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Melatonin reduces excitotoxic blood-brain barrier breakdown in neonatal rats

Moretti, R. (author)
Zanin, A. (author)
Pansiot, J. (author)
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Spiri, D. (author)
Manganozzi, L. (author)
Kratzer, I. (author)
Favero, G. (author)
Vasiljevic, A. (author)
Rinaldi, V. E. (author)
Pic, I. (author)
Massano, D. (author)
D'Agostino, I. (author)
Baburamani, Ana A (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
La Rocca, M. A. (author)
Rodella, L. F. (author)
Rezzani, R. (author)
Ek, C. Joakim (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
Strazielle, N. (author)
Ghersi-Egea, J. F. (author)
Gressens, P. (author)
Titomanlio, L. (author)
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 (creator_code:org_t)
Elsevier BV, 2015
2015
English.
In: Neuroscience. - : Elsevier BV. - 0306-4522. ; 311, s. 382-397
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The blood-brain barrier (BBB) is a complex structure that protects the central nervous system from peripheral insults. Understanding the molecular basis of BBB function and dysfunction holds significant potential for future strategies to prevent and treat neurological damage. The aim of our study was (1) to investigate BBB alterations following excitotoxicity and (2) to test the protective properties of melatonin.Ibotenate, a glutamate analog, was injected intracerebrally in postnatal day 5 (P5) rat pups to mimic excitotoxic injury. Animals were than randomly divided into two groups, one receiving intraperitoneal (i.p.) melatonin injections (5. mg/kg), and the other phosphate buffer saline (PBS) injections. Pups were sacrificed 2, 4 and 18. h after ibotenate injection. We determined lesion size at 5. days by histology, the location and organization of tight junction (TJ) proteins by immunohistochemical studies, and BBB leakage by dextran extravasation. Expression levels of BBB genes (TJs, efflux transporters and detoxification enzymes) were determined in the cortex and choroid plexus by quantitative PCR.Dextran extravasation was seen 2. h after the insult, suggesting a rapid BBB breakdown that was resolved by 4. h. Extravasation was significantly reduced in melatonin-treated pups. Gene expression and immunohistochemical assays showed dynamic BBB modifications during the first 4. h, partially prevented by melatonin. Lesion-size measurements confirmed white matter neuroprotection by melatonin.Our study is the first to evaluate BBB structure and function at a very early time point following excitotoxicity in neonates. Melatonin neuroprotects by preventing TJ modifications and BBB disruption at this early phase, before its previously demonstrated anti-inflammatory, antioxidant and axonal regrowth-promoting effects. © 2015 IBRO.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

Blood-brain barrier
Brain development
Ibotenate
Melatonin
Periventricular white matter damage

Publication and Content Type

ref (subject category)
art (subject category)

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