Allosteric modulation of NMDA receptors prevents the antibody effects of patients with anti-NMDAR encephalitis
| Autor: | James J. Doherty, Xavier Gasull, Marija Radosevic, Estibaliz Maudes, Mike Lewis, Jesús Planagumà, Anna García-Serra, Marta Pedreño, Jing Dai, Francesco Mannara, David Soto, Esther Aguilar, Michael Quirk, Josep Dalmau, Steven M. Paul |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Male
Allosteric modulator Receptors de neurotransmissors Hippocampus Pharmacology Receptors N-Methyl-D-Aspartate Neurotransmitter receptors Mice Organ Culture Techniques Allosteric Regulation Medicine Animals Humans Receptor Phencyclidine Cells Cultured Autoantibodies Anti-N-Methyl-D-Aspartate Receptor Encephalitis business.industry musculoskeletal neural and ocular physiology Antagonist Encefalitis Long-term potentiation Hydroxycholesterols Mice Inbred C57BL HEK293 Cells nervous system Excitatory postsynaptic potential Encephalitis NMDA receptor Neurology (clinical) business medicine.drug |
| Zdroj: | Dipòsit Digital de la UB Universidad de Barcelona |
| ISSN: | 1460-2156 |
| Popis: | Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis is an immune-mediated disease characterized by a complex neuropsychiatric syndrome in association with an antibody-mediated decrease of NMDAR. About 85% of patients respond to immunotherapy (and removal of an associated tumour if it applies), but it often takes several months or more than 1 year for patients to recover. There are no complementary treatments, beyond immunotherapy, to accelerate this recovery. Previous studies showed that SGE-301, a synthetic analogue of 24(S)-hydroxycholesterol, which is a potent and selective positive allosteric modulator of NMDAR, reverted the memory deficit caused by phencyclidine (a non-competitive antagonist of NMDAR), and prevented the NMDAR dysfunction caused by patients’ NMDAR antibodies in cultured neurons. An advantage of SGE-301 is that it is optimized for systemic delivery such that plasma and brain exposures are sufficient to modulate NMDAR activity. Here, we used SGE-301 to confirm that in cultured neurons it prevented the antibody-mediated reduction of receptors, and then we applied it to a previously reported mouse model of passive cerebroventricular transfer of patient’s CSF antibodies. Four groups were established: mice receiving continuous (14-day) infusion of patients’ or controls’ CSF, treated with daily subcutaneous administration of SGE-301 or vehicle (no drug). The effects on memory were examined with the novel object location test at different time points, and the effects on synaptic levels of NMDAR (assessed with confocal microscopy) and plasticity (long-term potentiation) were examined in the hippocampus on Day 18, which in this model corresponds to the last day of maximal clinical and synaptic alterations. As expected, mice infused with patient’s CSF antibodies, but not those infused with controls’ CSF, and treated with vehicle developed severe memory deficit without locomotor alteration, accompanied by a decrease of NMDAR clusters and impairment of long-term potentiation. All antibody-mediated pathogenic effects (memory, synaptic NMDAR, long-term potentiation) were prevented in the animals treated with SGE-301, despite this compound not antagonizing antibody binding. Additional investigations on the potential mechanisms related to these SGE-301 effects showed that (i) in cultured neurons SGE-301 prolonged the decay time of NMDAR-dependent spontaneous excitatory postsynaptic currents suggesting a prolonged open time of the channel; and (ii) it significantly decreased, without fully preventing, the internalization of antibody-bound receptors suggesting that additional, yet unclear mechanisms, contribute in keeping unchanged the surface NMDAR density. Overall, these findings suggest that SGE-301, or similar NMDAR modulators, could potentially serve as complementary treatment for anti-NMDAR encephalitis and deserve future investigations. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|