Drug intelligence / Profile preview

valproic acid + corticosteroids

Development stage
Unknown
Modality
Small Molecules
Administration
Oral, Intravenous, Intramuscular, Rectal, Topical, Inhalation
01

Overview

This is a combination of valproic acid, an anticonvulsant and mood stabilizer, and corticosteroids, a class of steroid hormones with potent anti-inflammatory and immunosuppressive properties. Valproic acid increases GABAergic neurotransmission in the brain by inhibiting GABA transaminase and succinic semialdehyde dehydrogenase, suppresses voltage-gated sodium channels, and modulates signaling pathways involved in neuroplasticity. It is primarily used to treat epilepsy (various seizure types), bipolar disorder (mania), and for migraine prophylaxis[1][2][5]. Corticosteroids such as prednisone or betamethasone act via glucocorticoid receptors to regulate gene expression, leading to reduced inflammation and immune response[9]. The combination may be considered in clinical scenarios where both neurological stabilization (e.g., seizure control or mood stabilization) and immunosuppression/anti-inflammation are required. There is some evidence for using valproic acid alongside corticosteroids to manage psychiatric side effects induced by steroids without discontinuing steroid therapy[6][7].

02

Targets

ABAT (4-aminobutyrate aminotransferase)GR (Glucocorticoid receptor)HDAC (HDAC family)SSADH (Succinate-semialdehyde dehydrogenase)UGT1A9 (UDP-glucuronosyltransferase 1A9)UGT2B15 (UDP-glucuronosyltransferase 2B15)UGT2B7 (UDP-glucuronosyltransferase 2B7)NaV (Voltage-gated sodium channels)

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