Two genetic lines of barrows and gilt pigs with lean BW gain averages of 280 and 375 g/d were used to evaluate their macro- and micromineral contents at BW intervals from 20 to 125 kg of BW. The experiment was a 2 x 2 x 5 factorial arrangement of treatments (i.e., 2 sexes, 2 genetic lines, and 5 BW intervals) conducted in a completely randomized design in 6 replicates using a total of 120 pigs. Initially, 12 pigs (3 from each genetic line and sex) were killed, and then at approximately 25 kg of BW intervals to 125 kg. Pigs were fed vitamin and mineral fortified corn-soybean meal diets. At slaughter the total body (except digesta and blood) of each pig was ground and analyzed for their macro- and micromineral contents. The high-lean genetic line (P < 0.03) pigs and barrows (P < 0.01) reached their targeted BW an average 3 d earlier than the low-lean genetic line and gilts. Total macro- and micromineral contents increased as BW increased, generally in a linear or quadratic (P < 0.01) manner. There was an increasing difference between genetic lines in some minerals as BW increased. Total body Ca content was greater in the low-lean genetic line with increasing differences occurring as BW increased resulting in a BW x genetic line interaction (P < 0.05), whereas P was similar for both genetic lines. The quantity of K (P < 0.01) and S (P < 0.01) increased at a greater rate in the high-lean genetic line as BW increased, resulting in BW x genetic line interactions (P < 0.01). Body Cl (P < 0.01), Mg (P < 0.06), Mn (P < 0.05), Se (P < 0.01), and Zn (P < 0.01) were greater in the high-lean genetic. As BW increased, the Ca:P and the P:K ratios were increasingly greater (P < 0.01) in the low-lean genetic line, whereas the K:Na ratio was greater (P < 0.01) in high-lean genetic line. Although K and Fe were greater (P < 0.05) in gilts than in barrows, other mineral content differences were not significant. When minerals were expressed on a per kilogram of empty BW basis, the macro- and microminerals differed (P < 0.01) as BW increased indicating a response by body maturity. Genetic line had a greater effect on mineral content per kilogram of empty BW than sex. These results indicate that differences in mineral content are largely affected by BW or physiological age and by genetic line. Best-fitting equations were developed to determine macro- and micromineral contents of both genetic lines.

Download full-text PDF

Source
http://dx.doi.org/10.2527/jas.2006-545DOI Listing

Publication Analysis

Top Keywords

genetic lines
24
genetic
18
macro- micromineral
16
micromineral contents
16
high-lean genetic
16
low-lean genetic
12
mineral content
12
001
11
lines barrows
8
intervals 125
8

Similar Publications

An endoplasmic reticulum-localized Cu transporter, PhHMA5II1, interacts with copper chaperones and plays an important role in Cu detoxification in petunia. Copper (Cu) is an essential element for plant growth but toxic when present in excess. In this study we present the functional characterization of a petunia (Petunia hybrida) P-type heavy-metal ATPases (HMAs), PhHMA5II1.

View Article and Find Full Text PDF

The evolution of preferred male traits, female preference and the G matrix: "Toto, I've a feeling we're not in Kansas anymore".

Heredity (Edinb)

January 2025

Department of Evolution, Ecology and Organismal Biology, 2710 Life Science Bldg, University of California, Riverside, CA, 92521, USA.

Female preference exerts selection on male traits. How such preferences affect male traits, how female preferences change and the genetic correlation between male traits and female preference were examined by an experiment in which females were either mated to males they preferred (S lines) or to males chosen at random from the population (R lines). Female preference was predicted to increase the time spent calling by males.

View Article and Find Full Text PDF

Background: Mutations in the structural domain of the epidermal growth factor receptor (EGFR) kinase represent a critical pathogenetic factor in non-small cell lung cancer (NSCLC). Small-molecule EGFR-tyrosine kinase inhibitors (TKIs) serve as first-line therapeutic agents for the treatment of EGFR-mutated NSCLC. But the resistance mutations of EGFR restrict the clinical application of EGFR-TKIs.

View Article and Find Full Text PDF

HDAC and MEK inhibition synergistically suppresses HOXC6 and enhances PD-1 blockade efficacy in BRAF-mutant microsatellite stable colorectal cancer.

J Immunother Cancer

January 2025

Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Gastrointestinal Surgery III, Peking University Cancer Hospital & Institute, Beijing, China

Background: B-Raf proto-oncogene, serine/threonine kinase (BRAF)-mutant microsatellite stable (MSS) colorectal cancer (CRC) constitutes a distinct CRC subgroup, traditionally perceived as minimally responsive to standard therapies. Recent clinical attempts, such as BRAF inhibitors (BRAFi) monotherapy and combining BRAFi with other inhibitors, have yielded unsatisfactory efficacy. This study aims to identify a novel therapeutic strategy for this challenging subgroup.

View Article and Find Full Text PDF

MAF1 inhibits hepatocarcinogenesis by fostering an immunostimulatory tumor microenvironment.

J Immunother Cancer

January 2025

State Key Laboratory of Oncology in South China, and Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, China

Background: The biological significance of MAF1, a tumor suppressor, in carcinogenesis and immune response of hepatocellular carcinoma (HCC) remains unreported. Understanding the underlying mechanisms by which MAF1 enhances anti-tumor immunity in HCC is crucial for developing novel immunotherapy strategies and enhancing clinical responses to treatment for patients with HCC.

Methods: Mice were subjected to hydrodynamic tail vein injections of transposon vectors to overexpress AKT/NRas, or c-Myc, with or without wild-type (WT) or mutant-activated (-4A) MAF1, or short-hairpin MAF1 (shMAF1).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!