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Centipedes subdue giant prey by blocking KCNQ channels.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2018 Feb 13; Vol. 115 (7), pp. 1646-1651. Date of Electronic Publication: 2018 Jan 22. - Publication Year :
- 2018
-
Abstract
- Centipedes can subdue giant prey by using venom, which is metabolically expensive to synthesize and thus used frugally through efficiently disrupting essential physiological systems. Here, we show that a centipede ( Scolopendra subspinipes mutilans , ∼3 g) can subdue a mouse (∼45 g) within 30 seconds. We found that this observation is largely due to a peptide toxin in the venom, SsTx, and further established that SsTx blocks KCNQ potassium channels to exert the lethal toxicity. We also demonstrated that a KCNQ opener, retigabine, neutralizes the toxicity of a centipede's venom. The study indicates that centipedes' venom has evolved to simultaneously disrupt cardiovascular, respiratory, muscular, and nervous systems by targeting the broadly distributed KCNQ channels, thus providing a therapeutic strategy for centipede envenomation.<br />Competing Interests: The authors declare no conflict of interest.<br /> (Copyright © 2018 the Author(s). Published by PNAS.)
- Subjects :
- Animals
Anticonvulsants pharmacology
Carbamates pharmacology
Mice
Nervous System Diseases drug therapy
Nervous System Diseases metabolism
Phenylenediamines pharmacology
Respiratory System Abnormalities drug therapy
Respiratory System Abnormalities metabolism
Arthropod Venoms toxicity
Arthropods physiology
KCNQ Potassium Channels antagonists & inhibitors
Nervous System Diseases chemically induced
Predatory Behavior drug effects
Respiratory System Abnormalities chemically induced
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 115
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 29358396
- Full Text :
- https://doi.org/10.1073/pnas.1714760115