An experiment was conducted in 1995 in order to examine muscle growth, muscle histochemical properties, muscle metabolism and meat quality of two types of Danish Landrace pigs representing the growth potential of years 1976 and 1995, respectively. Danish Landrace pigs representing 1976 (slow-growing, SG) originated from a breeding station where the population was maintained without being selected for production traits such as daily gain, food conversion ratio and meat content. Pigs representing Danish Landrace of 1995 (fast-growing, FG) were bought from certified Danish pig breeders. The pigs were simultaneously tested for performance from 40 to 95 kg live weight. The daily gain, food conversion ratio and meat content of the carcass were improved proportionately by 0·43, 0·24 and 0·03 in FG pigs compared with SG pigs. In m. longissimus dorsi (LD), the cross-sectional area of muscle fibres was smaller in FG pigs compared with SG pigs indicating increased muscle fibre number. Data further suggest increased satellite cell proliferation in muscles of FG pigs. Serum from FG pigs stimulated the proliferation of C2C12 muscle cells to a greater extent than serum from SG pigs, although the serum level of insulin-like growth factor 1 did not differ between pig types. The effect of serum on protein turn-over of C2C12 myotubes did not depend on pig type. The glycogen concentration in the LD did not differ significantly between pig types, while the activity of citrate synthase, 3-OH-acyl-CoA-dehydrogenase, and lactate dehydrogenase were higher in the LD of SG pigs compared with FG pigs. Pork chop colour of FG pigs was proportionately 0·09 lighter (L⋆) and 0·13 less red (a⋆) than pork chops of SG pigs. The total muscle pigment concentration in the LD, m. biceps femoris and m. vastus intermedius was proportionately reduced by 0·17, 0·19 and 0·11, respectively, in FG pigs compared with SG pigs. In the LD, the concentration of myoglobin was proportionately reduced by 0·17 in FG pigs. The chemical composition of the LD differed between pig types such that the water content was higher and protein content lower in LD from FG pigs compared with SG pigs. The pH of the LD measured 45 min and 24 h post mortem, drip loss and thawing loss were similar for both pig types. Meat tenderness of conditioned pork chops of FG pigs was slightly reduced in accordance with a decreased intensity of the 31 kDa peptide band and increased cooking loss. The present study suggests that increased muscle fibre number and rate of muscle DNA deposition (satellite cell proliferation) have contributed to the increased muscle growth as a result of selection for performance in pigs under Danish conditions. However, the increase in growth performance was accompanied by deterioration in muscle colour and slightly reduced tenderness.
Antibody-capture enzyme-linked immunosorbent assay (ELISA) using enzyme-labeled cytomegalovirus (CMV) nuclear antigen is a reliable and easily performed test suitable for routine use. As the serologic response to CMV infection may, however, vary considerably among patients, we have studied the kinetics of CMV-specific immunoglobulin M (IgM), IgE, IgA, and IgG antibodies in 352 sera from 61 patients by using antibody-capture ELISA and complement fixation (CF) tests. In a CMV mononucleosis group (n = 17), most patients had antibodies of all four immunoglobulin classes, but antibody levels decreased rapidly, with half the patients having a borderline-positive or a negative reaction for all classes, except IgG, 2 months after the appearance of symptoms. Twelve patients with a primary CMV infection after renal or bone marrow transplantation also developed all immunoglobulin-class antibodies. In only two patients did CMV IgM and IgE antibodies precede seroconversion of CF antibodies, and in one patient, these antibodies lagged months behind. Most patients had all classes of CMV antibodies, except IgA, for a year or more. Among 10 transplant patients with a secondary CMV infection, 50% had long-lasting IgM antibodies, and very few had IgE or IgA antibodies, but all had IgG antibodies to CMV. In 13 infected infants, the CMV-specific serologic response was also characterized by long-lasting IgM, IgE, and IgG antibodies. Two patients did not develop detectable IgM antibodies, and one of these did not show IgE antibodies either. The IgA response in infants as a whole was * Corresponding author.
The present experiment was undertaken to study the transcription of members of the insulin-like growth factor (IGF) system and myostatin in porcine satellite cells through myogenesis and to study the effects of 1 µmol/L insulin on stimulating fusion. Cultured cells were harvested at 50 and 80% confluence and at days 1, 2, 3 and 4 following induction of fusion and differentiation. Increased levels of myogenin transcription and creatine kinase from 50% confluence until day 2 indicated that fusion and differentiation were induced. The mRNA abundance of IGF-I (P < 0.001), IGF-II (P < 0.001), IGF binding protein (BP) 5 (P < 0.01), type I IGF receptor (P < 0.001) and myostatin (P < 0.01) increased from proliferation to differentiation. Insulin stimulated differentiation as indicated by elevated creatine kinase activity (P < 0.001) but did not affect myogenin mRNA abundance (P = 0.98). Insulin downregulated transcription of IGF-I (P < 0.01) and during the first 2 days after switching to differentiation medium insulin downregulated IGF receptor transcription (P < 0.001), whereas insulin did not affect transcription of IGF-II (P = 0.06), IGFBP5 (P = 0.76) or myostatin (P = 0.50). In conclusion, transcriptions of IGF-I, IGF-II, type I IGF receptor, IGFBP5 and myostatin were changed during myogenesis, suggesting autocrine/ paracrine roles in regulating the transition from proliferation to differentiation of porcine satellite cells.
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