Metazoan parasite assemblages of wild Seriola lalandi (Carangidae) from eastern and southern Australia

Yellowtail kingfish, Seriola lalandi support significant commercial and recreational fisheries as well as aquaculture operations throughout the world. Metazoan parasite infections of S. lalandi are of considerable economic and ecological importance, yet very little is known about wild parasite assemblages. S. lalandi were collected from the east coast and south coast of Australia and examined for metazoan parasites. Forty-three parasite taxa were identified, including 26 new host records. Four of the parasite species recovered have been previously associated with disease or mortality in Seriola aquaculture. Comparisons are made between ectoparasite and endoparasite prevalence and intensity of S. lalandi from New South Wales and Victoria. S. lalandi sampled from the east coast of Australia shared ectoparasites previously documented from this species in New Zealand, providing support that S. lalandi in the Tasman Sea comprise a single stock. Based on previously used criteria to evaluate the suitability of parasites as biological tags, the monogenean Paramicrocotyloides reticularis Rohde and the copepod Parabrachiella seriolae Yamaguti and Yamasu may be potentially useful for stock discrimination.     

N',2-diphenylquinoline-4-carbohydrazide based NK3 receptor antagonists II

Introduction of selected amine containing side chains into the 3-position of N',2-diphenylquinoline-4-carbohydrazide based NK3 antagonists abolishes unwanted hPXR activation. Introduction of a fluorine at the 8-position is necessary to minimize unwanted hI(Kr) affinity and a piperazine N-tert-butyl group is necessary for metabolic stability. The lead compound (8m) occupies receptors within the CNS following oral dosing (Occ(90) 7 mg/kg po; plasma Occ(90) 0.4 microM) and has good selectivity and excellent PK properties.     

Neonatal mouse gonocyte proliferation assayed by an in vitro clonogenic method

Survival and proliferation of mouse gonocytes was studied using a single cell clonogenic assay in vitro. The effect of growth factors and extracellular matrix on clonogenic development was quantitated. Fundamental requirements for growth of neonatal gonocytes included addition of fetal calf serum and coating culture wells with collagen IV alone or with added fibronectin. After 4-5 days, colonies ranged in size from four to > 128 cells, and some contained very elongated cells indicating migratory behaviour. Soluble stem cell factor did not have any effect on clonogenicity, although STO (subline of SIM mouse fibroblasts) cells, which produce membrane-bound stem cell factor, reduced colony formation from 79 +/- 5.9% to 20 +/- 3.3% without added growth factor. The majority of gonocytes and type A spermatogonia express the c-kit receptor according to in situ hybridization studies. However, the results indicate that the receptor may not be functional in neonatal gonocytes and their immediate progeny. The current assay for gonocytes can be extended to test new growth factors or proliferation-inducing agents directly, as well as to study cell-cell interactions. This assay and long-term propagation of neonatal germ cells will provide the much needed resources to enable greater understanding of the early development of germ cells.