The Experts below are selected from a list of 9 Experts worldwide ranked by ideXlab platform
Luca Pani - One of the best experts on this subject based on the ideXlab platform.
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Carmoxirole is able to reduce amisulpride-induced hyperProlactinemia without affecting its central effect.
European journal of pharmacology, 2002Co-Authors: Giorgio Marchese, Stefania Ruiu, Paola Casti, Francesco Bartholini, Pierluigi Saba, Gian Luigi Gessa, Luca PaniAbstract:Abstract Prolactin Blood Level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D 2 receptor agonists with high or low propensity to cross the brain–Blood barrier, respectively. Administration of amisulpride produced a maximum increase in rat serum Prolactin Level (315±18%) vs. vehicle-treated animals (ED 50 =0.25±0.017 mg/kg, s.c.). The concurrent administration of carmoxirole or bromocriptine completely reversed the hyperProlactinemia induced by amisulpride (0.5 mg/kg, s.c.) (ID 50 =14.9±0.8 mg/kg and 0.81±0.03 mg/kg, respectively). Carmoxirole (15 mg/kg, i.p.) did not affect yawning induced by apomorphine (0.08 mg/kg, s.c.) nor amisulpride (0.5 mg/kg, s.c.) blockade of apomorphine-induced yawning. Conversely, a significant increase in the number of yawns was observed when bromocriptine (0.8 mg/kg, i.p.) was associated with apomorphine in the absence or presence of amisulpride. These results suggested that a peripheral dopamine D 2 receptor agonists could be a useful tool in alleviating amisulpride-induced hyperProlactinemia without possibly affecting its central effect.
Giorgio Marchese - One of the best experts on this subject based on the ideXlab platform.
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Carmoxirole is able to reduce amisulpride-induced hyperProlactinemia without affecting its central effect.
European journal of pharmacology, 2002Co-Authors: Giorgio Marchese, Stefania Ruiu, Paola Casti, Francesco Bartholini, Pierluigi Saba, Gian Luigi Gessa, Luca PaniAbstract:Abstract Prolactin Blood Level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D 2 receptor agonists with high or low propensity to cross the brain–Blood barrier, respectively. Administration of amisulpride produced a maximum increase in rat serum Prolactin Level (315±18%) vs. vehicle-treated animals (ED 50 =0.25±0.017 mg/kg, s.c.). The concurrent administration of carmoxirole or bromocriptine completely reversed the hyperProlactinemia induced by amisulpride (0.5 mg/kg, s.c.) (ID 50 =14.9±0.8 mg/kg and 0.81±0.03 mg/kg, respectively). Carmoxirole (15 mg/kg, i.p.) did not affect yawning induced by apomorphine (0.08 mg/kg, s.c.) nor amisulpride (0.5 mg/kg, s.c.) blockade of apomorphine-induced yawning. Conversely, a significant increase in the number of yawns was observed when bromocriptine (0.8 mg/kg, i.p.) was associated with apomorphine in the absence or presence of amisulpride. These results suggested that a peripheral dopamine D 2 receptor agonists could be a useful tool in alleviating amisulpride-induced hyperProlactinemia without possibly affecting its central effect.
Stefania Ruiu - One of the best experts on this subject based on the ideXlab platform.
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Carmoxirole is able to reduce amisulpride-induced hyperProlactinemia without affecting its central effect.
European journal of pharmacology, 2002Co-Authors: Giorgio Marchese, Stefania Ruiu, Paola Casti, Francesco Bartholini, Pierluigi Saba, Gian Luigi Gessa, Luca PaniAbstract:Abstract Prolactin Blood Level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D 2 receptor agonists with high or low propensity to cross the brain–Blood barrier, respectively. Administration of amisulpride produced a maximum increase in rat serum Prolactin Level (315±18%) vs. vehicle-treated animals (ED 50 =0.25±0.017 mg/kg, s.c.). The concurrent administration of carmoxirole or bromocriptine completely reversed the hyperProlactinemia induced by amisulpride (0.5 mg/kg, s.c.) (ID 50 =14.9±0.8 mg/kg and 0.81±0.03 mg/kg, respectively). Carmoxirole (15 mg/kg, i.p.) did not affect yawning induced by apomorphine (0.08 mg/kg, s.c.) nor amisulpride (0.5 mg/kg, s.c.) blockade of apomorphine-induced yawning. Conversely, a significant increase in the number of yawns was observed when bromocriptine (0.8 mg/kg, i.p.) was associated with apomorphine in the absence or presence of amisulpride. These results suggested that a peripheral dopamine D 2 receptor agonists could be a useful tool in alleviating amisulpride-induced hyperProlactinemia without possibly affecting its central effect.
Paola Casti - One of the best experts on this subject based on the ideXlab platform.
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Carmoxirole is able to reduce amisulpride-induced hyperProlactinemia without affecting its central effect.
European journal of pharmacology, 2002Co-Authors: Giorgio Marchese, Stefania Ruiu, Paola Casti, Francesco Bartholini, Pierluigi Saba, Gian Luigi Gessa, Luca PaniAbstract:Abstract Prolactin Blood Level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D 2 receptor agonists with high or low propensity to cross the brain–Blood barrier, respectively. Administration of amisulpride produced a maximum increase in rat serum Prolactin Level (315±18%) vs. vehicle-treated animals (ED 50 =0.25±0.017 mg/kg, s.c.). The concurrent administration of carmoxirole or bromocriptine completely reversed the hyperProlactinemia induced by amisulpride (0.5 mg/kg, s.c.) (ID 50 =14.9±0.8 mg/kg and 0.81±0.03 mg/kg, respectively). Carmoxirole (15 mg/kg, i.p.) did not affect yawning induced by apomorphine (0.08 mg/kg, s.c.) nor amisulpride (0.5 mg/kg, s.c.) blockade of apomorphine-induced yawning. Conversely, a significant increase in the number of yawns was observed when bromocriptine (0.8 mg/kg, i.p.) was associated with apomorphine in the absence or presence of amisulpride. These results suggested that a peripheral dopamine D 2 receptor agonists could be a useful tool in alleviating amisulpride-induced hyperProlactinemia without possibly affecting its central effect.
Francesco Bartholini - One of the best experts on this subject based on the ideXlab platform.
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Carmoxirole is able to reduce amisulpride-induced hyperProlactinemia without affecting its central effect.
European journal of pharmacology, 2002Co-Authors: Giorgio Marchese, Stefania Ruiu, Paola Casti, Francesco Bartholini, Pierluigi Saba, Gian Luigi Gessa, Luca PaniAbstract:Abstract Prolactin Blood Level and apomorphine-induced yawning were studied in rats treated with the substituted benzamide amisulpride in association with bromocriptine or carmoxirole; two dopamine D 2 receptor agonists with high or low propensity to cross the brain–Blood barrier, respectively. Administration of amisulpride produced a maximum increase in rat serum Prolactin Level (315±18%) vs. vehicle-treated animals (ED 50 =0.25±0.017 mg/kg, s.c.). The concurrent administration of carmoxirole or bromocriptine completely reversed the hyperProlactinemia induced by amisulpride (0.5 mg/kg, s.c.) (ID 50 =14.9±0.8 mg/kg and 0.81±0.03 mg/kg, respectively). Carmoxirole (15 mg/kg, i.p.) did not affect yawning induced by apomorphine (0.08 mg/kg, s.c.) nor amisulpride (0.5 mg/kg, s.c.) blockade of apomorphine-induced yawning. Conversely, a significant increase in the number of yawns was observed when bromocriptine (0.8 mg/kg, i.p.) was associated with apomorphine in the absence or presence of amisulpride. These results suggested that a peripheral dopamine D 2 receptor agonists could be a useful tool in alleviating amisulpride-induced hyperProlactinemia without possibly affecting its central effect.
