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Chloride channels in parasites, particularly those that are parasite-specific, represent a diverse group of ion channels critical for parasite physiology and survival. These channels are often distinct from their mammalian counterparts, making them attractive targets for selective antiparasitic drug development. Examples include glutamate-gated chloride channels (GluCl) in nematodes, acetylcholine-gated chloride channels, and the plasmodial surface anion channel (PSAC) in malaria parasites. These channels are essential for neuromuscular function, osmoregulation, nutrient uptake, and the survival and infectivity of parasitic stages. Many successful anthelmintics act on these channels due to their absence or significant divergence from host homologs, allowing high selectivity with reduced host toxicity.
Ligand binding opens Cl⁻ permeable pore; causes hyperpolarization/paralysis
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