Abstract
Neurocysticercosis (NCC), a helminth infection of the brain, is a major cause of seizures. The mediators responsible for seizures in NCC are unknown, and their management remains controversial. Substance P (SP) is a neuropeptide produced by neurons, endothelial cells and immunocytes. The current studies examined the hypothesis that SP mediates seizures in NCC. We demonstrated by immunostaining that 5 of 5 brain biopsies from NCC patients contained substance P (SP)-positive (+) cells adjacent to but not distant from degenerating worms; no SP+ cells were detected in uninfected brains. In a rodent model of NCC, seizures were induced after intrahippocampal injection of SP alone or after injection of extracts of cysticercosis granuloma obtained from infected wild type (WT), but not from infected SP precursor-deficient mice. Seizure activity correlated with SP levels within WT granuloma extracts and was prevented by intrahippocampal pre-injection of SP receptor antagonist. Furthermore, extracts of granulomas from WT mice caused seizures when injected into the hippocampus of WT mice, but not when injected into SP receptor (NK1R) deficient mice. These findings indicate that SP causes seizures in NCC, and, suggests that seizures in NCC in humans may be prevented and/or treated with SP-receptor antagonists.
Highlights
Neurocysticercosis (NCC) is a parasitic infection of the human central nervous system that is caused by the pig tapeworm Taenia solium
Neurocysticercosis (NCC), is a helminth infection of the brain that is caused by Taenia solium
Seizures are thought to result not from parasitic infection per se, but from the chronic granulomatous host response initiated by dying cysts
Summary
Neurocysticercosis (NCC) is a parasitic infection of the human central nervous system that is caused by the pig tapeworm Taenia solium. Live T. solium cysts in the brain of NCC patients are surrounded by little or no inflammation. Seizures are thought to result from the granulomatous host response initiated by dead or dying cysts rather than mediators produced by the parasite itself [5,8,9,10,11]. The mediators responsible for inducing seizures in NCC are not known; their identification may lead to more effective strategies for prevention and/or treatment of seizures in this disease. Receptors for SP (NK1R) are expressed by cells within and outside the central nervous system including neurons, endothelial cells and immunocytes [12,13,14,15,16]. A few reports implicate SP in the pathogenesis of seizures including one in which SP amplified seizure responses in rats [18,19]
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