Impact of benzodiazepines on brain FDG-PET quantification after single-dose and chronic administration in rats

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• 作者：Jesú ; s Silva-Rodrí ; guez^a ; ¹ ; ^{jesus.silva@gmx.es" class="auth_mail" title="E-mail the corresponding author} ; Lara Garcí ; a-Varela^a ; ¹ ; Esteban Ló ; pez-Arias^b ; Iné ; s Domí ; nguez-Prado^c ; Julia Corté ; s^c ; Juan Pardo-Montero^a ; Anxo Fern&aacute ; ndez-Ferreiro^a ; &Aacute ; lvaro Ruibal^a ; ^c ; ^d ; ^e ; Tom&aacute ; s Sobrino^b ; Pablo Aguiar^a ; ^d
• 关键词：Pet ; Brain ; Preclinical ; Pharmacology ; Diazepam ; Benzodiazepines
• 刊名：Nuclear Medicine and Biology
• 出版年：2016
• 出版时间：December 2016
• 年：2016
• 卷：43
• 期：12
• 页码：827-834
• 全文大小：912 K

文摘

Current guidelines for brain PET imaging advice against the injection of diazepam prior to brain FDG-PET examination in order to avoid possible interactions of benzodiazepines with the radiotracer uptake. Nevertheless, many patients undergoing PET studies are likely to be under chronic treatment with benzodiazepines, for example due to the use of different medications such as sleeping pills. Animal studies may provide an extensive and accurate estimation of the effect of benzodiazepines on brain metabolism in a well-defined and controlled framework.

Aim

This study aims at evaluating the impact of benzodiazepines on brain FDG uptake after single-dose administration and chronic treatment in rats.

Methods

Twelve Sprague–Dawley healthy rats were randomly divided into two groups, one treated with diazepam and the other used as control group. Both groups underwent PET/CT examinations after single-dose and chronic administration of diazepam (treated) or saline (controls) during twenty-eight days. Different atlas-based quantification methods were used to explore differences on the total uptake and uptake patterns of FDG between both groups.

Results

Our analysis revealed a significant reduction of global FDG uptake after acute (−16.2%) and chronic (−23.2%) administration of diazepam. Moreover, a strong trend pointing to differences between acute and chronic administrations (p < 0.08) was also observed. Uptake levels returned to normal after interrupting the administration of diazepam. On the other hand, patterns of FDG uptake were not affected by the administration of diazepam.

Conclusions

The administration of diazepam causes a progressive decrease of the FDG global uptake in the rat brain, but it does not change local patterns within the brain. Under these conditions, visual assessment and quantification methods based on regional differences such as asymmetry indexes or SPM statistical analysis would still be valid when administrating this medication.