Interneuron Transplantation to Treat Refractory Epilepsy in a California Sea Lion (Zalophus californianus)
IAAAM 2021

Claire A. Simeone1,2; Shawn P. Johnson1*; Mariana Casalia3; John Andrews3; Eric Calvo2; Dianne Cameron2; Edward Chang3; Sophie Dennison4; Ben Inglis5; Kelly Goulet2; Ashley Griffin-Stence2; Ryan Kochanski3; Laura Krasovec6; Kris Kruse-Elliott7; Erin Kuiper2; F. Fabian Okonski8; Dawn Robles2; Gregory Scott2; Scott C. Baraban3

1Sea Change Health, Kentfield, CA, USA; 2Six Flags Discovery Kingdom, Vallejo, CA, USA; 3Department of Neurological Surgery and Weill Institute for Neuroscience, University of California San Francisco, San Francisco, CA, USA; 4TeleVet Imaging Solutions, PLLC, Oakton, VA, USA; 5Wheeler LABS and Henry H. Wheeler Jr. Brain Imaging Center, University of California, Berkeley, CA, USA; 6BrainLab Image-Guided Surgery, Westchester, IL, USA; 7Sage Veterinary Centers, Redwood City, CA, USA; 8Anesthesiology, Perioperative and Pain Medicine, Lucile Packard Children’s Hospital at Stanford, Stanford School of Medicine, Stanford, CA, USA

Abstract

A 7-year-old, stranded, male California sea lion with epilepsy due to left hippocampal atrophy likely caused by domoic acid toxicosis was deemed non-releasable. Over the previous 2 years, he became refractory to antiepileptic drugs (phenobarbital 1.6 mg/kg SID and diazepam 0.05 mg/kg BID) and developed life-threatening periods of anorexia. Eight convulsive seizures were observed in the 2 weeks prior to surgery. A novel interneuron-based cell transplantation using GABA progenitor cells from porcine embryonic medial ganglionic eminence (MGE) was performed with the goal to eliminate seizures and improve “quality of life” measures.1,2 Porcine MGE progenitor cells (50,000 cells/site) were surgically transplanted into four locations in the damaged hippocampus and entorhinal cortex. Sea lion MRI and CT imaging data were used to guide the stereotaxic surgical procedure. Immunosuppressive doses of cyclosporine (3 mg/kg BID) and dexamethasone (0.17 mg/kg SID) were given pre- and post-transplantation. At 60 days post-transplant, no seizures nor neurological deficits have been observed, and the sea lion’s appetite and weight are stable. Over the next 4 months, the immunosuppressive drug regimen will be tapered down. In addition, based on observed seizure activity and behaviors, antiepileptic drugs will be slowly withdrawn. This novel surgical procedure case study demonstrates the potential to successfully xenotransplant porcine MGE interneurons into sea lions for potential resolution of refractory epilepsy.

Acknowledgements

The authors wish to thank the sea lion training staff at Six Flags Discovery Kingdom for the care and training of the sea lion and the staff at SAGE Veterinary Centers for providing imaging and surgical support.

*Presenting author

Literature Cited

1.  Casalia ML, Li T, Ramsay H, Ross PJ, Paredes MF, Baraban SC. 2020. Pallial interneuron origins in the embryonic porcine medial ganglionic eminence. J Neurosci. Provisionally accepted.

2.  Hunt RF, Girskis KM, Rubenstein JL, Alvarez-Buylla A, Baraban SC. 2013. GABA progenitors grafted into the adult epileptic brain control seizures and abnormal behavior. Nat Neurosci. 16:692–697.

 

Speaker Information
(click the speaker's name to view other papers and abstracts submitted by this speaker)

Shawn Johnson
Sea Change Health
Kentfield, CA, USA


MAIN : Session 8: Case Presentations 1 : Refractory Epilepsy & Interneuron Transplantation
Powered By VIN
SAID=27