Limits...
Involvement of NMDA receptor complex in the anxiolytic-like effects of chlordiazepoxide in mice.

Poleszak E, Socała K, Szopa A, Wróbel A, Szewczyk B, Kasperek R, Blicharska E, Nowak G, Wlaź P - J Neural Transm (Vienna) (2011)

Bottom Line: In the present study, we demonstrated that low, ineffective doses of N-methyl-D-aspartic acid (NMDA) receptor antagonists [competitive NMDA antagonist, CGP 37849, at 0.312 mg/kg intraperitoneally (i.p.), antagonist of the glycine(B) sites, L-701,324, at 2 mg/kg i.p., partial agonist of glycine(B) sites, D-cycloserine, at 2.5 mg/kg i.p.] administered jointly with an ineffective dose of the benzodiazepine, chlordiazepoxide (CDP, 2.5 mg/kg i.p.), significantly increased the percentage of time spent in the open arms of the elevated plus-maze (index of anxiolytic effect).Furthermore, CDP-induced anxiolytic-like activity (5 mg/kg i.p.) was antagonized by NMDA (75 mg/kg i.p.) and by an agonist of glycine(B) sites of the NMDA receptor complex, D-serine [100 nmol/mouse intracerebroventricularly (i.c.v.)].The present study showed a positive interaction between γ-aminobutyric acid (GABA) and glutamate neurotransmission in the anxiolytic-like activity in the elevated plus-maze test in mice and this activity seems to particularly involve the NMDA receptors.

View Article: PubMed Central - PubMed

Affiliation: Department of Applied Pharmacy, Medical University of Lublin, Chodźki 1, 20-093 Lublin, Poland. ewa.poleszak@umlub.pl

ABSTRACT
In the present study, we demonstrated that low, ineffective doses of N-methyl-D-aspartic acid (NMDA) receptor antagonists [competitive NMDA antagonist, CGP 37849, at 0.312 mg/kg intraperitoneally (i.p.), antagonist of the glycine(B) sites, L-701,324, at 2 mg/kg i.p., partial agonist of glycine(B) sites, D-cycloserine, at 2.5 mg/kg i.p.] administered jointly with an ineffective dose of the benzodiazepine, chlordiazepoxide (CDP, 2.5 mg/kg i.p.), significantly increased the percentage of time spent in the open arms of the elevated plus-maze (index of anxiolytic effect). Furthermore, CDP-induced anxiolytic-like activity (5 mg/kg i.p.) was antagonized by NMDA (75 mg/kg i.p.) and by an agonist of glycine(B) sites of the NMDA receptor complex, D-serine [100 nmol/mouse intracerebroventricularly (i.c.v.)]. The present study showed a positive interaction between γ-aminobutyric acid (GABA) and glutamate neurotransmission in the anxiolytic-like activity in the elevated plus-maze test in mice and this activity seems to particularly involve the NMDA receptors.

Show MeSH

Related in: MedlinePlus

Effect of joint administration of L-701,324 and chlordiazepoxide (CDP) in the elevated plus-maze procedure in mice [the percentage of the time spent in the open arms (a), and the percentage of the open arms entries (b)]. L-701,324 and CDP was administered i.p. 60 min before the test. The values represent the mean ± SEM (n = 8 mice per group) *p < 0.01 versus L-701,324, ^p < 0.01 versus CDP, #p < 0.01 versus control (vehicle-treated group) (Bonferroni’s test)
© Copyright Policy
Related In: Results  -  Collection


getmorefigures.php?uid=PMC3104009&req=5

Fig2: Effect of joint administration of L-701,324 and chlordiazepoxide (CDP) in the elevated plus-maze procedure in mice [the percentage of the time spent in the open arms (a), and the percentage of the open arms entries (b)]. L-701,324 and CDP was administered i.p. 60 min before the test. The values represent the mean ± SEM (n = 8 mice per group) *p < 0.01 versus L-701,324, ^p < 0.01 versus CDP, #p < 0.01 versus control (vehicle-treated group) (Bonferroni’s test)

Mentions: Chlordiazepoxide administered at a dose of 0.5 mg/kg did not alter the percentage of time spent and increased entries into the open arms (Fig. 2). L-701,324 given alone at a dose of 2 mg/kg exhibited no effect in this test (Fig. 2a, b). The joint administration of CDP and L-701,324 (both in ineffective per se doses) significantly increased the percentage of time spent in the open arms (Fig. 2a), but not in the number of entries into open arms (Fig. 2b). A two-way ANOVA demonstrated a significant effect of CDP [F(1, 28) = 7.66, p = 0.0099], a significant effect of L-701,324 [F(1, 28) = 9.65, p < 0.0043] and not quite significant interaction [F(1, 28) = 3.83, p = 0.0603] in the time spent in open arms, while a significant effect of CDP [F(1, 28) = 7.25, p = 0.0118], no effect of L-701,324 [F(1, 28) = 1.09, p = 0.3056] and not quite significant interaction [F(1, 28) = 3.77, p = 0.0622] in the open arm entries.Fig. 2


Involvement of NMDA receptor complex in the anxiolytic-like effects of chlordiazepoxide in mice.

Poleszak E, Socała K, Szopa A, Wróbel A, Szewczyk B, Kasperek R, Blicharska E, Nowak G, Wlaź P - J Neural Transm (Vienna) (2011)

Effect of joint administration of L-701,324 and chlordiazepoxide (CDP) in the elevated plus-maze procedure in mice [the percentage of the time spent in the open arms (a), and the percentage of the open arms entries (b)]. L-701,324 and CDP was administered i.p. 60 min before the test. The values represent the mean ± SEM (n = 8 mice per group) *p < 0.01 versus L-701,324, ^p < 0.01 versus CDP, #p < 0.01 versus control (vehicle-treated group) (Bonferroni’s test)
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC3104009&req=5

Fig2: Effect of joint administration of L-701,324 and chlordiazepoxide (CDP) in the elevated plus-maze procedure in mice [the percentage of the time spent in the open arms (a), and the percentage of the open arms entries (b)]. L-701,324 and CDP was administered i.p. 60 min before the test. The values represent the mean ± SEM (n = 8 mice per group) *p < 0.01 versus L-701,324, ^p < 0.01 versus CDP, #p < 0.01 versus control (vehicle-treated group) (Bonferroni’s test)
Mentions: Chlordiazepoxide administered at a dose of 0.5 mg/kg did not alter the percentage of time spent and increased entries into the open arms (Fig. 2). L-701,324 given alone at a dose of 2 mg/kg exhibited no effect in this test (Fig. 2a, b). The joint administration of CDP and L-701,324 (both in ineffective per se doses) significantly increased the percentage of time spent in the open arms (Fig. 2a), but not in the number of entries into open arms (Fig. 2b). A two-way ANOVA demonstrated a significant effect of CDP [F(1, 28) = 7.66, p = 0.0099], a significant effect of L-701,324 [F(1, 28) = 9.65, p < 0.0043] and not quite significant interaction [F(1, 28) = 3.83, p = 0.0603] in the time spent in open arms, while a significant effect of CDP [F(1, 28) = 7.25, p = 0.0118], no effect of L-701,324 [F(1, 28) = 1.09, p = 0.3056] and not quite significant interaction [F(1, 28) = 3.77, p = 0.0622] in the open arm entries.Fig. 2

Bottom Line: In the present study, we demonstrated that low, ineffective doses of N-methyl-D-aspartic acid (NMDA) receptor antagonists [competitive NMDA antagonist, CGP 37849, at 0.312 mg/kg intraperitoneally (i.p.), antagonist of the glycine(B) sites, L-701,324, at 2 mg/kg i.p., partial agonist of glycine(B) sites, D-cycloserine, at 2.5 mg/kg i.p.] administered jointly with an ineffective dose of the benzodiazepine, chlordiazepoxide (CDP, 2.5 mg/kg i.p.), significantly increased the percentage of time spent in the open arms of the elevated plus-maze (index of anxiolytic effect).Furthermore, CDP-induced anxiolytic-like activity (5 mg/kg i.p.) was antagonized by NMDA (75 mg/kg i.p.) and by an agonist of glycine(B) sites of the NMDA receptor complex, D-serine [100 nmol/mouse intracerebroventricularly (i.c.v.)].The present study showed a positive interaction between γ-aminobutyric acid (GABA) and glutamate neurotransmission in the anxiolytic-like activity in the elevated plus-maze test in mice and this activity seems to particularly involve the NMDA receptors.

View Article: PubMed Central - PubMed

Affiliation: Department of Applied Pharmacy, Medical University of Lublin, Chodźki 1, 20-093 Lublin, Poland. ewa.poleszak@umlub.pl

ABSTRACT
In the present study, we demonstrated that low, ineffective doses of N-methyl-D-aspartic acid (NMDA) receptor antagonists [competitive NMDA antagonist, CGP 37849, at 0.312 mg/kg intraperitoneally (i.p.), antagonist of the glycine(B) sites, L-701,324, at 2 mg/kg i.p., partial agonist of glycine(B) sites, D-cycloserine, at 2.5 mg/kg i.p.] administered jointly with an ineffective dose of the benzodiazepine, chlordiazepoxide (CDP, 2.5 mg/kg i.p.), significantly increased the percentage of time spent in the open arms of the elevated plus-maze (index of anxiolytic effect). Furthermore, CDP-induced anxiolytic-like activity (5 mg/kg i.p.) was antagonized by NMDA (75 mg/kg i.p.) and by an agonist of glycine(B) sites of the NMDA receptor complex, D-serine [100 nmol/mouse intracerebroventricularly (i.c.v.)]. The present study showed a positive interaction between γ-aminobutyric acid (GABA) and glutamate neurotransmission in the anxiolytic-like activity in the elevated plus-maze test in mice and this activity seems to particularly involve the NMDA receptors.

Show MeSH
Related in: MedlinePlus