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1.
Front Microbiol ; 9: 355, 2018.
Article in English | MEDLINE | ID: mdl-29545783

ABSTRACT

At the mouth of the Amazon River, a widespread carbonate ecosystem exists below the river plume, generating a hard-bottom reef (∼9500 km2) that includes mainly large sponges but also rhodolith beds. The mesozooplankton associated with the pelagic realm over the reef formation was characterized, considering the estuarine plume and oceanic influence. Vertical hauls were carried out using a standard plankton net with 200 µm mesh size during September 2014. An indicator index was applied to express species importance as ecological indicators in community. Information on functional traits was gathered for the most abundant copepod species. Overall, 179 zooplankton taxa were recorded. Copepods were the richest (92 species), most diverse and most abundant group, whereas meroplankton were rare and less abundant. Species diversity (>3.0 bits.ind-1) and evenness (>0.6) were high, indicating a complex community. Small holoplanktonic species dominated the zooplankton, and the total density varied from 107.98 ind. m-3 over the reef area to 2,609.24 ind. m-3 in the estuarine plume, with a significant difference between coastal and oceanic areas. The most abundant copepods were the coastal species ithona plumifera and Clausocalanus furcatus and early stages copepodites of Paracalanidae. The holoplanktonic Oikopleura, an important producer of mucous houses, was very abundant on the reefs. The indicator species index revealed three groups: (1) indicative of coastal waters under the influence of the estuarine plume [Euterpina acutifrons, Parvocalanus crassirostris, Oikopleura (Vexillaria) dioica and Hydromedusae]; (2) characterized coastal and oceanic conditions (Clausocalanus); (3) characterized the reef system (O. plumifera). Two major copepods functional groups were identified and sorted according to their trophic strategy and coastal-oceanic distribution. The species that dominated the coastal area and the area over the rhodolith beds are indicators of the estuarine plume and are mixed with species of the North Brazil Current. These species practically disappear offshore, where occur oceanic species commonly found in other oligotrophic tropical areas. This ecosystem shows a mixture of estuarine, coastal and oceanic communities coexisting in the waters over the Amazon reefs, with no significant differences among these areas. However, the MDS clearly separated the communities along the salinity gradient in the plume.

2.
J Endocrinol ; 158(3): 295-303, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9846158

ABSTRACT

Chronic exposure of sheep adipose tissue to growth hormone (GH) in vitro decreases the ability of the adenosine analogue, N6-phenylisopropyladenosine (PIA), to inhibit isoprenaline-stimulated lipolysis by a mechanism which is dependent on both gene transcription and protein serine/threonine phosphorylation. The inhibition is not due to a change in ligand binding to the adenosine receptor, the amounts of the three isoforms of the inhibitory GTP-binding protein, Gi, or the maximum (forskolin-stimulated) adenylate cyclase activity. The ability of GH to modulate the PIA-activated adenosine receptor to stimulate dissociation of heterotrimeric Gi was assessed by measurement of pertussis toxin-catalysed ADP-ribosylation of Gi; GH does not appear to alter the interaction between the activated receptor and Gi. The ability of GH to alter the ability of activated Gi to inhibit adenylate cyclase activity was assessed by measuring the ability of a GTP analogue, guanosine 5'-[beta gamma-imido]triphosphate (p[NH]ppG), to inhibit forskolin-stimulated adenylate cyclase activity; chronic exposure to GH prevented this effect of p[NH]ppG. Thus the attenuation of the inhibition of lipolysis by PIA by chronic exposure of adipocytes to GH appears to be due to an impairment in the interaction between adenylate cyclase and the alpha subunit of one or more isoforms of Gi.


Subject(s)
Adipocytes/metabolism , GTP-Binding Proteins/metabolism , Growth Hormone/pharmacology , Lipolysis/drug effects , Phenylisopropyladenosine/pharmacology , Receptors, Purinergic P1/drug effects , 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/pharmacology , Adenosine Diphosphate Ribose/metabolism , Adenylate Cyclase Toxin , Adenylyl Cyclases/metabolism , Adipocytes/drug effects , Adrenergic beta-Agonists/pharmacology , Analysis of Variance , Animals , Cell Membrane/metabolism , Colforsin/pharmacology , Culture Techniques , Enzyme Inhibitors/pharmacology , Guanylyl Imidodiphosphate/pharmacology , Isomerism , Isoproterenol/pharmacology , Male , Models, Biological , Okadaic Acid/pharmacology , Pertussis Toxin , Protein Binding , Sheep , Stimulation, Chemical , Virulence Factors, Bordetella/pharmacology
3.
J Anim Sci ; 74(3): 562-8, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8707711

ABSTRACT

The basis of the chronic lipolytic effect of somatotropin on adipose tissue was investigated in sheep. Lipolytic rate was assessed in subcutaneous adipose tissue both in vivo, by microdialysis, and in vitro. Somatotropin treatment resulted in a small increase in basal (unstimulated) lipolysis and also in the maximum lipolytic rate observed in the presence of catecholamines both in vivo and in vitro. There was a small increase in the number of beta-adrenergic receptors but no change in the amount of the two isoforms of the stimulatory GTP-binding protein, Gs. Treatment with somatotropin decreased the response to antilipolytic agents such as the adenosine analog N6-phenylisopropyladenosine and prostaglandin E1. There was, however, no change in the number of adenosine receptors or amounts of the inhibitory GTP-binding proteins (Gi-1 plus Gi-2). Somatotropin also decreased prostaglandin E2 production by subcutaneous adipose tissue in vivo. Somatotropin treatment thus alters lipolytic regulation in sheep and this is characterized by changes in a number of proteins involved in this process.


Subject(s)
Adipose Tissue/metabolism , Growth Hormone/pharmacology , Lipolysis/drug effects , Sheep/metabolism , Adipocytes/chemistry , Adipocytes/ultrastructure , Adipose Tissue/chemistry , Adipose Tissue/ultrastructure , Animals , Catecholamines/pharmacology , Cell Membrane/chemistry , Cell Membrane/ultrastructure , Female , GTP-Binding Proteins/analysis , GTP-Binding Proteins/chemistry , GTP-Binding Proteins/metabolism , Glycerol/blood , In Vitro Techniques , Isomerism , Lipolysis/physiology , Receptors, Adrenergic, alpha/analysis , Receptors, Adrenergic, alpha/drug effects , Receptors, Adrenergic, alpha/metabolism , Receptors, Adrenergic, beta/analysis , Receptors, Adrenergic, beta/drug effects , Receptors, Adrenergic, beta/metabolism , Sheep/physiology
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