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		<title>Toxins: Marine Biotoxins: Novel Issues about Old Compounds</title>
		<link>http://www.mdpi.com/journal/toxins/special_issues/marine-biotoxins/</link>
		<description>Dear Colleagues, 

Human poisonings due to exposures to marine biotoxins have occurred in  the past and represent naturally occurring events, that have been  attracting an increasing interest from the scientific community. 

The last ten years, in particular, have witnessed a growing body of  knowledge on the chemistry, mechanisms of action, toxicity, ecology and  distribution, as well as the health impact of marine biotoxins. Research  efforts have led to a deeper understanding of many aspects of marine  biotoxins and their impact on living organisms, while novel issues have  been recognized. For instance, “new” toxin producers have been  identified, and “old” ones are being characterized using molecular  probes. The number of toxins isolated, chemically characterized and/or  synthesized has increased, and new groups of biotoxins have been  discovered. Likewise, the methodology for toxin detection has been  continuously developed, providing both instrumental and bio-molecular  options. Biochemical tools have been increasingly used to clarify the  mechanisms of action of toxins, and the “omic” approaches have entered  the biotoxin field. The toxicology of biotoxins has been advancing,  taking into consideration the real conditions of human and animal  exposure to these compounds. 

It’s time to gather the information available on novel issues in marine  biotoxins, to critically evaluate what we know and pinpoint the many  unknowns, thereby providing a broad perspective to support the  scientific community in its next efforts to understand and exploit the  complexity of the chemistry and biology of marine biotoxins. 

Prof. Dr. Gian Paolo Rossini 
Guest Editor 
Related Special Issues in other Journals
Marine Biotoxins: Novel Issues about Old Compounds in Marine Drugs
Submission 

All papers should be submitted to toxins@mdpi.com with copy to the guest editor. To be published continuously until the deadline and papers will be listed together at the special websites.
Submitted papers should not have been previously published nor be currently under consideration for publication elsewhere. All papers are refereed through a peer review process. A guide for authors, sample copies and other relevant information for submitting papers are available on the Instructions for Authors page. Toxins is an international peer-reviewed monthly journal published by MDPI.

Article Processing Charges (APC) for publication in this  open access journal are waived for well-prepared manuscripts submitted by 30 June 2010. English correction or formatting fees of 250 CHF (Swiss Francs) will be charged in certain cases for those paper accepted for publication, that require extensive additional formatting and/or English corrections.</description>
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	<title>Toxins, Vol. 2, Pages 1646-1675: Neurological Disease Rises from Ocean to Bring Model for Human Epilepsy to Life</title>
	<link>http://www.mdpi.com/2072-6651/2/7/1646/</link>
	<description>Domoic acid of macroalgal origin was used for traditional and medicinal purposes in Japan and largely forgotten until its rediscovery in diatoms that poisoned 107 people after consumption of contaminated mussels. The more severely poisoned victims had seizures and/or amnesia and four died; however, one survivor unexpectedly developed temporal lobe epilepsy (TLE) a year after the event. Nearly a decade later, several thousand sea lions have stranded on California beaches with neurological symptoms. Analysis of the animals stranded over an eight year period indicated five clusters of acute neurological poisoning; however, nearly a quarter have stranded individually outside these events with clinical signs of a chronic neurological syndrome similar to TLE. These poisonings are not limited to sea lions, which serve as readily observed sentinels for other marine animals that strand during domoic acid poisoning events, including several species of dolphin and whales. Acute domoic acid poisoning is five-times more prominent in adult female sea lions as a result of the proximity of their year-round breeding grounds to major domoic acid bloom events. The chronic neurological syndrome, on the other hand, is more prevalent in young animals, with many potentially poisoned in utero. The sea lion rookeries of the Channel Islands are at the crossroads of domoic acid producing harmful algal blooms and a huge industrial discharge site for dichlorodiphenyltrichloroethane (DDTs). Studies in experimental animals suggest that chronic poisoning observed in immature sea lions may result from a spatial and temporal coincidence of DDTs and domoic acid during early life stages. Emergence of an epilepsy syndrome from the ocean brings a human epilepsy model to life and provides unexpected insights into interaction with legacy contaminants and expression of disease at different life stages.</description>
	
	<guid>http://www.mdpi.com/2072-6651/2/7/1646/</guid>
	<pubDate>Mon, 28 Jun 2010 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Toxins</prism:publicationName>
	<prism:publicationDate>2010-06-28</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>1646</prism:startingPage>
		<prism:endingPage>1675</prism:endingPage>
		<prism:issn>2072-6651</prism:issn>
	
	<dc:title>Neurological Disease Rises from Ocean to Bring Model for Human Epilepsy to Life</dc:title>
	<dc:date>2010-06-28</dc:date>
	<dc:identifier>doi: 10.3390/toxins2071646</dc:identifier>
		<dc:creator> Ramsdell</dc:creator>
	
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	<title>Toxins, Vol. 2, Pages 195-204: PP2A Inhibition Assay Using Recombinant Enzyme for Rapid Detection of Okadaic Acid and Its Analogs in Shellfish</title>
	<link>http://www.mdpi.com/2072-6651/2/1/195/</link>
	<description>Okadaic acid and its analogs (OAs) responsible for diarrhetic shellfish poisoning (DSP) strongly inhibit protein phosphatase 2A (PP2A) and thus are quantifiable by measuring the extent of the enzyme inhibition. In this study, we evaluated the suitability of the catalytic subunit of recombinant human PP2A (rhPP2Ac) for use in a microplate OA assay. OA, dinophysistoxin-1(DTX1), and hydrolyzate of 7-O-palmitoyl-OA strongly inhibited rhPP2Ac activity with IC50 values of 0.095, 0.104, and 0.135 nM, respectively. The limits of detection and quantitation for OA in the digestive gland of scallops and mussels were 0.0348 μg/g and 0.0611 μg/g respectively, and, when converted to the whole meat basis, are well below the regulation level proposed by EU (0.16 μg/g whole meat). A good correlation with LC-MS data was demonstrated, the correlation coefficient being 0.996 with the regression slope of 1.097.</description>
	
	<guid>http://www.mdpi.com/2072-6651/2/1/195/</guid>
	<pubDate>Mon, 25 Jan 2010 00:00:00 CET</pubDate>
	
	<prism:publicationName>Toxins</prism:publicationName>
	<prism:publicationDate>2010-01-25</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>195</prism:startingPage>
		<prism:endingPage>204</prism:endingPage>
		<prism:issn>2072-6651</prism:issn>
	
	<dc:title>PP2A Inhibition Assay Using Recombinant Enzyme for Rapid Detection of Okadaic Acid and Its Analogs in Shellfish</dc:title>
	<dc:date>2010-01-25</dc:date>
	<dc:identifier>doi: 10.3390/toxins2010195</dc:identifier>
		<dc:creator>Tsuyoshi Ikehara</dc:creator>
		<dc:creator>Shihoko Imamura</dc:creator>
		<dc:creator>Atsushi Yoshino</dc:creator>
		<dc:creator>Takeshi Yasumoto</dc:creator>
	
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