Digestion of concentrates in sheep. 5. The effect of adding fish meal and urea together to cereal diets on protein digestion and utilization by young sheep.
Explore the source record for details and available documents.
SEARCH · Search PubMed
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
The B-cell mitogens LPS and lipoprotein stimulate 20-35 percent of all B cells in the spleen of 6- to 8-wk old C3H/Tif mice, as determined by limiting dilution analysis of precursors. Each reactive cell grows to a clone of IgM-secreting PFC, enumerated in a hemolytic plaque assay detecting all IgM secreting cells, regardless of v-region specificity. We have used these mitogens to reveal the total repertoire of Ig specificities produced by these mitogen-reactive B cells. We have determined in plaque assays with six different target erythrocytes the number of spleen cells limiting to one the number of mitogen-reactive B cells detected as specific IgM-secreting clones in each of these plaque assays. By this method, the absolute frequencies of precursor B cells with defined v-gene specificities could be calculated, for at least, one third of all B cells. The frequencies of specific IgM-plaque-forming B-cell clones within the total pool of mitogen-reactive B cells was 1 in 10 for NIP(12),-SRC, 1 in 50 for TNP(12)- SRC, 1 in 100 for NIP(1)-SRC, 1 in 160 for TNP(3)- SRC, 1 in 500 for HRC, and 1 in 1,000 for SRC. These frequencies were the same in the LPS- and in the lipoprotein-reactive B-cell population for TNP(30)- SRC and SRC.
Temporal patterns of SRBC antibody response after primary and secondary inoculations were measured in White Leghorn males from lines selected 24 generations for high (HA) or low (LA) 5-d antibody titers to an i.v. inoculation with 0.1 mL of a 0.25% suspension of SRBC. Primary i.v. inoculations were administered at 50 d of age as 0.1 mL of either 0.025 or 0.25% suspension of SRBC. Antibody levels of SRBC were measured 3, 5, 7, 9, 11, 13, and 20 d after inoculation. Also, IgG levels were measured on samples obtained 3, 7, 13, and 20 d after inoculation. At 70 d of age, half of the cockerels in each line-dosage subclass were given a booster inoculation of 0.1 mL of 0.25% SRBC. The SRBC antibody was measured 3, 6, 9, and 13 d later in chicks both receiving and not receiving the second inoculation. Patterns of antibody response to SRBC dosage differed according to line, resulting in interactions of line by dosage by day. Concentrations of IgG were greater for Line HA than for LA at 7 and 11 d after inoculation with SRBC but not at 3 and 20 d. Antibody responses to the booster inoculation differed between lines with a dosage effect present for LA but not for HA chicks. The greater anamnestic response observed in LA than in HA chicks is explained in the context of the resource allocation paradigm.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Animals adjust the time of year that they reproduce through their ability to perceive and respond to critical aspects of their environment, such as photoperiod, nutrition or the socio-sexual milieu, and their genotype determines the degree of response to each stimulus. Ultimately, information from environmental cues filters through to the GnRH neurones in the brain which are the primary regulator of fertility. Each of these cues has been studied in isolation and the mechanisms by which they affect GnRH secretion are now better, if not fully, understood. In the field, the brain centres that control GnRH must integrate information from all cues at any given time before 'formulating a reproductive decision'. In this review, the effect of this integration is illustrated by showing how the acute GnRH response to a nutritional signal can be modulated by genotype, photoperiod and social cues, to the point of being completely blocked under some circumstances. Candidate pathways that may mediate these modulatory effects at both the whole body and brain have been proposed, although none of these pathways are confirmed and some have not yet been studied. As a guide for further research, we propose a working model that integrates the inputs and explains the interactions between them.