Toxicity and possible mechanisms of action of honokiol from Magnolia denudata seeds against four mosquito species View Full Text


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Article Info

DATE

2019-12

AUTHORS

Zhangqian Wang, Haribalan Perumalsamy, Xue Wang, Young-Joon Ahn

ABSTRACT

This study was performed to determine the toxicity and possible mechanism of the larvicidal action of honokiol, extracted from Magnolia denudata seeds, and its 10 related compounds against third-instar larvae of insecticide-susceptible Culex pipiens pallens, Aedes aegypti, and Aedes albopictus and Anopheles sinensis resistant to deltamethrin and temephos. Honokiol (LC50, 6.13-7.37 mg/L) was highly effective against larvae of all of the four mosquito species, although the toxicity of the compound was lower than that of the synthetic larvicide temephos. Structure-activity relationship analyses indicated that electron donor and/or bulky groups at the ortho or para positions of the phenol were required for toxicity. Honokiol moderately inhibited acetylcholinesterase and caused a considerable increase in cyclic AMP levels, indicating that it might act on both acetylcholinesterase and octopaminergic receptors. Microscopy analysis clearly indicated that honokiol was mainly targeted to the midgut epithelium and anal gills, resulting in variably dramatic degenerative responses of the midgut through sequential epithelial disorganization. Honokiol did not affect the AeCS1 mRNA expression level in Ae. aegypti larvae, but did enhance expression of the genes encoding vacuolar-type H+-ATPase and aquaporin 4, indicating that it may disturb the Na+, Cl- and K+ co-transport systems. These results demonstrate that honokiol merits further study as a potential larvicide, with a specific target site, and as a lead molecule for the control of mosquito populations. More... »

PAGES

411

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/s41598-018-36558-y

    DOI

    http://dx.doi.org/10.1038/s41598-018-36558-y

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1111612944

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/30674912


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