PT  - JOURNAL ARTICLE
AU  - Vuu, Irene
AU  - Patterson, Edward E.
AU  - Wu, Chun-Yi
AU  - Zolkowska, Dorota
AU  - Leppik, Ilo E.
AU  - Rogawski, Michael A.
AU  - Worrell, Gregory A.
AU  - Kremen, Vaclav
AU  - Cloyd, James C.
AU  - Coles, Lisa D.
TI  - Intravenous and Intramuscular Allopregnanolone for Early Treatment of Status Epilepticus: Pharmacokinetics, Pharmacodynamics, and Safety in Dogs
AID  - 10.1124/jpet.121.000736
DP  - 2022 Feb 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 104--113
VI  - 380
IP  - 2
4099  - http://jpet.aspetjournals.org/content/380/2/104.short
4100  - http://jpet.aspetjournals.org/content/380/2/104.full
SO  - J Pharmacol Exp Ther2022 Feb 01; 380
AB  - Allopregnanolone (ALLO) is a neurosteroid that modulates synaptic and extrasynaptic GABAA receptors. We hypothesize that ALLO may be useful as first-line treatment of status epilepticus (SE). Our objectives were to (1) characterize ALLO pharmacokinetics-pharmacodynamics PK-PD after intravenous (IV) and intramuscular (IM) administration and (2) compare IV and IM ALLO safety and tolerability. Three healthy dogs and two with a history of epilepsy were used. Single ALLO IV doses ranging from 1–6 mg/kg were infused over 5 minutes or injected IM. Blood samples, vital signs, and sedation assessment were collected up to 8 hours postdose. Intracranial EEG (iEEG) was continuously recorded in one dog. IV ALLO exhibited dose-proportional increases in exposure, which were associated with an increase in absolute power spectral density in all iEEG frequency bands. This relationship was best described by an indirect link PK-PD model where concentration-response was described by a sigmoidal maximum response (Emax) equation. Adverse events included site injection pain with higher IM volumes and ataxia and sedation associated with higher doses. IM administration exhibited incomplete absorption and volume-dependent bioavailability. Robust iEEG changes after IM administration were not observed. Based on PK-PD simulations, a 2 mg/kg dose infused over 5 minutes is predicted to achieve plasma concentrations above the EC50, but below those associated with heavy sedation. This study demonstrates that ALLO is safe and well tolerated when administered at 1–4 mg/kg IV and up to 2 mg/kg IM. The rapid onset of effect after IV infusion suggests that ALLO may be useful in the early treatment of SE.SIGNIFICANCE STATEMENT The characterization of the pharmacokinetics and pharmacodynamics of allopregnanolone is essential in order to design clinical studies evaluating its effectiveness as an early treatment for status epilepticus in dogs and people. This study has proposed a target dose/therapeutic range for a clinical trial in canine status epilepticus.