Related Experiment Video
Updated: Aug 19, 2026

Experimental Models to Study the Neuroprotection of Acidic Postconditioning Against Cerebral Ischemia
Published on: July 31, 2017
[Endogenous anticonvulsant and neuroprotective agents]
1Zakład Endokrynologii Instytutu Farmakologii, Polskiej Akademii Nauk, Kraków. lason@if-pan.krakow.pl
Abstract:
Elucidation of the biochemical basis of neuronal degeneration following seizures, ischemia or hypoglycemia appears to be one of the most urgent problems of contemporary science. Close attention has been devoted to endogenous anticonvulsant and/or neuroprotective agents which help to maintain a neuronal homeostasis under pathological conditions. The list of putative neuroprotectants is very long and includes substances with diverse chemical structures, such as, e.g., adenosine, amino acids (kinurenic acid, taurine), neuropeptides (opioid peptides, thyreoliberine, neuropeptide Y, galanin, VIP/PACAP) and some neurosteroids (allopregnanolone, dehydroepiandrosterone). In recent years great progress has been made in the studies into not only their biosynthesis, metabolism and regulation of release in the nervous tissue, but also molecular and functional characteristics of their receptors. Apart from fast ionic effects leading to repolarization of the neuronal membrane, these endogenous neuroprotective agents may exert long-term effects on intracellular second messengers and genomic mechanisms which are crucially involved in the regulation of excitotoxic and apoptotic cascades. It is still an open question whether in the foreseeable future the presented direction of research will allow us to regulate endogenous anticonvulsant and neuroprotective mechanisms in a subtle way in order to substitute for or support other forms of treatment.
Related Concept Videos
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
Antiepileptic Drugs: GABAergic Pathway Potentiators
The key GABA pathway potentiators used in epilepsy management are as follows.
Benzodiazepines are a well-known class of drugs used for their...
Antiepileptic Drugs: Glutamate Antagonists
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...
Antiepileptic Drugs: Calcium Channel Blockers
Calcium channel blockers exert their antiepileptic effects by targeting T-type calcium channels, which are integral to transmitting nerve signals in the central nervous system. These channels allow the passage of calcium ions, which are vital for neuronal communication. By inhibiting T-type calcium channels, calcium channel blockers effectively reduce the release of neurotransmitters and...
Antiepileptic Drugs: Sodium Channel Blockers
Sodium channel blockers modulate ion channels, particularly voltage-gated sodium channels. They block only sodium ion movement.
Among the most commonly prescribed antiepileptic drugs are...
