-
Je něco špatně v tomto záznamu ?
Chronic citalopram effects on the brain neurochemical profile and perfusion in a rat model of depression detected by the NMR techniques - spectroscopy and perfusion
I. Harastova-Pavlova, E. Drazanova, L. Kratka, P. Amchova, M. Hrickova, O. Macicek, J. Vitous, R. Jirik, J. Ruda-Kucerova
Jazyk angličtina Země Francie
Typ dokumentu časopisecké články
- MeSH
- bulbus olfactorius metabolismus chirurgie účinky léků MeSH
- citalopram * farmakologie MeSH
- deprese farmakoterapie metabolismus MeSH
- depresivní porucha unipolární farmakoterapie metabolismus MeSH
- hipokampus metabolismus účinky léků MeSH
- krysa rodu rattus MeSH
- magnetická rezonanční spektroskopie metody MeSH
- modely nemocí na zvířatech * MeSH
- mozek * metabolismus účinky léků MeSH
- mozkový krevní oběh * účinky léků MeSH
- potkani Sprague-Dawley MeSH
- protonová magnetická rezonanční spektroskopie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Major depressive disorder (MDD) is a mental illness with a high worldwide prevalence and suboptimal pharmacological treatment, which necessitates the development of novel, more efficacious MDD medication. Nuclear magnetic resonance (NMR) can non-invasively provide insight into the neurochemical state of the brain using proton magnetic resonance spectroscopy (1H MRS), and an assessment of regional cerebral blood flow (rCBF) by perfusion imaging. These methods may provide valuable in vivo markers of the pathological processes underlying MDD. METHODS: This study examined the effects of the chronic antidepressant medication, citalopram, in a well-validated MDD model induced by bilateral olfactory bulbectomy (OB) in rats. 1H MRS was utilized to assess key metabolite ratios in the dorsal hippocampus and sensorimotor cortex bilaterally, and arterial spin labelling was employed to estimate rCBF in several additional brain regions. RESULTS: The 1H MRS data results suggest lower hippocampal Cho/tCr and lower cortical NAA/tCr levels as a characteristic of the OB phenotype. Spectroscopy revealed lower hippocampal Tau/tCr in citalopram-treated rats, indicating a potentially deleterious effect of the drug. However, the significant OB model-citalopram treatment interaction was observed using 1H MRS in hippocampal mI/tCr, Glx/tCr and Gln/tCr, indicating differential treatment effects in the OB and control groups. The perfusion data revealed higher rCBF in the whole brain, hippocampus and thalamus in the OB rats, while citalopram appeared to normalise it without affecting the control group. CONCLUSION: Collectively, 1H MRS and rCBF approaches demonstrated their capacity to capture an OB-induced phenotype and chronic antidepressant treatment effect in multiple brain regions.
Department of Condensed Matter Physics Faculty of Science Masaryk University Brno Czech Republic
Department of Pharmacology Faculty of Medicine Masaryk University Brno Czech Republic
Institute of Scientific Instruments of the Czech Academy of Sciences Brno Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25003182
- 003
- CZ-PrNML
- 005
- 20250206104104.0
- 007
- ta
- 008
- 250121e20241101fr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.biopha.2024.117656 $2 doi
- 035 __
- $a (PubMed)39486369
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a fr
- 100 1_
- $a Harastova-Pavlova, Iveta $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic; Department of Condensed Matter Physics, Faculty of Science, Masaryk University, Brno, Czech Republic
- 245 10
- $a Chronic citalopram effects on the brain neurochemical profile and perfusion in a rat model of depression detected by the NMR techniques - spectroscopy and perfusion / $c I. Harastova-Pavlova, E. Drazanova, L. Kratka, P. Amchova, M. Hrickova, O. Macicek, J. Vitous, R. Jirik, J. Ruda-Kucerova
- 520 9_
- $a BACKGROUND: Major depressive disorder (MDD) is a mental illness with a high worldwide prevalence and suboptimal pharmacological treatment, which necessitates the development of novel, more efficacious MDD medication. Nuclear magnetic resonance (NMR) can non-invasively provide insight into the neurochemical state of the brain using proton magnetic resonance spectroscopy (1H MRS), and an assessment of regional cerebral blood flow (rCBF) by perfusion imaging. These methods may provide valuable in vivo markers of the pathological processes underlying MDD. METHODS: This study examined the effects of the chronic antidepressant medication, citalopram, in a well-validated MDD model induced by bilateral olfactory bulbectomy (OB) in rats. 1H MRS was utilized to assess key metabolite ratios in the dorsal hippocampus and sensorimotor cortex bilaterally, and arterial spin labelling was employed to estimate rCBF in several additional brain regions. RESULTS: The 1H MRS data results suggest lower hippocampal Cho/tCr and lower cortical NAA/tCr levels as a characteristic of the OB phenotype. Spectroscopy revealed lower hippocampal Tau/tCr in citalopram-treated rats, indicating a potentially deleterious effect of the drug. However, the significant OB model-citalopram treatment interaction was observed using 1H MRS in hippocampal mI/tCr, Glx/tCr and Gln/tCr, indicating differential treatment effects in the OB and control groups. The perfusion data revealed higher rCBF in the whole brain, hippocampus and thalamus in the OB rats, while citalopram appeared to normalise it without affecting the control group. CONCLUSION: Collectively, 1H MRS and rCBF approaches demonstrated their capacity to capture an OB-induced phenotype and chronic antidepressant treatment effect in multiple brain regions.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a citalopram $x farmakologie $7 D015283
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 12
- $a modely nemocí na zvířatech $7 D004195
- 650 12
- $a mozek $x metabolismus $x účinky léků $7 D001921
- 650 12
- $a mozkový krevní oběh $x účinky léků $7 D002560
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Sprague-Dawley $7 D017207
- 650 _2
- $a magnetická rezonanční spektroskopie $x metody $7 D009682
- 650 _2
- $a deprese $x farmakoterapie $x metabolismus $7 D003863
- 650 _2
- $a hipokampus $x metabolismus $x účinky léků $7 D006624
- 650 _2
- $a protonová magnetická rezonanční spektroskopie $7 D066244
- 650 _2
- $a depresivní porucha unipolární $x farmakoterapie $x metabolismus $7 D003865
- 650 _2
- $a bulbus olfactorius $x metabolismus $x chirurgie $x účinky léků $7 D009830
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Drazanova, Eva $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic; Department of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Kratka, Lucie $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic
- 700 1_
- $a Amchova, Petra $u Department of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Hrickova, Maria $u Department of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- 700 1_
- $a Macicek, Ondrej $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic
- 700 1_
- $a Vitous, Jiri $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic; Department of Biomedical Engineering, Faculty of Electrical Engineering and Communication, Brno University of Technology, Brno, Czech Republic
- 700 1_
- $a Jirik, Radovan $u Institute of Scientific Instruments of the Czech Academy of Sciences, Brno, Czech Republic
- 700 1_
- $a Ruda-Kucerova, Jana $u Department of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic. Electronic address: jkucer@med.muni.cz
- 773 0_
- $w MED00005486 $t Biomedicine & pharmacotherapy $x 1950-6007 $g Roč. 181 (20241101), s. 117656
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39486369 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250121 $b ABA008
- 991 __
- $a 20250206104100 $b ABA008
- 999 __
- $a ok $b bmc $g 2263121 $s 1239189
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 181 $c - $d 117656 $e 20241101 $i 1950-6007 $m Biomedicine & pharmacotherapy $n Biomed Pharmacother $x MED00005486
- LZP __
- $a Pubmed-20250121