<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns="http://purl.org/rss/1.0/"
    xmlns:cc="http://web.resource.org/cc/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
	<channel rdf:about="http://www.mdpi.com/rss/special_issue/mar-comp-act-reprod">
		<title>Marine Drugs: Marine Bioactive Compounds Acting on Animal Reproduction</title>
		<link>http://www.mdpi.com/journal/marinedrugs/special_issues/mar-comp-act-reprod/</link>
		<description>Dear Colleagues, 

Reproduction is a step by step process that starts at the production of  gametes (gametogenesis), proceeds with their activation and interaction  (fertilization) and virtually ends when full embryo development leads to  the formation of a new adult individual. Electrical, morphological and  biochemical modifications occurring through all the steps of the  reproductive process  involve ion channels activity, calcium release and  oscillations, molecules, metabolites and messengers of different  natures. Although it is known  that  marine-derived bioactive substances  act on a series of biological processes, little is known on  marine  drugs affecting  specific reproductive molecular dynamics. On the  contrary, many information are available on marine natural products  whose target molecules play a key role in the main steps of  gametogenesis, fertilization and embryo development. The aim of this  special issue is to report respectively i) the recognized impact of  marine drugs of different origin on the reproductive process in animals;  ii) their potential but unexplored role on the  molecular mechanisms  involved in the animal reproduction. 

Elisabetta Tosti, Ph. D. 
Guest Editor
Submission Information

All papers should be submitted to marinedrugs@mdpi.com with copy to the Editors. To be published continuously until the deadline and papers will be listed together at the special websites. Both, research articles and review articles are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editors for announcment on this website.

Submitted papers should not have been published previously, nor be 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. Marine Drugs is an international peer-reviewed quarterly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a paper Open Access publication fees are 1000 CHF per paper. English correction fees (250 CHF) will be added in certain cases (1250 CHF per paper for those papers that require extensive additional formatting and/or English corrections.).</description>
								<items>
			<rdf:Seq>
							<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/9/8/1359/" />
            				<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/8/4/950/" />
            				<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/8/4/881/" />
            				<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/8/3/471/" />
            				<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/8/1/59/" />
            				<rdf:li rdf:resource="http://www.mdpi.com/1660-3397/7/3/367/" />
                    	</rdf:Seq>
		</items>
				<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
	</channel>
	<item rdf:about="http://www.mdpi.com/1660-3397/9/8/1359/">
	<title>Marine Drugs, Vol. 9, Pages 1359-1367: Fucoidan from Marine Brown Algae Inhibits Lipid Accumulation</title>
	<link>http://www.mdpi.com/1660-3397/9/8/1359/</link>
	<description>In this study, we elucidated the inhibitory effect of fucoidan from marine brown algae on the lipid accumulation in differentiated 3T3-L1 adipocytes and its mechanism. The treatment of fucoidan in a dose-dependent manner was examined on lipid inhibition in 3T3-L1 cells by using Oil Red O staining. Fucoidan showed high lipid inhibition activity at 200 µg/mL concentration (P &lt; 0.001). Lipolytic activity in adipocytes is highly dependent on hormone sensitive lipase (HSL), which is one of the most important targets of lipolytic regulation. Here, we examined the biological response of fucoidan on the protein level of lipolysis pathway. The expressed protein levels of total hormone sensitive lipase (HSL) and its activated form, phosphorylated-HSL were significantly increased at concentration of 200 µg/mL fucoidan. Furthermore, insulin-induced 2-deoxy-D-[3H] glucose uptake was decreased up to 51% in fucoidan-treated cells as compared to control. Since increase of HSL and p-HSL expression and decrease of glucose uptake into adipocytes are known to lead to stimulation of lipolysis, our results suggest that fucoidan reduces lipid accumulation by stimulating lipolysis. Therefore, these results suggest that fucoidan can be useful for the prevention or treatment of obesity due to its stimulatory lipolysis.</description>
	
	<guid>http://www.mdpi.com/1660-3397/9/8/1359/</guid>
	<pubDate>Wed, 10 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2011-08-10</prism:publicationDate>
	<prism:volume>9</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1359</prism:startingPage>
		<prism:endingPage>1367</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>Fucoidan from Marine Brown Algae Inhibits Lipid Accumulation</dc:title>
	<dc:date>2011-08-10</dc:date>
	<dc:identifier>doi: 10.3390/md9081359</dc:identifier>
		<dc:creator>Min-Kyoung Park</dc:creator>
		<dc:creator>Uhee Jung</dc:creator>
		<dc:creator>Changhyun Roh</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1660-3397/8/4/950/">
	<title>Marine Drugs, Vol. 8, Pages 950-967: Teratogenic Effects of Diatom Metabolites on Sea Urchin Paracentrotus lividus Embryos</title>
	<link>http://www.mdpi.com/1660-3397/8/4/950/</link>
	<description>The diatom-derived polyunsaturated aldehydes (PUAs), 2-trans,4-trans-decadienal, 2-trans,4-trans-octadienal, 2-trans,4-trans,7-octatrienal, 2-trans,4-trans-heptadienal, as well as tridecanal were tested on early and later larval development in the sea urchin Paracentrotus lividus. We also tested the effect of some of the more abundant diatom polyunsaturated fatty acids (PUFAs) on development, in particular 5,8,11,14,17-eicosapentaenoic acid (EPA), one of the main precursors of diatom PUAs, as well as 4,7,10,13,16,19-docosahexaenoic acid (DHA), 6,9,12,15-octadecatetraenoic acid (stearidonic acid), 6,9,12-octadecatrienoic acid (γ-linolenic acid) and 9,12-octadecadienoic acid (linoleic acid). PUAs blocked sea urchin cell cleavage in a dose dependent manner and with increasing chain length from C7 to C10 PUAs, with arrest occurring at 27.27 µM with heptadienal, 16.13 µM with octadienal, 11.47 µM with octatrienal and 5.26 mM with decadienal. Of the PUFAs tested, only EPA and stearidonic acid blocked cleavage, but at much higher concentrations compared to PUAs (331 μM for EPA and 181 μM for stearidonic acid). Sub-lethal concentrations of decadienal (1.32–5.26 μM) delayed development of embryos and larvae which showed various degrees of malformations depending on the concentrations tested. Sub-lethal concentrations also increased the proportion of TUNEL-positive cells indicating imminent death in embryos and larvae. Using decadienal as a model PUA, we show that this aldehyde can be detected spectrophotometrically for up to 14 days in f/2 medium.</description>
	
	<guid>http://www.mdpi.com/1660-3397/8/4/950/</guid>
	<pubDate>Tue, 30 Mar 2010 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2010-03-30</prism:publicationDate>
	<prism:volume>8</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>950</prism:startingPage>
		<prism:endingPage>967</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>Teratogenic Effects of Diatom Metabolites on Sea Urchin Paracentrotus lividus Embryos</dc:title>
	<dc:date>2010-03-30</dc:date>
	<dc:identifier>doi: 10.3390/md8040950</dc:identifier>
		<dc:creator> Romano</dc:creator>
		<dc:creator> Miralto</dc:creator>
		<dc:creator> Ianora</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1660-3397/8/4/881/">
	<title>Marine Drugs, Vol. 8, Pages 881-915: Impact of Marine Drugs on Cytoskeleton-Mediated Reproductive Events</title>
	<link>http://www.mdpi.com/1660-3397/8/4/881/</link>
	<description>Marine organisms represent an important source of novel bioactive compounds, often showing unique modes of action. Such drugs may be useful tools to study complex processes such as reproduction; which is characterized by many crucial steps that start at gamete maturation and activation and virtually end at the first developmental stages. During these processes cytoskeletal elements such as microfilaments and microtubules play a key-role. In this review we describe: (i) the involvement of such structures in both cellular and in vitro processes; (ii) the toxins that target the cytoskeletal elements and dynamics; (iii) the main steps of reproduction and the marine drugs that interfere with these cytoskeleton-mediated processes. We show that marine drugs, acting on microfilaments and microtubules, exert a wide range of impacts on reproductive events including sperm maturation and motility, oocyte maturation, fertilization, and early embryo development.</description>
	
	<guid>http://www.mdpi.com/1660-3397/8/4/881/</guid>
	<pubDate>Thu, 25 Mar 2010 00:00:00 CET</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2010-03-25</prism:publicationDate>
	<prism:volume>8</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>881</prism:startingPage>
		<prism:endingPage>915</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>Impact of Marine Drugs on Cytoskeleton-Mediated Reproductive Events</dc:title>
	<dc:date>2010-03-25</dc:date>
	<dc:identifier>doi: 10.3390/md8040881</dc:identifier>
		<dc:creator> Silvestre</dc:creator>
		<dc:creator> Tosti</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1660-3397/8/3/471/">
	<title>Marine Drugs, Vol. 8, Pages 471-482: Primary Screening of the Bioactivity of Brackishwater Cyanobacteria: Toxicity of Crude Extracts to Artemia salina Larvae and Paracentrotus lividus Embryos</title>
	<link>http://www.mdpi.com/1660-3397/8/3/471/</link>
	<description>Cyanobacteria are a diverse group of Gram-negative bacteria that produce an array of secondary compounds with selective bioactivity against vertebrates, invertebrates, plants, microalgae, fungi, bacteria, viruses and cell lines. The aim of this study was to assess the toxic effects of aqueous, methanolic and hexane crude extracts of benthic and picoplanktonic cyanobacteria isolated from estuarine environments, towards the nauplii of the brine shrimp Artemia salina and embryos of the sea urchin Paracentrotus lividus. The A. salina lethality test was used as a frontline screen and then complemented by the more specific sea urchin embryo-larval assay. Eighteen cyanobacterial isolates, belonging to the genera Cyanobium, Leptolyngbya, Microcoleus, Phormidium, Nodularia, Nostoc and Synechocystis, were tested. Aqueous extracts of cyanobacteria strains showed potent toxicity against A. salina, whereas in P. lividus, methanolic and aqueous extracts showed embryo toxicity, with clear effects on development during early stages. The results suggest that the brackishwater cyanobacteria are producers of bioactive compounds with toxicological effects that may interfere with the dynamics of invertebrate populations.</description>
	
	<guid>http://www.mdpi.com/1660-3397/8/3/471/</guid>
	<pubDate>Fri, 05 Mar 2010 00:00:00 CET</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2010-03-05</prism:publicationDate>
	<prism:volume>8</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>471</prism:startingPage>
		<prism:endingPage>482</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>Primary Screening of the Bioactivity of Brackishwater Cyanobacteria: Toxicity of Crude Extracts to Artemia salina Larvae and Paracentrotus lividus Embryos</dc:title>
	<dc:date>2010-03-05</dc:date>
	<dc:identifier>doi: 10.3390/md8030471</dc:identifier>
		<dc:creator>Viviana R. Lopes</dc:creator>
		<dc:creator>Nuria Fernández</dc:creator>
		<dc:creator>Rosário F. Martins</dc:creator>
		<dc:creator>Vitor Vasconcelos</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1660-3397/8/1/59/">
	<title>Marine Drugs, Vol. 8, Pages 59-79: Effects of Marine Toxins on the Reproduction and Early Stages Development of Aquatic Organisms</title>
	<link>http://www.mdpi.com/1660-3397/8/1/59/</link>
	<description>Marine organisms, and specially phytoplankton species, are able to produce a diverse array of toxic compounds that are not yet fully understood in terms of their main targets and biological function. Toxins such as saxitoxins, tetrodotoxin, palytoxin, nodularin, okadaic acid, domoic acid, may be produced in large amounts by dinoflagellates, cyanobacteria, bacteria and diatoms and accumulate in vectors that transfer the toxin along food chains. These may affect top predator organisms, including human populations, leading in some cases to death. Nevertheless, these toxins may also affect the reproduction of aquatic organisms that may be in contact with the toxins, either by decreasing the amount or quality of gametes or by affecting embryonic development. Adults of some species may be insensitive to toxins but early stages are more prone to intoxication because they lack effective enzymatic systems to detoxify the toxins and are more exposed to the toxins due to a higher metabolic growth rate. In this paper we review the current knowledge on the effects of some of the most common marine toxins on the reproduction and development of early stages of some organisms.</description>
	
	<guid>http://www.mdpi.com/1660-3397/8/1/59/</guid>
	<pubDate>Tue, 19 Jan 2010 00:00:00 CET</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2010-01-19</prism:publicationDate>
	<prism:volume>8</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>59</prism:startingPage>
		<prism:endingPage>79</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>Effects of Marine Toxins on the Reproduction and Early Stages Development of Aquatic Organisms</dc:title>
	<dc:date>2010-01-19</dc:date>
	<dc:identifier>doi: 10.3390/md8010059</dc:identifier>
		<dc:creator>Vítor Vasconcelos</dc:creator>
		<dc:creator>Joana Azevedo</dc:creator>
		<dc:creator>Marisa Silva</dc:creator>
		<dc:creator>Vítor Ramos</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1660-3397/7/3/367/">
	<title>Marine Drugs, Vol. 7, Pages 367-400: The Influence of Bioactive Oxylipins from Marine Diatoms on Invertebrate Reproduction and Development</title>
	<link>http://www.mdpi.com/1660-3397/7/3/367/</link>
	<description>Diatoms are one of the main primary producers in aquatic ecosystems and occupy a vital link in the transfer of photosynthetically-fixed carbon through aquatic food webs. Diatoms produce an array of biologically-active metabolites, many of which have been attributed as a form of chemical defence and may offer potential as candidate marine drugs. Of considerable interest are molecules belonging to the oxylipin family which are broadly disruptive to reproductive and developmental processes. The range of reproductive impacts includes; oocyte maturation; sperm motility; fertilization; embryogenesis and larval competence. Much of the observed bioactivity may be ascribed to disruption of intracellular calcium signalling, induction of cytoskeletal instability and promotion of apoptotic pathways. From an ecological perspective, the primary interest in diatom-oxylipins is in relation to the potential impact on energy flow in planktonic systems whereby the reproductive success of copepods (the main grazers of diatoms) is compromised. Much data exists providing evidence for and against diatom reproductive effects; however detailed knowledge of the physiological and molecular processes involved remains poor. This paper provides a review of the current state of knowledge of the mechanistic impacts of diatom-oxylipins on marine invertebrate reproduction and development.</description>
	
	<guid>http://www.mdpi.com/1660-3397/7/3/367/</guid>
	<pubDate>Fri, 21 Aug 2009 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Marine Drugs</prism:publicationName>
	<prism:publicationDate>2009-08-21</prism:publicationDate>
	<prism:volume>7</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>367</prism:startingPage>
		<prism:endingPage>400</prism:endingPage>
		<prism:issn>1660-3397</prism:issn>
	
	<dc:title>The Influence of Bioactive Oxylipins from Marine Diatoms on Invertebrate Reproduction and Development</dc:title>
	<dc:date>2009-08-21</dc:date>
	<dc:identifier>doi: 10.3390/md7030367</dc:identifier>
		<dc:creator>Gary  S. Caldwell</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>


<cc:License rdf:about="http://creativecommons.org/licenses/by/3.0/">
	<cc:permits rdf:resource="http://creativecommons.org/ns#Reproduction" />
	<cc:permits rdf:resource="http://creativecommons.org/ns#Distribution" />
	<cc:permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks" />
</cc:License>

</rdf:RDF>
