed clinical trials suggesting a role for drug combinations. Drug combinations acting synergistically often provide the greatest combination of potency and safety. The drugs ex...

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Main Authors: Samah G Abdel Baki, Ben Schwab, Margalit Haber, André A Fenton, Peter J Bergold
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2930858?pdf=render
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spelling doaj-5e1492a8fc4d414396aa541ee044de232020-11-24T21:49:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-0158e1249010.1371/journal.pone.0012490Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.Samah G Abdel BakiBen SchwabMargalit HaberAndré A FentonPeter J BergoldBACKGROUND: There are no drugs presently available to treat traumatic brain injury (TBI). A variety of single drugs have failed clinical trials suggesting a role for drug combinations. Drug combinations acting synergistically often provide the greatest combination of potency and safety. The drugs examined (minocycline (MINO), N-acetylcysteine (NAC), simvastatin, cyclosporine A, and progesterone) had FDA-approval for uses other than TBI and limited brain injury in experimental TBI models. METHODOLOGY/PRINCIPAL FINDINGS: Drugs were dosed one hour after injury using the controlled cortical impact (CCI) TBI model in adult rats. One week later, drugs were tested for efficacy and drug combinations tested for synergy on a hierarchy of behavioral tests that included active place avoidance testing. As monotherapy, only MINO improved acquisition of the massed version of active place avoidance that required memory lasting less than two hours. MINO-treated animals, however, were impaired during the spaced version of the same avoidance task that required 24-hour memory retention. Co-administration of NAC with MINO synergistically improved spaced learning. Examination of brain histology 2 weeks after injury suggested that MINO plus NAC preserved white, but not grey matter, since lesion volume was unaffected, yet myelin loss was attenuated. When dosed 3 hours before injury, MINO plus NAC as single drugs had no effect on interleukin-1 formation; together they synergistically lowered interleukin-1 levels. This effect on interleukin-1 was not observed when the drugs were dosed one hour after injury. CONCLUSIONS/SIGNIFICANCE: These observations suggest a potentially valuable role for MINO plus NAC to treat TBI.http://europepmc.org/articles/PMC2930858?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Samah G Abdel Baki
Ben Schwab
Margalit Haber
André A Fenton
Peter J Bergold
spellingShingle Samah G Abdel Baki
Ben Schwab
Margalit Haber
André A Fenton
Peter J Bergold
Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
PLoS ONE
author_facet Samah G Abdel Baki
Ben Schwab
Margalit Haber
André A Fenton
Peter J Bergold
author_sort Samah G Abdel Baki
title Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
title_short Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
title_full Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
title_fullStr Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
title_full_unstemmed Minocycline synergizes with N-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
title_sort minocycline synergizes with n-acetylcysteine and improves cognition and memory following traumatic brain injury in rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-01-01
description BACKGROUND: There are no drugs presently available to treat traumatic brain injury (TBI). A variety of single drugs have failed clinical trials suggesting a role for drug combinations. Drug combinations acting synergistically often provide the greatest combination of potency and safety. The drugs examined (minocycline (MINO), N-acetylcysteine (NAC), simvastatin, cyclosporine A, and progesterone) had FDA-approval for uses other than TBI and limited brain injury in experimental TBI models. METHODOLOGY/PRINCIPAL FINDINGS: Drugs were dosed one hour after injury using the controlled cortical impact (CCI) TBI model in adult rats. One week later, drugs were tested for efficacy and drug combinations tested for synergy on a hierarchy of behavioral tests that included active place avoidance testing. As monotherapy, only MINO improved acquisition of the massed version of active place avoidance that required memory lasting less than two hours. MINO-treated animals, however, were impaired during the spaced version of the same avoidance task that required 24-hour memory retention. Co-administration of NAC with MINO synergistically improved spaced learning. Examination of brain histology 2 weeks after injury suggested that MINO plus NAC preserved white, but not grey matter, since lesion volume was unaffected, yet myelin loss was attenuated. When dosed 3 hours before injury, MINO plus NAC as single drugs had no effect on interleukin-1 formation; together they synergistically lowered interleukin-1 levels. This effect on interleukin-1 was not observed when the drugs were dosed one hour after injury. CONCLUSIONS/SIGNIFICANCE: These observations suggest a potentially valuable role for MINO plus NAC to treat TBI.
url http://europepmc.org/articles/PMC2930858?pdf=render
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