Emodepside
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| ECHA InfoCard | 100.123.218 |
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| Formula | C60H90N6O14 |
| Molar mass | 1119.408 g·mol−1 |
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Emodepside is an anthelmintic drug that is effective against a number of gastrointestinal nematodes, is licensed for use in cats[1] and belongs to the class of drugs known as the octadepsipeptides,[2] a relatively new class of anthelmintic (research into these compounds began in the early 1990s),[3] which are suspected to achieve their anti-parasitic effect by a novel mechanism of action due to their ability to kill nematodes resistant to other anthelmintics.[4]
Synthesis
[edit]
Emodepside is synthesised by attaching a morpholine ring “at the paraposition of each of the two D-phenyllactic acids” to PF1022A, a metabolite of Mycelia sterile, a fungus that inhabits the leaves of Camellia japonica[3] – a flowering shrub.
Anthelmintic effects
[edit]When applied to nematodes, emodepside has been shown to have a range of effects, inhibiting muscle in the parasitic nematode Ascaris sum,[5] and inhibiting locomotive and pharyngeal movement in Caenorhabditis elegans in addition to having effects in other tissues such as the inhibition of egg laying.[6]
Mechanism of action
[edit]One of the ways in which this drug achieves its effects has been shown to be through binding to a group of G-protein coupled receptors called latrophilins,[6] first identified as being target proteins for α-latrotoxin (the other target protein of α-LTX being neurexin,[7] a membrane receptor with laminin-like extracellular domains[8]), a component of black widow spider venom that can cause paralysis and subsequent death in nematodes and humans alike. LAT-1 (1014 amino acids, 113 KDa coded by the B0457.1 gene) and LAT-2 (1338 amino acids, 147 KDa coded by the B0286.2 gene)[9] are located presynaptically at the neuromuscular junction in Caenorhabditis elegans[2] and share 21% amino acid identity with each other[6] (the amino acid sequence homology LAT-1 shares with rat, bovine and human latrophilins has been shown to be 22, 23 and 21% respectively[6]).
Following receptor-ligand binding, a conformational change induced in the receptor activates the Gq protein, freeing the Gqα subunit from the βγ complex. The Gqα protein then goes on to couple-to and activate the signaling molecule phospholipase-C-β, a protein that has been identified as being key to the modulation of regulatory pathways of vesicle release in C.elegans.[6]
In its signaling cascade, PLC-β (like other phospholipases) hydrolyses phosphatidylinositolbisphosphate to yield inositol trisphosphate (IP3) and diacylglycerol (DAG).[10] As IP3 receptors have sparse or little distribution throughout the pharyngeal nervous system of C.elegans[11] (one of the tissues where LAT-1 agonists such as α-LTX and emodepside have their most predominant effects)[6] and β-phorbel esters (which mimic the effects of DAG) have been shown to have a stimulatory action on synaptic transmission,[12] it has been concluded that it is the DAG component of the cascade that regulates neurotransmitter release.[6]
Indeed, in C.elegans DAG regulates UNC-13, a plasma-membrane associated protein critical for vesicle-mediated neurotransmitter release[13] and mutational studies have shown that two UNC-13 reduction of function mutants show resistance to emodepside, observations supporting this hypothesized mechanism of action. The mechanism by which activation of UNC-13 results in neurotransmitter release (the ultimate result of latrophilin activation) is through interaction with the synaptosomal membrane protein syntaxin,[6][14] with UNC-13 binding to the N-terminus of syntaxin and promoting the switch from the closed form of syntaxin (which is incompatible with SNARE complex synaptobrevin, SNAP-25 and syntaxin formation) to its open formation so that SNARE complex formation can be achieved, thereby allowing vesicle fusion and release to take place.[14]
At a molecular level, the net result of the activation of this pathway, is the spontaneous stimulation of inhibitory PF1-like neuropeptide release (this is suspected due to Emodepside's inhibition of acetylcholine-elicited muscle contraction requiring both calcium ions and extracellular potassium ions, similar to the action of PF1/PF2). Although in experiments on synaptosomes, α-LTX triggered non-calcium dependent exocytosis of vesicles containing acetylcholine, glutamate and GABA,[15] both glutamate[6] and GABA[15] have been ruled out as the sole neurotransmitters responsible for emodepside's action) which then acts on the post-synaptic membrane (i.e. the pharyngeal/muscle membrane) of the nematode, having an inhibitory effect thereby either inducing paralysis or inhibiting pharyngeal pumping, both of which ultimately result in the death of the organism.[citation needed]
Mutational studies involving LAT-1 knockout and LAT-2 gene deletion mutants have revealed that the role of latrophilin receptors in the different tissues that they are expressed differs between subtypes, with LAT-1 being expressed in the pharynx of C.elegans (thereby modulating pharyngeal pumping) and LAT-2 having a role in locomotion.[6]
In addition to exerting an effect on the nematode via binding to Latrophilin receptors, there is also recent evidence that indicates that emodepside also interacts with the BK potassium channel coded by the gene Slo-1.[16] This protein (see figure for structure) is a member of the 6 transmembrane helix structural class of potassium ion channels with each subunit consisting of 6 transmembrane helices and 1 P domain (this P domain is conserved in all potassium ion channels and forms the selectivity filter that enables the channel to transport potassium ions across the membrane in great preference to other ions).[17] These subunits group together to form high conductance BK-type channels that are gated by both membrane potential and intracellular calcium levels[17] (this calcium ion sensing ability is accommodated by an intracellular tail region on Slo-like subunits that form a calcium ion binding motif consisting of a run of conserved aspartate residues, termed a “calcium bowl”),[18] with their physiological role being to regulate the excitability of neurons and muscle fibres, through the way in which they participate in action potential repolariziation (with potassium ion efflux being used to repolarize the cell following depolarization).[19]
The presumable effect that emodepside interaction with these channels would exert on the neuron would be to activate the channel causing potassium ion efflux, hyper-polarization and subsequent inhibition of excitatory neurotransmitter effect (acetylcholine if acting at the neuromuscular junction), having an inhibitory effect on synaptic transmission, the production of postsynaptic action potentials and ultimately muscle contraction (manifesting itself as paralysis or reduced pharyngeal pumping).[citation needed]
Which out of Latrophilin receptors and BK-potassium channels is emodepside's primary site of action remains to be completely deduced. Both LAT-1/LAT-2 and slo-1 mutants (reduction/loss of function) show significant resistance to emodepside with it being conceivable that the presence of both is required for emodepside to induce its full effect.[citation needed]
Therapeutic use
[edit]The patent for emodepside is owned by the Bayer Health Care group and is sold in combination with another anthelmintic (praziquantel) for topical application under the tradename Profender.[20][21][22]
References
[edit]- ^ "Profender? Spot-on at a glance". Archived from the original on 2007-01-11. Retrieved 2007-01-10.
- ^ a b Willson J, Amliwala K, Harder A, Holden-Dye L, Walker RJ (January 2003). "The effect of the anthelmintic emodepside at the neuromuscular junction of the parasitic nematode Ascaris suum". Parasitology. 126 (Pt 1): 79–86. doi:10.1017/S0031182002002639. PMID 12613766. S2CID 21831523.
- ^ a b Harder A, Holden-Dye L, Walker R, Wunderlich F (October 2005). "Mechanisms of action of emodepside". Parasitology Research. 97 (Suppl 1): S1–S10. doi:10.1007/s00436-005-1438-z. PMID 16228263. S2CID 86636553.
- ^ Harder A, Schmitt-Wrede HP, Krücken J, Marinovski P, Wunderlich F, Willson J, et al. (September 2003). "Cyclooctadepsipeptides--an anthelmintically active class of compounds exhibiting a novel mode of action". International Journal of Antimicrobial Agents. 22 (3): 318–331. doi:10.1016/S0924-8579(03)00219-X. PMID 13678839.
- ^ Geßner G, Meder S, Rink T, Boheim G, Harder A, Jeschke P, Scherkenbeck J, Londershausen M (December 1996). "Ionophore and anthelmintic activity of PF 1022A, a cyclooctadepsipeptide, are not related". Pesticide Science. 48 (4): 399–407. doi:10.1002/(SICI)1096-9063(199612)48:4<399::AID-PS503>3.0.CO;2-K.
- ^ a b c d e f g h i j Willson J, Amliwala K, Davis A, Cook A, Cuttle MF, Kriek N, et al. (August 2004). "Latrotoxin receptor signaling engages the UNC-13-dependent vesicle-priming pathway in C. elegans". Current Biology. 14 (15): 1374–1379. Bibcode:2004CBio...14.1374W. doi:10.1016/j.cub.2004.07.056. PMID 15296755.
- ^ Davletov BA, Meunier FA, Ashton AC, Matsushita H, Hirst WD, Lelianova VG, et al. (July 1998). "Vesicle exocytosis stimulated by alpha-latrotoxin is mediated by latrophilin and requires both external and stored Ca2+". The EMBO Journal. 17 (14): 3909–3920. doi:10.1093/emboj/17.14.3909. PMC 1170726. PMID 9670008.
- ^ Saibil HR (January 2000). "The black widow's versatile venom". Nature Structural Biology. 7 (1): 3–4. doi:10.1038/71190. PMID 10625413. S2CID 28185969.
- ^ a b "Wormbase". Archived from the original on 2017-04-20. Retrieved 2022-01-15.
- ^ The molecular biology of the cell - Alberts et al.
- ^ Baylis HA, Furuichi T, Yoshikawa F, Mikoshiba K, Sattelle DB (November 1999). "Inositol 1,4,5-trisphosphate receptors are strongly expressed in the nervous system, pharynx, intestine, gonad and excretory cell of Caenorhabditis elegans and are encoded by a single gene (itr-1)". Journal of Molecular Biology. 294 (2): 467–476. doi:10.1006/jmbi.1999.3229. PMID 10610772.
- ^ Majewski H, Iannazzo L (August 1998). "Protein kinase C: a physiological mediator of enhanced transmitter output". Progress in Neurobiology. 55 (5): 463–475. doi:10.1016/S0301-0082(98)00017-3. PMID 9670214. S2CID 9063590.
- ^ Aravamudan B, Fergestad T, Davis WS, Rodesch CK, Broadie K (November 1999). "Drosophila UNC-13 is essential for synaptic transmission". Nature Neuroscience. 2 (11): 965–971. doi:10.1038/14764. PMID 10526334. S2CID 24641836.
- ^ a b Söllner T, Bennett MK, Whiteheart SW, Scheller RH, Rothman JE (November 1993). "A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion". Cell. 75 (3): 409–418. doi:10.1016/0092-8674(93)90376-2. PMID 8221884. S2CID 26906457.
- ^ a b Khvotchev M, Lonart G, Südhof TC (2000). "Role of calcium in neurotransmitter release evoked by alpha-latrotoxin or hypertonic sucrose". Neuroscience. 101 (3): 793–802. doi:10.1016/s0306-4522(00)00378-x. PMID 11113328. S2CID 54256700.
- ^ Willson J, Holden-Dye L, Harder A, Walker RJ (November 2001). "A possible mechanism for the action of the novel anthelmintic emodepside, using Ascaris suum body wall muscle preparations". Journal of Physiology. 536 (S103): 132P–133P.
- ^ a b Salkoff L, Wei AD, Baban B, Butler A, Fawcett G, Ferreira G, Santi CM (December 2005). "Potassium channels in C. elegans". WormBook: The Online Review of C. Elegans Biology: 1–15. doi:10.1895/wormbook.1.42.1. PMC 4781360. PMID 18050399.
- ^ Schreiber M, Salkoff L (September 1997). "A novel calcium-sensing domain in the BK channel". Biophysical Journal. 73 (3): 1355–1363. Bibcode:1997BpJ....73.1355S. doi:10.1016/S0006-3495(97)78168-2. PMC 1181035. PMID 9284303.
- ^ Araque A, Buño W (October 1999). "Fast BK-type channel mediates the Ca(2+)-activated K(+) current in crayfish muscle". Journal of Neurophysiology. 82 (4): 1655–1661. doi:10.1152/jn.1999.82.4.1655. PMID 10515956.
- ^ Altreuther G, Buch J, Charles SD, Davis WL, Krieger KJ, Radeloff I (October 2005). "Field evaluation of the efficacy and safety of emodepside/praziquantel spot-on solution against naturally acquired nematode and cestode infections in domestic cats". Parasitology Research. 97 (Suppl 1): S58–S64. doi:10.1007/s00436-005-1445-0. PMID 16228276. S2CID 3324872.
- ^ "Profender EPAR". European Medicines Agency (EMA). 27 July 2005. Retrieved 26 December 2024.
- ^ "Profender PI". Union Register of medicinal products. 29 July 2005. Retrieved 26 December 2024.