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DOI 10.1016/j.drugalcdep.2019.107637

Медицинская библиотека · Drug and alcohol dependence · 2019

Acute cocaine administration alters permeability of blood-brain barrier in freely-moving rats- Evidence using miniaturized fluorescence microscopy.

Barr Jeffrey L, Brailoiu G Cristina, Abood Mary E, Rawls Scott M, Unterwald Ellen M, Brailoiu Eugen

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

BACKGROUND

Cocaine has a variety of negative effects on the central nervous system, including reports of decreased barrier function of brain microvascular endothelial cells. However, few studies have directly shown the effects of cocaine on blood-brain barrier (BBB) function in vivo. The miniature integrated fluorescence microscope (i.e., miniscope) technology was used to visualize cocaine-induced changes in BBB permeability in awake, freely-moving rats.

METHODS

The miniscope was implanted in the prefrontal cortex of adult male rats. After recovery and acclimation, rats received an injection of cocaine (5-20 mg/kg ip) 15 minutes following iv infusion of sodium fluorescein, a low molecular weight tracer. Fluorescence intensity was recordedin vivo via the miniscope for 30 minutes or 24 hours post cocaine administration and served as an indicator of BBB permeability.

RESULTS

Results demonstrate that cocaine increased the sodium fluorescein extravasation in brain microcirculation in a dose-dependent manner 30 minutes, but not 24 hours after administration.

CONCLUSION

We report for the first time using direct visualization of brain microcirculation with the miniscope technology in awake, freely-moving rats, that acute cocaine administration produced a transient increase in the BBB permeability.

Для цитирования: Barr Jeffrey L, Brailoiu G Cristina, Abood Mary E, Rawls Scott M, Unterwald Ellen M, Brailoiu Eugen. Acute cocaine administration alters permeability of blood-brain barrier in freely-moving rats- Evidence using miniaturized fluorescence microscopy.. Drug and alcohol dependence. 2019. DOI: 10.1016/j.drugalcdep.2019.107637.

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