GABAergic and glutamatergic inputs to the medulla oblongata and locus coeruleus noradrenergic pathways are critical for seizures and postictal antinociception neuromodulation

Sci Rep. 2024 Feb 19;14(1):4069. doi: 10.1038/s41598-024-53744-3.

Abstract

We investigated the participation of the nucleus of the tractus solitarius (NTS) in tonic‒clonic seizures and postictal antinociception control mediated by NMDA receptors, the role of NTS GABAergic interneurons and noradrenergic pathways from the locus coeruleus (LC) in these phenomena. The NTS-lateral nucleus reticularis paragigantocellularis (lPGi)-LC pathway was studied by evaluating neural tract tracer deposits in the lPGi. NMDA and GABAergic receptors agonists and antagonists were microinjected into the NTS, followed by pharmacologically induced seizures. The effects of LC neurotoxic lesions caused by DSP-4, followed by NTS-NMDA receptor activation, on both tonic‒clonic seizures and postictal antinociception were also investigated. The NTS is connected to lPGi neurons that send outputs to the LC. Glutamatergic vesicles were found on dendrites and perikarya of GABAergic interneurons in the NTS. Both tonic‒clonic seizures and postictal antinociception are partially dependent on glutamatergic-mediated neurotransmission in the NTS of seizing rats in addition to the integrity of the noradrenergic system since NMDA receptor blockade in the NTS and intrathecal administration of DSP-4 decrease the postictal antinociception. The GABAA receptor activation in the NTS decreases both seizure severity and postictal antinociception. These findings suggest that glutamatergic inputs to NTS-GABAergic interneurons, in addition to ascending and descending noradrenergic pathways from the LC, are critical for the control of both seizures and postictal antinociception.

Keywords: GABAA receptor; Locus coeruleus; NMDA receptor; Noradrenergic pathways; Nucleus of the tractus solitarius; Refractory epilepsy; Tonic‒clonic seizures.

MeSH terms

  • Animals
  • Benzylamines*
  • Locus Coeruleus* / physiology
  • Medulla Oblongata / metabolism
  • Norepinephrine / metabolism
  • Rats
  • Receptors, N-Methyl-D-Aspartate* / metabolism
  • Seizures / metabolism
  • Solitary Nucleus / metabolism

Substances

  • DSP 4
  • Receptors, N-Methyl-D-Aspartate
  • Norepinephrine
  • Benzylamines