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Biomedical subjects

L A Kuehn

Publications and source records attributed to L A Kuehn.

At least 19 recordsLinked to original sources

Genetic (co)variance components for ewe productivity traits in Katahdin sheep.

The objective of this study was to estimate genetic parameters, in Katahdin sheep, for total weight of litter weaned per ewe lambing (TW) and its components, number of lambs born (NB), number of lambs weaned (NW), and average weight of lambs weaned (AW) measured as traits of the ewe. Weaning weights of lambs (WW) were adjusted to 60 d of age and for effects of ewe age, lamb sex, and type of birth and rearing and averaged over all lambs in the litter to obtain AW. The 60-d age-adjusted WW were adjusted for ewe age and lamb sex and summed over all lambs in the litter to obtain TW. A total of 2,995 NB and NW records, 2,622 AW, and 2,714 TW records were available from 1,549 ewes (progeny of 235 sires) over 4 yr. Heritabilities were initially estimated for each trait from univariate REML analyses. Estimates of genetic correlations were obtained from bi- and trivariate analyses. Models for NB, NW, AW, and TW included random ewe additive and permanent environmental effects. A random service sire effect was also fit for AW and TW. Heritabilities of TW, NB, NW, and AW from univariate analyses were 0.12, 0.12, 0.09, and 0.13 (all P < 0.01), respectively. Permanent environmental effects were significant (P < 0.01) for TW and AW. Genetic correlations of TW with NB, NW, and AW ranged from 0.27 to 0.33, 0.88 to 0.91, and 0.72 to 0.76, respectively; those of NB with NW and AW ranged from 0.70 to 0.75 and -0.01 to 0.02, respectively; and that between NW and AW ranged from 0.40 to 0.55. Genetic parameters were also obtained for lamb survival to weaning (LS) and WW measured as traits of the lamb, and the relationships between WW of the ewe as a lamb and her subsequent records for NB and NW were also estimated. A total of 5,107 LS and 5,444 WW records were available. Models for WW and LS included random animal and maternal genetic, maternal permanent environmental, and litter effects. Heritability of WW ranged from 0.15 to 0.20. There was no evidence of genetic effects on LS. Direct genetic correlations of WW with NB and NW were not significantly different from zero. The correlation between maternal genetic effects on WW, and animal genetic effects on NW, averaged 0.35. Results of this study indicate that there are no major antagonisms among TW and its components, so that selection for TW would not have adverse effects on any component traits and vice versa. Maternally superior ewes for WW appear to also be somewhat superior for NW.

Animals↗

Association of a single nucleotide polymorphism in SPP1 with growth traits and twinning in a cattle population selected for twinning rate.

Continued validation of genetic markers for economically important traits is crucial to establishing marker-assisted selection as a tool in the cattle industry. The objective of the current study was to evaluate the association of a SNP (T(9)/T(10)) in the osteopontin gene (SPP1) with growth rate in a large cattle population spanning multiple generations and representing alleles from 12 founding breeds. This population has been maintained at the US Meat Animal Research Center since 1981 and subjected to selection for twinning rate. Phenotypic records for this population included twinning rate and ovulation rate, providing an opportunity to examine the potential effects of SPP1 genotype on reproductive traits. A set of 2,701 animals was geno-typed for the T(9)/T(10) polymorphism at SPP1. The geno-typic data, including previously genotyped markers on chromosome 6 (BTA6), were used in conjunction with pedigree information to estimate genotypic probabilities for all 14,714 animals with phenotypic records. The genotypic probabilities for females were used to calculate independent variables for regressions of additive, dominance, and imprinting effects. Genotypic regressions were fit as fixed effects in a mixed model analysis, in which each trait was analyzed in a 2-trait model where single births were treated as a separate trait from twin births. The association of the SPP1 marker with birth weight (P < 0.006), weaning weight (P < 0.007), and yearling weight (P < 0.003) was consistent with the previously reported effects of SPP1 genotype on yearling weight. Our data supports the conclusion that the SNP successfully tracks functional alleles affecting growth in cattle. The previously undetected effect of the SNP on birth and weaning weight suggests this particular SPP1 marker may explain a portion of the phenotypic variance explained by QTL for birth and HCW on BTA6.

Animals↗

Antibody response of chickens to sheep red blood cells: crosses among divergently selected lines and relaxed sublines.

Crosses were made among lines of chickens that had undergone 30 generations of selection for high or low antibody response 5 d after an intravenous injection with SRBC, and between sublines in which selection was relaxed in generation 24. Antibody responses at 5, 10, and 14 d after injection were measured in the 4 lines and in reciprocal crosses among them. Divergence between the high and low lines selected for SRBC antibody was immediate and increased during selection. Although significant in both cases, separation of the relaxed subline from its respective selected line was greater in the high than the low line. Five-day SRBC titers of the relaxed lines and the crosses were intermediate to the high and low selected lines, with the direction and magnitude of heterosis being line dependent. A high proportion of chickens from low line mating combinations did not have detectable antibody titers at 10 and 14 d postinoculation with SRBC, precluding statistical analysis of these data. Results are discussed in the context of intra- and interlocus effects on the selected trait.

Animals↗

Response to intensity of reproduction in mouse lines resistant or susceptible to fescue toxicosis.

Our objective was to examine whether mouse lines divergently selected for response to fescue toxicosis differed in the impact of increasing reproductive intensity on growth, final weight or first and second parity reproduction. Resistant (R) and susceptible (S) females were never mated (NR), mated only once (low reproduction, LR), mated after their first litter was weaned (moderate reproduction, MR) or paired continuously with a male (high reproduction, HR), allowing concurrent pregnancy and lactation. Final weight was significantly higher in mated than in not mated females (31.6 +/- 0.6, 35.9 +/- 0.6, 36.8 +/- 0.6 and 37.2 +/- 0.5 g for NR, LR, MR and HR females respectively), but the effect of increasing reproductive intensity was similar in both lines. Neither genetic line, reproductive treatment (LR and MR versus HR) nor their interaction affected first parity traits of dams or pups. In second parity, S dams produced larger litters at birth and weaning and heavier litters at birth than R dams, and MR dams produced more pups and heavier litters than HR dams. As with first litters, however, line by reproductive treatment interactions were not significant or important. Concurrent pregnancy and lactation (the HR treatment) had a similar dampening impact on the expected increase in litter size between first and second parity of both lines. Thus, lines divergently selected for toxicosis response did not differ significantly in the impact of increasing reproductive intensity on dam or pup growth, reproductive output through two parities or mature size. This conclusion should not be generalized. Selection responses in livestock should be monitored to ensure that improvement in one trait does not lead to deterioration in others.

Animals↗

Sleep time following anesthesia in mouse lines selected for resistance or susceptibility to fescue toxicosis.

In previous work, a mouse line selected for resistance (R) to fescue toxicosis had higher activities of two hepatic Phase II detoxification enzymes than a mouse line selected for fescue toxicosis susceptibility (S). The primary objective of the present study was to determine whether those same lines also differed in hepatic Phase I enzyme activity, estimated from sleep time (ST) following sodium pentobarbital anesthesia. Additional objectives were to determine whether ST differences between lines were modulated by endophyte-infected fescue in the diet (with or without an enzyme inducer) and whether ST of individual mice was correlated with the effect of a toxin-containing diet on the postweaning growth of those mice. In Exp. I, 24 males from each line were randomly assigned to each of five diets: control (commercial rodent food meal); E+ (50% endophyte-infected fescue seed, 50% control); E+P (the E+ diet supplemented with 1,000 ppm phenobarbital); E- (50% endophyte-free fescue seed, 50% control); and E-P (the E- diet supplemented with 1,000 ppm phenobarbital). After 4 wk on these diets, ST was measured on all the mice. A second ST was recorded on each mouse by randomly sampling one-fourth of the population after 1, 2, 3, or 4 wk on a pelleted rodent food diet. Regardless of diet, R mice had shorter first and second ST than S mice (P < 0.01), suggesting higher hepatic Phase I microsomal enzyme activity. Mice on both phenobarbital-supplemented diets had shorter first ST than mice whose diets did not include that microsomal enzyme inducer (P < 0.01). In Exp. II, ST was measured on male and female R and S mice (n = 280) after they had been fed the E- diet for 2 wk, then the E+ diet for 2 wk, and then a pelleted rodent food diet for 2 wk. Growth response to the E+ diet was the percentage of reduction in gain on the E+ diet compared to gain on the E- diet the previous 2 wk. As in Exp. I, S mice slept longer than R mice (P < 0.01). The residual correlation between ST and gain reduction associated with the E+ diet equaled 0.04. Thus, an animal's apparent Phase I enzyme activity did not predict its growth rate depression on the toxin-containing diet. Based on these and previous studies, divergent selection for toxicosis response in mice was successful partially by causing divergence in activities of hepatic Phase I and II detoxification enzymes.

Acremonium↗

The effect of alcohol on body heat loss.

The effect of the ingestion of alcohol on cooling in seminude human subjects was examined at 25 and 30 degrees C in air; in heavily clothed individuals at -23 degrees C in air; and nude subjects in a water calorimeter at 25 degrees C. It was observed that consumption of the equivalent of five bar whiskey drinks did not affect the cooling rate of subjects as measured by infrared techniques or by thermistors. Total heat loss, measured in the calorimeter, was also not affected by drinking alcohol. It is concluded that the ingestion of alcohol does not cause an increase in cooling rate in humans.

Adult↗

Body cooling after death.

In the analyses of cases of death in cold air environments, it is often of interest to determine the time required for the body of the individual to cool to ambient temperature. Usually such determinations have been based on Newton's law of cooling. This paper describes a case history in which this technique was experimentally tested and consequently abandoned in favour of a more complex biophysical model which more accurately described the thermo-physical events inherent in body cooling. This model is recommended for determination of the times required for various body parts to cool to ambient environmental temperatures.

Animals↗

Similarity in the number of lifespan heartbeats among non-hibernating homeothermic animals.

An investigation was made of the available data on heart rates and maximum lifespan of a number of vertebrates from a variety of sources; only data pertinent to resting adult non-anesthesized homeothermic mammals and birds in a state of thermal neutrality were subsequently analyzed. All known hibernators were excluded because of their extreme, and largely unknown, range of heartbeat from season to season. Plots of heart rate (beats per minute) against reciprocal of lifespan in years showed surprisingly good fits (r = +0.90 for mammals and r = +0.64 for birds). Computation of the total number of heartbeats in the maximum recorded lifespans of the mammalian and avian species involved in this study showed that the mean cumulative heartbeat number for 31 mammalian species was 100 +/- 8 S.E.M. x 10(7) beats and for 23 avian species was 326 +/- 22 S.E.M. x 10(7) beats. This paper documents this analysis, which supports the concept of a close similarity in lifespan heartbeats among mammalian species and among avian species.

Animals↗

Thermal measurements on divers in hyperbaric helium-oxygen environments.

During a series of three saturation dives to simulated depths of 1000, 1200, and 1400 fsw at the Ocean Simulation Facility, measurements were made to establish the rate of heat loss of unclad divers in helium-oxygen gaseous environments. These measurements were part of a program to determine the dangers of cold stress and the temperature/time relationship tolerated by divers in cold diving bells or in hyperbaric chambers in which environmental conditions are uncontrolled. Three specific gaseous temperatures of 15, 20, and 25 degrees C were considered. In each experiment, as many as four subjects were monitored for body core and mean skin temperature over a 2-h testing period. One or two of the subjects were also monitored for mean body convective heat loss to determine physiological (shell) thermal insulation. Results of these experiments are expressed in depth-time-temperature three-dimensional graphs in whic, the temperature variable is one of the following: mean skin temperature change, mean body temperature change, or mean rectal (core) temperature change, each suitable for defining diver thermal limitations. It was also possible to rank body areas of the subjects in relation to heat loss and temperature decrease during exposure to the cold environment.

Adult↗

Effects on handgrip strength due to arm immersion in a 10 degree C water bath.

Thirteen male and female human subjects participated in an experiment to determine if cold water immersion of the arm increases post-immersion handgrip strength. The test involved immersion of a subject's fore-arm into a 10 degrees C water bath for 30 min once a week in a 3-week series, involving a control test and two immersion experiments. Handgrip strength was measured 20 min before and then once every 20 minutes after the cold bath immersion for 4 h, for a total of 18 readings. Grip strength significantly decreased as a consequence of immersion of the forearm. However, strength recovery to approximately normal values took place within 40 min. No increases in post-immersion strength were observed.

Adult↗

Survival test of submersible life support systems.

An experiment to validate predictions concerning submersible survivability was performed in December, 1975, by members of the Canadian Forces in the CF Submersible Lockout Vehicle SDL-1 in Halifax Harbour in water of 4 degrees C temperature at a depth of 40 ft. Data was collected relevant to the life support equipment to determine if it would operate for a simulated 6-h mission followed by a 24-h immobility period, at the end of which rescue was presumed to have occurred. Physiological data was collected from the submersible occupants in order to assess the degree of thermal stress experienced in this exercise. The experiment was terminated after a duration of approximately 25 h at 1 atm internal pressure due to exhaustion of two of the three on-board power supplies, causing the CO2 scrubbers to be inoperative and the CO2 content in the breathing gas to increase to toxic levels. Only two of the three submersible occupants experienced cold stress, one in the forward sphere and one in the aft sphere. At the end of 24 h, the core temperatures of both individuals had decreased by 0.5 degrees C and, during this time, skin temperatures, particularly of the extremities, had steadily and slowly decreased. Neither individual was hypothermic, but it was considered likely that after a 3-d exposure, at least two of the crew members would have had core temperatures of 35 degrees C or lower, assuming that CO2 poisoning had not occurred earlier.

Air↗