Pyrethroids
are one of the most commonly used classes of insecticides,
and their acid and alcohol components are esterase degradation products,
usually considered to be biologically inactive. In this study, it
was found that several pyrethroid acids had a spatial repellent activity
that was greater than DEET, often more active than the parent pyrethroids,
and showed little cross resistance in a pyrethroid-resistant Puerto
Rico strain of Aedes aegypti mosquitoes. Further
investigation revealed that the acids can synergize not only contact
repellent standards but also other pyrethroid components as well as
the parent pyrethroids themselves. Synergism by the pyrethroid acids
is expressed as both increased spatial repellency and vapor toxicity
as well as human bite protection. Electrophysiological studies confirmed
that pyrethroid acids (100 μM) had no effect on neuronal discharge
in larval Drosophila melanogaster CNS and were detected
by electroantennography, and there was little resistance to olfactory
sensing of these acids in antennae from Puerto Rico strain mosquitoes
carrying kdr mutations. Thus, the data suggest that the pyrethroid
acids have a different mode of action than the parent pyrethroids,
unrelated to the voltage-sensitive sodium channel. The results highlight
the potential of pyrethroid acids to be useful in future repellent
formulations.
BackgroundHypocretin peptides participate in the regulation of sleep-wake cycle while deficiency in hypocretin signaling and loss of hypocretin neurons are causative for narcolepsy-cataplexy. However, the mechanism responsible for alteration of the hypocretin system in narcolepsy-cataplexy and its relevance to other central hypersomnias remain unknown. Here we studied whether central hypersomnias can be associated with autoantibodies reacting with hypocretin-1 peptide present as immune complexes.MethodologySerum levels of free and dissociated (total) autoantibodies reacting with hypocretin-1 peptide were measured by enzyme-linked immunosorbent assay and analyzed with regard to clinical parameters in 82 subjects with narcolepsy-cataplexy, narcolepsy without cataplexy or idiopathic hypersomnia and were compared to 25 healthy controls.Principal FindingsSerum levels of total but not free IgG autoantibodies against hypocretin-1 were increased in narcolepsy-cataplexy. Increased levels of complexed IgG autoantibodies against hypocretin-1 were found in all patients groups with a further increase in narcolepsy-cataplexy. Levels of total IgM hypocretin-1 autoantibodies were also elevated in all groups of patients. Increased levels of anti-idiotypic IgM autoantibodies reacting with hypocretin-1 IgG autoantibodies affinity purified from sera of subjects with narcolepsy-cataplexy were found in all three groups of patients. Disease duration correlated negatively with serum levels of hypocretin-1 IgG and IgM autoantibodies and with anti-idiotypic IgM autoantibodies.ConclusionCentral hypersomnias and particularly narcolepsy-cataplexy are characterized by higher serum levels of autoantibodies directed against hypocretin-1 which are present as immune complexes most likely with anti-idiotypic autoantibodies suggesting their relevance to the mechanism of sleep-wake cycle regulation.
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