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Behavioral and antinociceptive effects of different psychostimulant drugs in prenatally methamphetamine-exposed rats
A. Yamamotová, R. Šlamberová
Jazyk angličtina Země Česko
NLK
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- MeSH
- amfetamin farmakologie škodlivé účinky MeSH
- chování zvířat účinky léků MeSH
- kokain farmakokinetika škodlivé účinky MeSH
- krysa rodu rattus MeSH
- methamfetamin farmakologie škodlivé účinky MeSH
- morfin farmakologie škodlivé účinky MeSH
- N-methyl-3,4-methylendioxyamfetamin farmakologie škodlivé účinky MeSH
- narkotika * farmakologie škodlivé účinky MeSH
- stimulanty centrálního nervového systému * farmakologie škodlivé účinky MeSH
- těhotenství MeSH
- zpožděný efekt prenatální expozice * metabolismus patofyziologie psychologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
Prenatal exposure to methamphetamine (METH) increases nociceptive sensitivity in adult rats. As the strong analgesics have high abuse potential and drugs of abuse are known to have analgesic properties, the aim was to study analgesic effect of different psychostimulants in control and prenatally METHexposed rats. Latencies of withdrawal reflexes of hind limbs and the tail on thermal nociceptive stimuli were repeatedly measured in 15-min intervals after the application of 5 mg/kg s.c. of amphetamine (AMPH), methamphetamine (METH), cocaine (COC), 3,4-methylenedioxymethamphetamine (MDMA) or morphine (MOR). In all groups, AMPH induced on hind limbs stronger analgesia than METH and MDMA whereas COC and MOR were practically without any effect. On the tail, effect of AMPH did not differ from that of MOR. All psychostimulants increased defecation in comparison with MOR and in all groups the number of defecation boluses positively correlated with analgesia of the hind limbs. We did not confirm that prenatal exposure to METH makes adult rats more sensitive either to same drug or to other psychostimulants. The different analgesic potencies of psychostimulants and MOR at different body sites indicate the possible existence of a somatotopic organization of pain inhibition, which is controlled by different mechanisms.
Citace poskytuje Crossref.org
Literatura
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