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Gymnodimine A and 13-desMethyl Spirolide C Alter Intracellular Calcium Levels via Acetylcholine Receptors
by
Nieva, Joyce A.
, Tillmann, Urban
, Tebben, Jan
, Zurhelle, Christian
, Bickmeyer, Ulf
, Krock, Bernd
in
Alexandrium ostenfeldii
/ calcium signaling
/ cyclic imine
/ nicotinic, muscarinic, and acetylcholine receptors
2020
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Gymnodimine A and 13-desMethyl Spirolide C Alter Intracellular Calcium Levels via Acetylcholine Receptors
by
Nieva, Joyce A.
, Tillmann, Urban
, Tebben, Jan
, Zurhelle, Christian
, Bickmeyer, Ulf
, Krock, Bernd
in
Alexandrium ostenfeldii
/ calcium signaling
/ cyclic imine
/ nicotinic, muscarinic, and acetylcholine receptors
2020
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Do you wish to request the book?
Gymnodimine A and 13-desMethyl Spirolide C Alter Intracellular Calcium Levels via Acetylcholine Receptors
by
Nieva, Joyce A.
, Tillmann, Urban
, Tebben, Jan
, Zurhelle, Christian
, Bickmeyer, Ulf
, Krock, Bernd
in
Alexandrium ostenfeldii
/ calcium signaling
/ cyclic imine
/ nicotinic, muscarinic, and acetylcholine receptors
2020
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Gymnodimine A and 13-desMethyl Spirolide C Alter Intracellular Calcium Levels via Acetylcholine Receptors
Journal Article
Gymnodimine A and 13-desMethyl Spirolide C Alter Intracellular Calcium Levels via Acetylcholine Receptors
2020
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Overview
Gymnodimines and spirolides are cyclic imine phycotoxins and known antagonists of nicotinic acetylcholine receptors (nAChRs). We investigated the effect of gymnodimine A (GYM A) and 13-desmethyl spirolide C (SPX 1) from Alexandrium ostenfeldii on rat pheochromocytoma (PC12) cells by monitoring intracellular calcium levels ([Ca]i). Using whole cells, the presence of 0.5 µM of GYM A or SPX 1 induced an increase in [Ca]i mediated by acetylcholine receptors (AChRs) and inhibited further activation of AChRs by acetylcholine (ACh). To differentiate the effects of GYM A or SPX 1, the toxins were applied to cells with pharmacologically isolated nAChRs and muscarinic AChRs (mAChRs) as mediated by the addition of atropine and tubocurarine, respectively. GYM A and SPX 1 activated nAChRs and inhibited the further activation of nAChRs by ACh, indicating that both toxins mimicked the activity of ACh. Regarding mAChRs, a differential response was observed between the two toxins. Only GYM A activated mAChRs, resulting in elevated [Ca]i, but both toxins prevented a subsequent activation by ACh. The absence of the triketal ring system in GYM A may provide the basis for a selective activation of mAChRs. GYM A and SPX 1 induced no changes in [Ca]i when nAChRs and mAChRs were inhibited simultaneously, indicating that both toxins target AChRs.
Publisher
MDPI,MDPI AG
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