Detail
Článek
Článek online
FT
Medvik - BMČ
  • 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

. 2021 ; 58 (11) : 5548-5563. [pub] 20210808

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc22012013

Grantová podpora
34119 Grantová Agentura, Univerzita Karlova
Q27/LF1 Univerzita Karlova v Praze

E-zdroje Online Plný text

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

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

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...