Prenatal Exposure to Drugs of Abuse May Affect Later Behavior and Learning

1998 ◽  
Author(s):  
Robert Mathias
Author(s):  
O. Castillo ◽  
I. González ◽  
E. Prieto ◽  
T. Pérez ◽  
I. Altemir ◽  
...  

2012 ◽  
Vol 34 (1) ◽  
pp. 73-79 ◽  
Author(s):  
S. Ortigosa ◽  
B. Friguls ◽  
X. Joya ◽  
S. Martinez ◽  
M.L. Mariñoso ◽  
...  

2018 ◽  
Vol 19 (2) ◽  
pp. 136-143 ◽  
Author(s):  
Laura Cortes ◽  
Laura Almeida ◽  
Sally Sabra ◽  
Marta Muniesa ◽  
Francesco P. Busardo ◽  
...  

Author(s):  
Antonia Roca ◽  
Pilar Jarque ◽  
Isabel Gomila ◽  
Emilia Marchei ◽  
Roberta Tittarelli ◽  
...  

NeuroImage ◽  
2011 ◽  
Vol 54 (4) ◽  
pp. 3067-3075 ◽  
Author(s):  
Florence F. Roussotte ◽  
Jennifer E. Bramen ◽  
S. Christopher Nunez ◽  
Lorna C. Quandt ◽  
Lynne Smith ◽  
...  

2012 ◽  
pp. S139-S147
Author(s):  
A. YAMAMOTOVÁ ◽  
R. ŠLAMBEROVÁ

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 METH-exposed 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.


Author(s):  
C. Uphoff ◽  
C. Nyquist-Battie

Fetal Alcohol Syndrone (FAS) is a syndrome with characteristic abnormalities resulting from prenatal exposure to ethanol. In many children with FAS syndrome gross pathological changes in the heart are seen with septal defects the most prevalent abnormality recorded. Few studies in animal models have been performed on the effects of ethanol on heart development. In our laboratory, it has been observed that prenatal ethanol exposure of Swiss albino mice results in abnormal cardiac muscle ultrastructure when mice were examined at birth and compared to pairfed and normal controls. Fig. 1 is an example of the changes that are seen in the ethanol-exposed animals. These changes include enlarged mitochondria with loss of inner mitochondrial membrane integrity and loss of myofibrils. Morphometric analysis substantiated the presence of these alterations from normal cardiac ultrastructure. The present work was undertaken to determine if the pathological changes seen in the newborn mice prenatally exposed to ethanol could be reversed with age and abstinence.


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