Toxicity and possible mechanisms of action of honokiol from Magnolia denudata seeds against four mosquito species
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...
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Published in | Scientific reports Vol. 9; no. 1; p. 411 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
23.01.2019
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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 (LC
50
, 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. |
---|---|
AbstractList | 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 (LC
50
, 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. 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. 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 (LC , 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. |
ArticleNumber | 411 |
Author | Wang, Xue Wang, Zhangqian Perumalsamy, Haribalan Ahn, Young-Joon |
Author_xml | – sequence: 1 givenname: Zhangqian surname: Wang fullname: Wang, Zhangqian organization: Department of Agricultural Biotechnology, Seoul National University, Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University), Ministry of Education, and Wuhan University School of Pharmaceutical Sciences – sequence: 2 givenname: Haribalan surname: Perumalsamy fullname: Perumalsamy, Haribalan organization: Research Institute of Agriculture and Life Sciences, Seoul National University – sequence: 3 givenname: Xue surname: Wang fullname: Wang, Xue organization: School of Pharmaceutical Science, Wenzhou Medical University – sequence: 4 givenname: Young-Joon surname: Ahn fullname: Ahn, Young-Joon email: yjahn@snu.ac.kr organization: Department of Agricultural Biotechnology, Seoul National University, Research Institute of Agriculture and Life Sciences, Seoul National University |
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Snippet | This study was performed to determine the toxicity and possible mechanism of the larvicidal action of honokiol, extracted from
Magnolia denudata
seeds, and its... This study was performed to determine the toxicity and possible mechanism of the larvicidal action of honokiol, extracted from Magnolia denudata seeds, and its... |
SourceID | pubmedcentral proquest crossref pubmed springer |
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Title | Toxicity and possible mechanisms of action of honokiol from Magnolia denudata seeds against four mosquito species |
URI | https://link.springer.com/article/10.1038/s41598-018-36558-y https://www.ncbi.nlm.nih.gov/pubmed/30674912 https://www.proquest.com/docview/2170389966 https://pubmed.ncbi.nlm.nih.gov/PMC6344527 |
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