-
Je něco špatně v tomto záznamu ?
Effect of Novel Antipsychotics on Energy Metabolism - In Vitro Study in Pig Brain Mitochondria
M. Ľupták, Z. Fišar, J. Hroudová
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
34119
Grantová Agentura, Univerzita Karlova
Q27/LF1
Univerzita Karlova v Praze
NLK
ProQuest Central
od 2019-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2010-02-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2019-01-01 do Před 1 rokem
Psychology Database (ProQuest)
od 2021-01-01 do 2021-12-31
- MeSH
- adenosintrifosfát biosyntéza MeSH
- antipsychotika klasifikace farmakologie MeSH
- chinolony farmakologie MeSH
- elektronový transportní řetězec účinky léků MeSH
- energetický metabolismus účinky léků MeSH
- inhibitory MAO farmakologie MeSH
- loxapin farmakologie MeSH
- lurasidon hydrochlorid farmakologie MeSH
- mitochondrie účinky léků metabolismus MeSH
- peroxid vodíku metabolismus MeSH
- piperaziny farmakologie MeSH
- prasata MeSH
- reaktivní formy kyslíku metabolismus MeSH
- receptory neurotransmiterů účinky léků MeSH
- spotřeba kyslíku účinky léků MeSH
- thiofeny farmakologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The identification and quantification of mitochondrial effects of novel antipsychotics (brexpiprazole, cariprazine, loxapine, and lurasidone) were studied in vitro in pig brain mitochondria. Selected parameters of mitochondrial metabolism, electron transport chain (ETC) complexes, citrate synthase (CS), malate dehydrogenase (MDH), monoamine oxidase (MAO), mitochondrial respiration, and total ATP and reactive oxygen species (ROS) production were evaluated and associated with possible adverse effects of drugs. All tested antipsychotics decreased the ETC activities (except for complex IV, which increased in activity after brexpiprazole and loxapine addition). Both complex I- and complex II-linked respiration were dose-dependently inhibited, and significant correlations were found between complex I-linked respiration and both complex I activity (positive correlation) and complex IV activity (negative correlation). All drugs significantly decreased mitochondrial ATP production at higher concentrations. Hydrogen peroxide production was significantly increased at 10 μM brexpiprazole and lurasidone and at 100 μM cariprazine and loxapine. All antipsychotics acted as partial inhibitors of MAO-A, brexpiprazole and loxapine partially inhibited MAO-B. Based on our results, novel antipsychotics probably lacked oxygen uncoupling properties. The mitochondrial effects of novel antipsychotics might contribute on their adverse effects, which are mostly related to decreased ATP production and increased ROS production, while MAO-A inhibition might contribute to their antidepressant effect, and brexpiprazole- and loxapine-induced MAO-B inhibition might likely promote neuroplasticity and neuroprotection. The assessment of drug-induced mitochondrial dysfunctions is important in development of new drugs as well as in the understanding of molecular mechanism of adverse or side drug effects.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22012013
- 003
- CZ-PrNML
- 005
- 20220506130237.0
- 007
- ta
- 008
- 220425s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12035-021-02498-4 $2 doi
- 035 __
- $a (PubMed)34365585
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Ľupták, Matej $u Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00, Prague 2, Czech Republic. mat.luptak@gmail.com $1 https://orcid.org/0000000180022477
- 245 10
- $a Effect of Novel Antipsychotics on Energy Metabolism - In Vitro Study in Pig Brain Mitochondria / $c M. Ľupták, Z. Fišar, J. Hroudová
- 520 9_
- $a The identification and quantification of mitochondrial effects of novel antipsychotics (brexpiprazole, cariprazine, loxapine, and lurasidone) were studied in vitro in pig brain mitochondria. Selected parameters of mitochondrial metabolism, electron transport chain (ETC) complexes, citrate synthase (CS), malate dehydrogenase (MDH), monoamine oxidase (MAO), mitochondrial respiration, and total ATP and reactive oxygen species (ROS) production were evaluated and associated with possible adverse effects of drugs. All tested antipsychotics decreased the ETC activities (except for complex IV, which increased in activity after brexpiprazole and loxapine addition). Both complex I- and complex II-linked respiration were dose-dependently inhibited, and significant correlations were found between complex I-linked respiration and both complex I activity (positive correlation) and complex IV activity (negative correlation). All drugs significantly decreased mitochondrial ATP production at higher concentrations. Hydrogen peroxide production was significantly increased at 10 μM brexpiprazole and lurasidone and at 100 μM cariprazine and loxapine. All antipsychotics acted as partial inhibitors of MAO-A, brexpiprazole and loxapine partially inhibited MAO-B. Based on our results, novel antipsychotics probably lacked oxygen uncoupling properties. The mitochondrial effects of novel antipsychotics might contribute on their adverse effects, which are mostly related to decreased ATP production and increased ROS production, while MAO-A inhibition might contribute to their antidepressant effect, and brexpiprazole- and loxapine-induced MAO-B inhibition might likely promote neuroplasticity and neuroprotection. The assessment of drug-induced mitochondrial dysfunctions is important in development of new drugs as well as in the understanding of molecular mechanism of adverse or side drug effects.
- 650 _2
- $a adenosintrifosfát $x biosyntéza $7 D000255
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antipsychotika $x klasifikace $x farmakologie $7 D014150
- 650 _2
- $a elektronový transportní řetězec $x účinky léků $7 D045222
- 650 _2
- $a energetický metabolismus $x účinky léků $7 D004734
- 650 _2
- $a peroxid vodíku $x metabolismus $7 D006861
- 650 _2
- $a loxapin $x farmakologie $7 D008152
- 650 _2
- $a lurasidon hydrochlorid $x farmakologie $7 D000069056
- 650 _2
- $a mitochondrie $x účinky léků $x metabolismus $7 D008928
- 650 _2
- $a inhibitory MAO $x farmakologie $7 D008996
- 650 _2
- $a spotřeba kyslíku $x účinky léků $7 D010101
- 650 _2
- $a piperaziny $x farmakologie $7 D010879
- 650 _2
- $a chinolony $x farmakologie $7 D015363
- 650 _2
- $a reaktivní formy kyslíku $x metabolismus $7 D017382
- 650 _2
- $a receptory neurotransmiterů $x účinky léků $7 D017981
- 650 _2
- $a prasata $7 D013552
- 650 _2
- $a thiofeny $x farmakologie $7 D013876
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Fišar, Zdeněk $u Department of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00, Prague 2, Czech Republic
- 700 1_
- $a Hroudová, Jana $u Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00, Prague 2, Czech Republic $u Department of Psychiatry, First Faculty of Medicine, Charles University and General University Hospital in Prague, Ke Karlovu 11, 120 00, Prague 2, Czech Republic
- 773 0_
- $w MED00005280 $t Molecular neurobiology $x 1559-1182 $g Roč. 58, č. 11 (2021), s. 5548-5563
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34365585 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20220506130229 $b ABA008
- 999 __
- $a ok $b bmc $g 1789556 $s 1163214
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 58 $c 11 $d 5548-5563 $e 20210808 $i 1559-1182 $m Molecular neurobiology $n Mol Neurobiol $x MED00005280
- GRA __
- $a 34119 $p Grantová Agentura, Univerzita Karlova
- GRA __
- $a Q27/LF1 $p Univerzita Karlova v Praze
- LZP __
- $a Pubmed-20220425