Behavioral studies indicate a right hemisphere advantage for processing a face as a whole and a left hemisphere superiority for processing based on face features. The present PET study identifies the anatomical localization of these effects in well-defined regions of the middle fusiform gyri of both hemispheres. The right middle fusiform gyrus, previously described as a face-specific region, was found to be more activated when matching whole faces than face parts whereas this pattern of activity was reversed in the left homologous region. These lateralized differences appeared to be specific to faces since control objects processed either as wholes or parts did not induce any change of activity within these regions. This double dissociation between two modes of face processing brings new evidence regarding the lateralized localization of face individualization mechanisms in the human brain.

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The objectives of this study were to determine the extent of changes in concentrations of testosterone, growth hormone (GH) and insulin-like growth factor I (IGF-I) concentrations in blood plasma and to characterize the respective plasma-binding proteins of these two peptides during the onset of puberty in male calves. The jugular veins of six male Holstein calves (11-weeks-old) were catheterized and blood was collected every 3 days (one sample every 30 min for 8 h). Hormone concentrations in plasma were determined by specific radioimmunoassay. After incubation with [125I]IGF-I, IGF-I-binding proteins (IGFBPs) were separated by gel filtration; radioactivity was determined in each fraction. Western ligand blotting using radiolabelled hormones as ligand was also used to characterize the IGF-I- and GH-binding proteins in plasma. Puberty was characterized by a rapid (in 1 or 2 days) increase in mean concentrations of testosterone in plasma (from 0.5 to > 2 ng ml-1) and a pulsatile release of the hormone. During puberty, IGF-I concentrations also increased rapidly in 8-10 days from +/- 50 ng ml-1 to > 150 ng ml-1, whereas concentrations of GH in plasma remained relatively stable during the experimental period. A significant correlation was observed between IGF-I and testosterone concentrations (r = 0.77; P < 0.001) throughout the experimental period. Three different IGF-I-binding protein fractions with apparent molecular masses of > 200, 150-170 and 45-65 kDa were found in plasma using gel filtration.(ABSTRACT TRUNCATED AT 250 WORDS)

Growth-promoters are banned by the European Community, but different hormonal cocktails are still illegally used. This experiment was therefore conducted to evaluate the effects of one of the most currently used cocktails on some hormonal parameters and spermatogenesis in finishing bulls in an attempt to provide a suitable screening technique for their illegal use. Sixteen double-muscled Belgian White Blue finishing bulls (mean ivcight: 535 (s.d. 37) kg) were blocked into control (C; no. = 7) and treated (Dex; no. = 9) groups. Animals were treated i.m. with the hormonal preparation (dexamethasone isonicotinate and phosphate, chlormadinone acetate and ethinyl oestradiol) on day 0, day 15 and day 30. Animals were slaughtered on day 45. Three h before each treatment and just prior to slaughter, jugular blood samples were collected to monitor the testosterone (T) response to an i.v. injection of gonadotropin releasing hormone (GnRH) (0·5 fig GnRH per kg body weight). Testicular tissue was also collected at slaughter. Plasma T and insulin-like growth factor-1 (IGF-1) concentrations were measured by radioimmunoassay. IGF-binding proteins (IGFBPs) were evaluated using Western ligand blotting. Daily weight gains were lower in the control group (1·29 (s.d. 0·13) kg for C v. 1·60 (s.d. 0·39) kg for Dex) but the difference ivas not significant. After treatment, spermatogonia, spermatocytes, spermatids and spermatozoa disappeared from the testis and seminiferous tubules consisted only of Sertoli cells; these observations suggest that treated animals were sterile. Moreover, plasma T concentrations in response to GnRH stimulation were suppressed fP < 0·001) in the Dex group between day 15 and day 45 (mean maximal responses: 5·4 to 7·9 μg/l in C group v. < 0·2 μg/l in Dex group at day 15, 30 and 45). Treatment did not show any prominent effect on plasma IGF-1 levels but increased IGFBPS band intensity. In conclusion, treatment with a cocktail containing dexamethasone esters, chlormadinone acetate and ethinyl oestradiol for a short period induced a number of changes in finishing bulls luhich might be possible to develop as a screening method for the identification of illegally treated animals.

The presence of GH-binding proteins (GHBPs) in the plasma of adult cattle was investigated using Sephadex G-200 filtration, Western ligand blotting and Western blotting. The changes in the concentration of GHBP in the plasma of dairy half-sister heifers during the first year of life as well as the presence of GHBP in milk were also investigated. When analytical chromatography (on a 1.6 x 100 cm column) was performed, five peaks of recombinant bovine GH (rbGH)-associated radioactivity were revealed in cattle plasma; the first peak, which appeared near the void volume, was presumed to represent aggregates, the second (M(r) 290 kDa) and the third peaks (M(r) 75 kDa) corresponded to specific rbGH-GHBP complexes; the last two peaks representing free 125I-labelled rbGH and Na[125I]. Western ligand blotting revealed multiple GHBPs. Three major bands were observed at approximately 190, 58 and 31 kDa; an excess of unlabelled hormone blocked the binding of 125I-labelled rbGH. Minor non-specific binding bands were also detected in cattle plasma with molecular weights between 40 and 136 kDa. One monoclonal antibody (8H7) produced against synthetic peptide (amino acids 54-63 of the extracellular domain of the bovine GH receptor) specifically interacted with 190 and 58 kDa bands while the 31 kDa band was not recognized. Finally, Western ligand blots were performed to evaluate the changes in plasma GHBP during the first year of life in 55 dairy half-sister heifers and to identify GHBP in milk. In plasma, the intensity of the 31 kDa band varied greatly between animals while the other specific bands remained stable.(ABSTRACT TRUNCATED AT 250 WORDS)