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Corticosterone 4 pregnen 11b diol 3 20 dione 21 hemisuccinate

Manufactured by Merck Group

Corticosterone (4-pregnen-11b-diol-3 20-dione 21-hemisuccinate) is a laboratory product used for research and analytical purposes. It is a synthetic derivative of the naturally occurring steroid hormone corticosterone. The primary function of this product is to serve as a reference standard or analytical tool in various research and testing applications.

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2 protocols using corticosterone 4 pregnen 11b diol 3 20 dione 21 hemisuccinate

1

Corticosterone-Induced Neuronal Responses

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NSC 23766 (NSC, Tocris) and Fluoxetine (Sigma, St Louis, MO, USA) were administrated intraperitoneally (i.p; 100 μL) at a concentration of 2.5 mg per kg body weight per day (mg kg-1 day-1) and 20 mg kg-1 day-1 respectively. Cysteamine (Sigma) was administrated at a concentration of 150 mg kg-1 day-1 through drinking water for 21 days. corticosterone (4-pregnen-11b-diol-3 20-dione 21-hemisuccinate; Sigma) was dissolved in vehicle (0.45% hydroxypropyl-β-cyclodextrin, Sigma). corticosterone (35 μg/mL, equivalent to 5 mg kg-1 day-1) was delivered ad libitum in the drinking water. The dose and duration of corticosterone treatment in mice were selected based on earlier studies9 (link),25 (link), where the above dose and duration of treatment with CORT induced anxiety and depressive-like behaviors in mice. The fluid intake was monitored throughout the treatment period and the corticosterone dose was adjusted accordingly. Primary cortical neurons were treated with serotonin (5-HT; Sigma) at a concentration of 5-100 μM at DIV 5-7. In glucocorticoid receptor inhibitor studies, cells were treated with RU486 (1 μM; Sigma) 30 min before 48-h corticosterone (1 μM; Sigma) treatment. Neurons were treated with BDNF (prospec) at 100ng/ml for indicated time period.
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2

Corticosterone-Induced Neuronal Responses

Check if the same lab product or an alternative is used in the 5 most similar protocols
NSC 23766 (NSC, Tocris) and Fluoxetine (Sigma, St Louis, MO, USA) were administrated intraperitoneally (i.p; 100 μL) at a concentration of 2.5 mg per kg body weight per day (mg kg-1 day-1) and 20 mg kg-1 day-1 respectively. Cysteamine (Sigma) was administrated at a concentration of 150 mg kg-1 day-1 through drinking water for 21 days. corticosterone (4-pregnen-11b-diol-3 20-dione 21-hemisuccinate; Sigma) was dissolved in vehicle (0.45% hydroxypropyl-β-cyclodextrin, Sigma). corticosterone (35 μg/mL, equivalent to 5 mg kg-1 day-1) was delivered ad libitum in the drinking water. The dose and duration of corticosterone treatment in mice were selected based on earlier studies9 (link),25 (link), where the above dose and duration of treatment with CORT induced anxiety and depressive-like behaviors in mice. The fluid intake was monitored throughout the treatment period and the corticosterone dose was adjusted accordingly. Primary cortical neurons were treated with serotonin (5-HT; Sigma) at a concentration of 5-100 μM at DIV 5-7. In glucocorticoid receptor inhibitor studies, cells were treated with RU486 (1 μM; Sigma) 30 min before 48-h corticosterone (1 μM; Sigma) treatment. Neurons were treated with BDNF (prospec) at 100ng/ml for indicated time period.
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