-
Something wrong with this record ?
How various drugs affect anxiety-related behavior in male and female rats prenatally exposed to methamphetamine
E. Macúchová, M. Ševčíková, I. Hrebíčková, K. Nohejlová, R. Šlamberová,
Language English Country England, Great Britain
Document type Journal Article
Grant support
NT14484
MZ0
CEP Register
- MeSH
- Analgesics pharmacology MeSH
- Analysis of Variance MeSH
- Maze Learning drug effects MeSH
- Time Factors MeSH
- Estrous Cycle drug effects MeSH
- Rats MeSH
- Methamphetamine toxicity MeSH
- N-Methyl-3,4-methylenedioxyamphetamine pharmacology MeSH
- Exploratory Behavior drug effects MeSH
- Serotonin Agents pharmacology MeSH
- Sex Factors MeSH
- Central Nervous System Stimulants toxicity MeSH
- Pregnancy MeSH
- Anxiety chemically induced MeSH
- Prenatal Exposure Delayed Effects chemically induced physiopathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Different forms of anxiety-related behavior have been reported after a single drug use of many abused substances, however, less is known about how males and females are affected differently from exposure to various drugs. Furthermore, chronic prenatal methamphetamine (MA) exposure was shown to predispose the animal to an increased sensitivity to drugs administrated in adulthood. Using the Elevated plus-maze test (EPM), the first aim of the present study was to examine how male and female rats are affected by acute drug treatment with subcutaneously (s.c.) administrated (a) MA (1mg/kg); (b) drugs with a similar mechanism of action to MA: amphetamine (AMP, 1mg/kg), cocaine (COC, 5mg/kg), 3,4-methylenedioxymethamphetamine (MDMA, 5mg/kg); and (c) drugs with different mechanisms of action: morphine (MOR, 5mg/kg), and Δ 9-tetrahydrocannabinol (THC, 2mg/kg). The second aim was to determine if prenatally MA-exposed (5mg/kg) animals show an increased sensitivity to adult drug treatment. The parameters analyzed were divided into two categories: anxiety-related behavior and anxiety-unrelated/exploratory behavior. Our results showed in female rats a decreased percentage of the time spent in the closed arms (CA) after MA, and an increased percentage of the time spent in the open arms (OA) after MA, AMP, and COC treatment, indicating an anxiolytic-like effect. In females, MDMA and THC treatment increased the percentage of the time spent in the CA. An increased percentage of the time spent in the CA was also seen after MOR treatment in females as well as in males, indicating an anxiogenic-like effect. As far as the interaction between prenatal MA exposure and adult drug treatment is concerned, there was no effect found. In conclusion, it seems that: (a) in some cases female rats are more vulnerable to acute drug treatment, in terms of either anxiogenic- or anxiolytic-like effects; (b) prenatal MA exposure does not sensitize animals to the anxiety-related effects of any of the drugs.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17013958
- 003
- CZ-PrNML
- 005
- 20181030120555.0
- 007
- ta
- 008
- 170413s2016 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.ijdevneu.2016.04.001 $2 doi
- 035 __
- $a (PubMed)27067624
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Macúchová, Eva $u Charles University in Prague, Third Faculty of Medicine, Department of Normal, Pathological and Clinical Physiology, Prague, Czech Republic. $7 xx0235047
- 245 10
- $a How various drugs affect anxiety-related behavior in male and female rats prenatally exposed to methamphetamine / $c E. Macúchová, M. Ševčíková, I. Hrebíčková, K. Nohejlová, R. Šlamberová,
- 520 9_
- $a Different forms of anxiety-related behavior have been reported after a single drug use of many abused substances, however, less is known about how males and females are affected differently from exposure to various drugs. Furthermore, chronic prenatal methamphetamine (MA) exposure was shown to predispose the animal to an increased sensitivity to drugs administrated in adulthood. Using the Elevated plus-maze test (EPM), the first aim of the present study was to examine how male and female rats are affected by acute drug treatment with subcutaneously (s.c.) administrated (a) MA (1mg/kg); (b) drugs with a similar mechanism of action to MA: amphetamine (AMP, 1mg/kg), cocaine (COC, 5mg/kg), 3,4-methylenedioxymethamphetamine (MDMA, 5mg/kg); and (c) drugs with different mechanisms of action: morphine (MOR, 5mg/kg), and Δ 9-tetrahydrocannabinol (THC, 2mg/kg). The second aim was to determine if prenatally MA-exposed (5mg/kg) animals show an increased sensitivity to adult drug treatment. The parameters analyzed were divided into two categories: anxiety-related behavior and anxiety-unrelated/exploratory behavior. Our results showed in female rats a decreased percentage of the time spent in the closed arms (CA) after MA, and an increased percentage of the time spent in the open arms (OA) after MA, AMP, and COC treatment, indicating an anxiolytic-like effect. In females, MDMA and THC treatment increased the percentage of the time spent in the CA. An increased percentage of the time spent in the CA was also seen after MOR treatment in females as well as in males, indicating an anxiogenic-like effect. As far as the interaction between prenatal MA exposure and adult drug treatment is concerned, there was no effect found. In conclusion, it seems that: (a) in some cases female rats are more vulnerable to acute drug treatment, in terms of either anxiogenic- or anxiolytic-like effects; (b) prenatal MA exposure does not sensitize animals to the anxiety-related effects of any of the drugs.
- 650 _2
- $a analgetika $x farmakologie $7 D000700
- 650 _2
- $a analýza rozptylu $7 D000704
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a úzkost $x chemicky indukované $7 D001007
- 650 _2
- $a stimulanty centrálního nervového systému $x toxicita $7 D000697
- 650 _2
- $a estrální cyklus $x účinky léků $7 D030762
- 650 _2
- $a pátrací chování $x účinky léků $7 D005106
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a bludiště - učení $x účinky léků $7 D018782
- 650 _2
- $a methamfetamin $x toxicita $7 D008694
- 650 _2
- $a N-methyl-3,4-methylendioxyamfetamin $x farmakologie $7 D018817
- 650 _2
- $a těhotenství $7 D011247
- 650 _2
- $a zpožděný efekt prenatální expozice $x chemicky indukované $x patofyziologie $7 D011297
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a serotoninové látky $x farmakologie $7 D018490
- 650 _2
- $a sexuální faktory $7 D012737
- 650 _2
- $a časové faktory $7 D013997
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Ševčíková, Mária $u Charles University in Prague, Third Faculty of Medicine, Department of Normal, Pathological and Clinical Physiology, Prague, Czech Republic. $7 xx0214442
- 700 1_
- $a Hřebíčková, Ivana $u Charles University in Prague, Third Faculty of Medicine, Department of Normal, Pathological and Clinical Physiology, Prague, Czech Republic. $7 xx0280681
- 700 1_
- $a Nohejlová, Kateryna $u Charles University in Prague, Third Faculty of Medicine, Department of Normal, Pathological and Clinical Physiology, Prague, Czech Republic. $7 mzk2013788463
- 700 1_
- $a Šlamberová, Romana $u Charles University in Prague, Third Faculty of Medicine, Department of Normal, Pathological and Clinical Physiology, Prague, Czech Republic. Electronic address: romana.slamberova@lf3.cuni.cz. $7 xx0052834
- 773 0_
- $w MED00002312 $t International journal of developmental neuroscience the official journal of the International Society for Developmental Neuroscience $x 1873-474X $g Roč. 51, č. - (2016), s. 1-11
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/27067624 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170413 $b ABA008
- 991 __
- $a 20181030121111 $b ABA008
- 999 __
- $a ok $b bmc $g 1200423 $s 974736
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 51 $c - $d 1-11 $e 20160408 $i 1873-474X $m International journal of developmental neuroscience $n Int J Dev Neurosci $x MED00002312
- GRA __
- $a NT14484 $p MZ0
- LZP __
- $a Pubmed-20170413