Diazoxide blocks or reduces microgliosis when applied prior or subsequent to motor neuron injury in mice.


Journal

Brain research
ISSN: 1872-6240
Titre abrégé: Brain Res
Pays: Netherlands
ID NLM: 0045503

Informations de publication

Date de publication:
15 08 2020
Historique:
received: 05 11 2019
revised: 23 04 2020
accepted: 04 05 2020
pubmed: 12 5 2020
medline: 2 9 2021
entrez: 12 5 2020
Statut: ppublish

Résumé

Diazoxide (DZX), an anti-hypertonic and anti-hypoglycemic drug, was shown to have anti-inflammatory effects in several injured cell types outside the central nervous system. In the brain, the neuroprotective potential of DZX is well described, however, its anticipated anti-inflammatory effect after acute injury has not been systematically analyzed. To disclose the anti-inflammatory effect of DZX in the central nervous system, an injury was induced in the hypoglossal and facial nuclei and in the oculomotor nucleus by unilateral axonal transection and unilateral target deprivation (enucleation), respectively. On the fourth day after surgery, microglial analysis was performed on tissue in which microglia were DAB-labeled and motoneurons were labeled with immunofluorescence. DZX treatment was given either prophylactically, starting 7 days prior to the injury and continuing until the animals were sacrificed, or postoperatively only, with daily intraperitoneal injections (1.25 mg/kg; in 10 mg/ml dimethyl sulfoxide in distilled water). Prophylactically + postoperatively applied DZX completely eliminated the microglial reaction in each motor nuclei. If DZX was applied only postoperatively, some microglial activation could be detected, but its magnitude was still significantly smaller than the non-DZX-treated controls. The effect of DZX could also be demonstrated through an extended period, as tested in the hypoglossal nucleus on day 7 after the operation. Neuronal counts, determined at day 4 after the operation in the hypoglossal nucleus, demonstrated no loss of motor neurons, however, an increased Feret's diameter of mitochondria could be measured, suggesting increased oxidative stress in the injured cells. The increase of mitochondrial Feret's diameter could also be prevented with DZX treatment.

Identifiants

pubmed: 32389588
pii: S0006-8993(20)30231-6
doi: 10.1016/j.brainres.2020.146875
pii:
doi:

Substances chimiques

Vasodilator Agents 0
Diazoxide O5CB12L4FN

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

146875

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Bernat Nogradi (B)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary; Foundation for the Future of Biomedical Sciences in Szeged, Szeged Scientists Academy, Pálfy u. 52/d, 6725 Szeged, Hungary.

Valeria Meszlenyi (V)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary; Foundation for the Future of Biomedical Sciences in Szeged, Szeged Scientists Academy, Pálfy u. 52/d, 6725 Szeged, Hungary.

Roland Patai (R)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary.

Tamas F Polgar (TF)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary.

Krisztina Spisak (K)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary.

Rebeka Kristof (R)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary.

Laszlo Siklos (L)

Institute of Biophysics, Biological Research Centre, Szeged, Temesvári krt. 62, 6726 Szeged, Hungary. Electronic address: siklos.laszlo@brc.hu.

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Classifications MeSH