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  • 1
    ISSN: 0196-9781
    Keywords: Behavioral effects ; Chronic treatment ; MIF-1 ; Neonatal handling
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0196-9781
    Keywords: EEG ; Learning ; MIF-1 ; Ontogeny ; Prolyl-leucyl-glycinamide (PLG) ; Reflexes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1041
    Keywords: Migraine ; nimodipine ; propranolol ; prolactin ; luteinizing hormone ; growth hormone ; adverse effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Serum prolactin is increased during chronic flunarizine treatment of patients suffering from migraine. In order to clarify the role of calcium in control of the secretion of anterior pituitary hormones, a study has now been made of the effects of chronic nimodipine and propranolol treatment of migraine patients on prolactin (PRL), luteinizing hormone (LH) and growth hormone (GH) levels. 11 patients were treated with nimodipine and 8 with propranolol for four months. A statistically significant reduction in the frequency of the attacks was demonstrated in both groups. No significant change was found in the hormones levels during nimodipine treatment.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Maternal behaviour ; Pup-related stimuli ; Prenatal oxazepam ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract There is evidence that activity at the GABA/benzodiazepine receptor complex in specific brain areas might be enhanced during rodent motherhood. We tested the hypothesis that the manipulation of this neurochemical system by prenatal benzodiazepine exposure affects typical behavioural responses of lactating mouse dams. Outbred CD-1 mouse fetuses were administered either oxazepam (OX, 15 mg/kg) or vehicle twice a day on embryonic days 12–16 and fostered at birth to untreated dams. Female offspring were subsequently mated at the young adult stage. In a first experiment, the behavioural repertoire of the two groups of lactating females was scored (single 10-min session) from postpartum days 3 to 18. When compared with VEH dams, OX females showed a shorter duration ofpup-sniffing at 7–10 days and enhancedcrouching behaviour when pups had reached the age of 14–18 days. In addition, OX-treated dams used more cotton for nest construction than the controls. The two female groups were differentiated only in the presence of their offspring. In a second experiment aimed at investigating possible OX-induced changes in pup-stimulus perception, the same lactating females were challenged in sequence on postpartum day 8 with three different patterns of pup-related cues consisting of: three 8-day-old live male pups (LP), three same-age dead pups DP, or three dead pups accompanied by pre-recorded ultrasounds (DPU). In the absence of carry-over effects of prenatal dam treatment, LP stimuli elicited a higher frequency ofsniffing anddigging than the others, whereas the level oflicking, andgrooming was reduced. In conclusion, the present results indicate that the slight alteration in maternal care resulting from prenatal OX treatment can be dissociated from changes in pup-related stimulus perception.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-2665
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract During detailed visual function testing, pattern-reversal visual evoked potentials (VEP), generated by different spatial frequencies (3c/d, 1c/d and 0.6c/d) and visual contrasts (100% and 10%) were recorded in 21 adolescent and young adult phenylketonuric (PKU) patients (11 females and 10 males; mean age 14.8 years, range 9–22.8) on and off diet. In 14 of the 21 patients, disease had been detected at neonatal screening and in 7 later. Ten age-matched healthy subjects acted as controls. Recordings in more than 40% of eyes in the whole group and 30% of eyes in the screening subgroup showed a prolonged P100 latency. All visual pattern stimuli elicited a significantly longer P100 latency in PKU patients than in controls. VEP latencies to 3c/d, 1c/d and 1c/d with 10% contrast – but not to 0.6c/d – were longer in patients off diet than in patients on diet. No differences were found between VEP latencies in early- and later-detected subjects. To study the link between biochemical variables and VEP latencies, we envisaged either a linear relationship between recent exposure to phenylalanine (Phe) and VEP abnormalities or a threshold model considering phenylalanine (Phe) concentrations among the factors influencing VEP latencies. The correlation analysis detected an association between plasma Phe concentrations and abnormal VEP latencies, predicting that plasma Phe concentrations 〉901 μmol/L would prolong VEP latencies to 1c/d; concentrations 〉879 μmol/L would prolong latencies to 3c/d; and concentrations 〉898 μmol/L would prolong latencies to 1c/d with 10% contrast. Finally, our data confirmed a lack of correlation between white-matter abnormalities on MRI and abnormal VEP latencies. Our findings suggest that in young patients with PKU, prolonged, late exposure to high plasma Phe concentrations induces subclinical visual dysfunction. Although our findings do not allow us to specify the origin of visual system changes in PKU, they favour impairment of the retinal loop as the responsible mechanism.
    Type of Medium: Electronic Resource
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