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  • 1
    Electronic Resource
    Electronic Resource
    Behavioral effects of selective and nonselective dopamine agonists on young rats after irreversible antagonism of D1 and/or D2 receptors (1993)
    Springer
    Psychopharmacology 111 (1993), S. 225-232 
    Details
    ISSN: 1432-2072
    Keywords: Dopamine (DA) D1 and D2 receptors ; NPA ; Quinpirole ; SKF 38393 ; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) ; Rat pups
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In general, preweanling and adult rats respond similarly when challenged with competitive dopamine (DA) agonists or antagonists. In contrast, results using a noncompetitive antagonist suggest that the D1 and D2 receptor systems of preweanling and adult rats differ in some critical way. To further assess this phenomenon, the behavioral effects of irreversible receptor blockade were assessed across 8 days in NPA (a nonselective DA agonist), quinpirole (a D2 agonist), or SKF 38393 (a D1 agonist) treated 17-day-old rat pups. The irreversible antagonist N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) did not block the locomotor activity and rearing of NPA- or quinpirole-treated rat pups, nor did EEDQ reduce SKF 38393-induced grooming. Moreover, pretreatment with EEDQ appeared to potentiate the normal increases in locomotor activity and rearing produced by NPA, but only when D2 receptors were not protected by a previous injection of sulpiride (a D2 antagonist). Taken together, these results are consistent with the presence of large reserves of D1 and D2 receptors in the preweanling rat pup.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02245528
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Effects of irreversible dopamine receptor inactivation on locomotor activity and grooming in the 17- and 90-day-old rat (1992)
    Springer
    Psychopharmacology 106 (1992), S. 502-510 
    Details
    ISSN: 1432-2072
    Keywords: Ontogeny ; Rat pups ; Locomotor activity ; Grooming ; EEDQ ; DA receptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Ontogenetic differences in the behavioral recovery of R(-)-propylnorapomorphine (NPA) treated rats were assessed following irreversible DA receptor antagonism by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ). In the first two experiments, 17-and 90-day-old rats were given EEDQ (7.5 or 15.0 mg/kg, IP) or vehicle after half the rats were initially treated with the selective DA D-1 and D-2 antagonists SCH 23390 and sulpiride. (The sulpiride/SCH 23390 treatment protects DA receptors from EEDQ-induced inactivation.) NPA's (0.1 or 1.0 mg/kg) effects on locomotor activity and grooming were assessed 1, 2, 4 and 8 days after the EEDQ pretreatment. In a third experiment, the effects of habituating the 17- and 90-day-old rats to the testing chamber were assessed 1, 2 and 4 days after EEDQ pretreatment. In this experiment, some groups received successive treatments of saline or NPA prior to behavioral testing. To assess the possible effects of drug-sensitization other groups received saline on days 1 and 2 and NPA on day 4. In 90-day-old rats, EEDQ eliminated, for up to 4 days, the ability of NPA to enhance locomotor activity and depress grooming. Prior treatment with DA antagonist drugs was sufficient to protect DA receptors from EEDQ-induced inactivation, since these groups exhibited normal behavioral responses after challenge with NPA. In contrast, EEDQ did not eliminate, and may have enhanced, NPA's effects on the locomotor activity and grooming of 17-day-old rat pups. Habituating the rats to the testing chamber decreased the locomotor activity of the mature rats, but not the 17-day-old rat pups. Drug sensitization did affect locomotor activity, but could not account for the behavioral recovery exhibited by the mature rats and pups. These results indicate that the behavioral effects of EEDQ differ dramatically in young rats compared to adults. The neurochemical bases for these ontogenetic differences remain unknown.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02244822
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Ontogenetic effects of EEDQ on amphetamine-induced behaviors of rats: role of presynaptic processes (1994)
    Springer
    Psychopharmacology 116 (1994), S. 152-160 
    Details
    ISSN: 1432-2072
    Keywords: EEDQ ; Dopamine ; Amphetamine ; Ontogeny ; Rat pups
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Previous research has shown that the alkylating agentN-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline (EEDQ) affects dopamine (DA) synthesis and metabolism in both preweanling and adult rats. In the present study, we attempted to determine the behavioral relevance of EEDQ's presynaptic actions. To that end, 17- and 90-day-old rats were injected with either EEDQ (7.5 mg/kg, IP) or its vehicle 30 min after half the rats were pretreated with the selective DA antagonists SCH 23390 and sulpiride. (SCH 23390/sulpiride pretreatment was used to protect D1 and D2 receptors from EEDQ-induced inactivation.) The behavioral effects of amphetamine (0, 0.1, 0.3, or 1.0 mg/kg, IP) were then assessed 1, 2, 4, and 8 days after EEDQ treatment. Amphetamine-induced behaviors were used to assess EEDQ's presynaptic actions, because amphetamine does not directly bind to the DA receptor, but rather releases DA from the presynaptic terminal. Further, since half of the EEDQ-treated rats had a full complement of DA receptors (i.e., those rats pretreated with SCH 23390/sulpiride), EEDQ's actions in the presynaptic terminal could be dissociated from actions at pre- and postsynaptic receptors. In general, the results showed that EEDQ blocked most of the amphetamine-induced behaviors of both 17- and 90-day-old rats. Surprisingly, pretreatment with SCH 23390 and sulpiride only protected the amphetamine-induced behaviors of adult rats, but not the behaviors of 17-day-old rat pups. When considered together, these results suggest that EEDQ's presynaptic effects are not behaviorally relevant to the adult rat, but may be responsible for eliminating amphetamine-induced behaviors in the 17-day-old rat pup.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02245057
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Ontogeny of behavioral sensitization in the rat: effects of direct and indirect dopamine agonists (1994)
    Springer
    Psychopharmacology 116 (1994), S. 483-490 
    Details
    ISSN: 1432-2072
    Keywords: Behavioral sensitization ; amphetamine ; NPA ; Ontogeny ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In the present study, the abilities of NPA (a direct DA receptor agonist) and amphetamine (an indirect DA receptor agonist) to induce short- and long-term behavioral sensitization were assessed in 11- and 17-day-old rats (age at initial injection). Rats were injected on 4 consecutive days with amphetamine (1.0, 2.5, or 5.0 mg/kg), NPA (1.0 mg/kg), or saline. A final test day occurred either 2 days (experiment 1) or 8 days (experiment 2) later. On the test day, rats given successive agonist injections received a single injection of the same agonist again; whereas rats given successive saline injections received either amphetamine or NPA for the first time. Five minutes after injection, locomotor activity (line-crosses), stereotyped sniffing, and vertical activity were measured during a 30-min testing session. The results showed that 11- and 17-day-old rats exhibited behavioral sensitization when tested with NPA or amphetamine after a 2-day interval. In contrast, neither NPA nor amphetamine was able to sensitize the behaviors of preweanling rats when measured 8 days after initial drug treatments. Therefore, these results show that both direct and indirect DA agonists are able to induce short-term behavioral sensitization in preweanling rats, but that the mechanisms responsible for mediating long-term behavioral sensitization have not yet matured.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02247482
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    Paper (German National Licenses)
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