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Biomedical subjects

B L Hughes

Publications and source records attributed to B L Hughes.

At least 19 recordsLinked to original sources
PubMed1999

Rotations of a helix as a model for correction of the scoliotic spine.

STUDY DESIGN: A prospective study using intraoperative stereophotogrammetry to analyze helical motion of the spine during the correction of scoliosis. OBJECTIVE: To determine whether derotation systems rotate the scoliotic helix. SUMMARY OF BACKGROUND DATA: Scoliosis is a complex three-dimensional deformity that is difficult to visualize on standard radiographs. The use of stereophotogrammetry has allowed study of the deformity in three dimensions during surgical correction. METHODS: Thirty-five patients with right thoracic adolescent idiopathic scoliosis were studied using a stereophotogrammetry technique during surgical correction. Changes in vertebral unique rotations and spinal plane of maximum deformity were measured during three sequential stages of the surgery. RESULTS: The mean preoperative and postoperative Cobb angles were 58 degrees and 19 degrees, respectively. Most rotation occurred at the top and bottom vertebrae in the curve, averaging 10 degrees each but in opposite directions. The apical vertebra rotated the least in the structural curve, with an average rotation of 5 degrees. Much of the rotation occurred during the derotation maneuver with additional rotation occurring during the final distraction. The plane of maximum deformity changed from a mean of 50 degrees before instrumentation to 19 degrees at the end of the procedure. CONCLUSIONS: Multiple rotations of the scoliotic curve occur, and it can be shown when maximum rotations occur during surgery. Posterior derotational systems unwind or rotate the scoliotic helix and reposition the resultant sine wave toward the sagittal plane as described by the change in the plane of maximum deformity.

Adolescent↗
PubMed1998

Alanine, not ammonia, is excreted from N2-fixing soybean nodule bacteroids.

Symbiotic nitrogen fixation, the process whereby nitrogen-fixing bacteria enter into associations with plants, provides the major source of nitrogen for the biosphere. Nitrogenase, a bacterial enzyme, catalyzes the reduction of atmospheric dinitrogen to ammonium. In rhizobia-leguminous plant symbioses, the current model of nitrogen transfer from the symbiotic form of the bacteria, called a bacteroid, to the plant is that nitrogenase-generated ammonia diffuses across the bacteroid membrane and is assimilated into amino acids outside of the bacteroid. We purified soybean nodule bacteroids by a procedure that removed contaminating plant proteins and found that alanine was the major nitrogen-containing compound excreted. Bacteroids incubated in the presence of 15N2 excreted alanine highly enriched in 15N. The ammonium in these assays neither accumulated significantly nor was enriched in 15N. The results demonstrate that a transport mechanism rather than diffusion functions at this critical step of nitrogen transfer from the bacteroids to the plant host. Alanine may serve only as a transport species, but this would permit physiological separation of the transport of fixed nitrogen from other nitrogen metabolic functions commonly mediated through glutamate.

Journal Article↗
PubMed1996

Immunogenicity of tissue plasminogen activators in rhesus monkeys: antibody formation and effects on blood level and enzymatic activity.

The immunogenicity of a tissue-type plasminogen activator analog, mt-PA6, consisting of the second kringle and protease domains, was compared to that of the native-sequence protein (nt-PA) in rhesus monkeys. Antibody responses were compared in groups of eight monkeys that were treated by i.v. injection twice, 1 month apart, using doses and regimens chosen to mimic therapy (0.5 mg/kg mt-PA6 bolus, 1.25 mg/kg nt-PA bolus + infusion). An additional group was treated with a 0.5 mg/kg nt-PA bolus. A single positive response was obtained in a monkey treated with 0.5 mg/kg nt-PA after the primary injection. Following the secondary injection, responses were obtained in 1/8, 3/8, and 6/8 monkeys treated with mt-PA6, nt-PA as a bolus, or nt-PA as a bolus + infusion, respectively. Several monkeys were selected to determine whether circulating tPA antibody altered the pharmacokinetics of mt-PA6. Clearance was found to decrease without affecting peak blood levels as antibody concentrations increased from 0.02 to 100 micrograms/ml. In contrast, the peak blood level was reduced by 99% at an antibody concentration of 152 micrograms/ml in a monkey that had been exposed to mt-PA6 in adjuvant 14 months previously. Further, only the serum from this and three other hyperimmunized monkeys inhibited the enzymatic activity of tPA in vitro. It is concluded that mt-PA6 is not more immunogenic than nt-PA in rhesus, and that low levels of antibody are more likely to influence the pharmacokinetic properties of tPA than to inhibit its enzymatic activity. It is unlikely that mt-PA6 would present a serious immunogenic risk in humans.

Animals↗
PubMed1994

Influence of amylase genotypes on growth rate and feed conversion of chickens.

Chickens from two breeds were screened for amylase alleles designated as AmyF and AmyS to establish breeder flocks homozygous for each. Offspring from these flocks were then used to test the hypothesis that AmyF and AmyS amylases differ in their ability to digest cornstarch and wheat starch. The amylase allozymes were found to affect growth and feed conversion performance of the chickens, and the effects were more pronounced in one breed. However, these effects seemed to be more related to specific activity of the amylases than to starch source in the diet. The results indicate that in some breeds of chickens selection for AmyS may improve growth and feed efficiency performance.

Alleles↗
PubMed1991

Effects of exposing broiler breeders to nicarbazin contaminated feed.

Ten-mo-old broiler feeds were fed nicarbazin (NCZ) at 0, 25, 50 and 100 ppm of their diet for 2, 4, or 6 days to simulate accidental contamination of their feed with the medicant. Reduced egg production was observed in all treatments except 25 and 50 ppm NCZ for 2 days. A consistent reduction in egg weight occurred only at the maximum treatment level of 100 ppm for 6 days. Reduction in hatchability was generally evident by Days 5 and 6 of the experiment except for the lowest treatment of 25 ppm NCZ for 2 days. Due partially to the low number of eggs set, no statistically significant reduction in hatchability was seen for the group receiving 50 ppm NCZ for 4 days, but hatchability had dropped over 17 percentage points (from 93.3 to 75.5%) by Days 5 and 6 of the experiment, and continued to drop to a low of 31% on Days 11 and 12 of the experiment. Shell pigmentation was the most sensitive characteristic measured, with significant depigmentation occurring after only 2 days of feeding 25 ppm NCZ. Generally, the severity and duration of effects were in proportion to medicant concentration and length of treatment time. Fertility was not influenced by the medicant.

Animal Feed↗
PubMed1990

The amylase gene-enzyme system of chickens. II. Biochemical characterization of allozymes.

The chicken amylase allozymes, AmyF and AmyS, were extracted from pancreatic tissues of AmyF/F and AmyS/S individuals and purified. Activities were measured under various reaction conditions (= treatments) to assess whether the allozymes were functionally different. The amylases had properties typical of alpha-amylases, i.e., both were inhibited by ethylenediaminetetraacetate and alpha-amylase inhibitor from wheat, had pH optima between 7.0 and 8.0, and could utilize a variety of substrates containing alpha 1,4 linkages. The amylases were also found to be inhibited by potassium phosphate buffer and p-chloromercuribenzoate. In terms of substrate specificity, both amylases could utilize all of the substrates tested with activity observed in the following order: amylopectin greater than potato starch greater than dextrin greater than glycogen greater than amylose. Statistical analysis indicated significant functional differences between the two allozymes in terms of specific activities, substrate specificities, and inhibitor sensitivities. AmyF had a significantly lower specific activity than did AmyS. The amylases responded differently to the substrate amylose, with AmyF better able to digest this substrate. AmyS was less sensitive than AmyF to alpha-amylase inhibitor from wheat.

Amylases↗
PubMed1990

Reproduction responses of broiler-breeders to anticoccidial agents.

Two experiments were conducted to determine the effects of anticoccidial agents on production and reproduction of broiler breeders. In Experiment 1, nicarbazin (NCZ) was fed at 20, 50, and 100 ppm. There was no depression in egg production, egg weight, or fertility from feeding these levels. As level of NCZ increased, there was a linear decrease in hatchability. The amount of 4,4'-dinitrocarbanilide (DNC) in the egg yolks increased linearly as the levels of NCZ went up; the degree of egg-shell depigmentation was directly related to the level of NCZ fed starting at 50 ppm. Experiment 2 utilized a different strain of broiler breeders. Halofuginone (3 ppm), maduramicin (5 ppm), monensin (100 ppm), narasin (70 ppm), NCZ (125 ppm), robenidine (33 ppm), and salinomycin (60 ppm) were fed to broiler breeders at the levels listed. Only NCZ reduced egg production. Narasin induced a reduction in egg weight. Both narasin and salinomycin caused a significant drop in hatchability. Feeding NCZ also induced a rapid and more severe decrease in hatchability. Monensin was the only anticoccidial agent that reduced fertility. Halofuginone, maduramicin, and robenidine had no biologically significant effect on henday production, egg weight, hatch of fertile eggs, or shell depigmentation. Feeding NCZ at 125 ppm caused a complete bleaching of brown-shell eggs by the 3rd consecutive day of treatment; but 7 days after NCZ was withdrawn from the feed, pigmentation returned to the pretreatment level.

Animals↗
PubMed1990

Production and egg-quality responses of White Leghorn layers to anticoccidial agents.

Two studies were conducted to determine the effects of anticoccidial agents on the production and reproduction of White Leghorns. In Experiment 1, nicarbazin (NCZ) was fed at 0, 20, 50, and 100 ppm. Hen-day egg production, egg weight, the egg-yolk DNC (4-4'-dinitrocarbanilide) level, and egg-yolk mottling were affected by the treatments. When response was evidenced, the relationship between those variables and the level of NCZ was basically linear. Decreased egg production occurred from Days 5 and 6 of the treatment through Days 1 and 2 of withdrawal. On Days 9 and 10 of treatment, the control hens peaked at 92% hen-day production, while hens fed 20, 50, and 100 ppm of NCZ peaked late--at 90, 82, and 80%, respectively. Compared to the controls, egg weight was reduced linearly as the level of dietary NCZ increased. The egg-yolk DNC level increased from Days 3 and 4 of treatment through Days 9 and 10 of withdrawal. Egg yolk mottling generally increased along with the level and duration of feeding NCZ. If the NCZ was mistakenly fed to White Leghorn layers, ill effects would be alleviated within 10 days after drug withdrawal. In Experiment 2, halofuginone (3 ppm), maduramicin (5 ppm), monensin (100 ppm), narasin (70 ppm), nicarbazin (125 ppm), robenidine (33 ppm), and salinomycin (60 ppm) were fed to White Leghorn hens at the levels specified in parentheses. Nicarbazin reduced egg production, depressed egg weight, reduced shell thickness, and caused egg-yolk mottling; but internal egg quality, as measured by Haugh Units, was unaffected. Halofuginone, maduramicin, monensin, narasin, robenidine, and salinomycin did not have a meaningful effect on the variables measured when fed to White Leghorn layers.

Animal Feed↗
PubMed1988

The amylase gene-enzyme system of chickens. I. Allozymic and activity variation.

Amylase allozymic and activity variation was studied in three flocks of chickens (Gallus domesticus). Individuals from one flock were studied to assess the effects of sex, tissue, and genotype on amylase activity. Additionally, the allozymes were purified and their specific activities compared. Variation was observed within and among the flocks. Two alleles were found to be segregating in the flocks, one flock being polymorphic and the other two monomorphic. Mean amylase activities among the three flocks were significantly different. The relationship of this activity variation to regulatory variation is discussed. There were no significant effects of sex or genotype on amylase activity and, in most cases, no correlation between activities in the various tissues. However, in heterozygotes one of the alloamylases had much lower activity than the other.

Amylases↗
PubMed1988

Comparison of primary rabbit kidney and MRC-5 cells and two stain procedures for herpes simplex virus detection by a shell vial centrifugation method.

By using a conventional tissue culture method as a standard, four shell vial centrifugation culture (SVC) formats were compared for herpes simplex virus (HSV) detection in 300 clinical samples. Both MRC-5 and primary rabbit kidney (PRK) cells were used in the conventional and SVC systems. In addition, both a direct monoclonal fluorescent antibody to HSV (MAb-FA; Syva Corporation, Palo Alto, Calif.) and an indirect HSV polyclonal antibody-horseradish peroxidase stain (poly-HRP; Difco Laboratories, Detroit, Mich.) were used to stain shell vials of both cell types. Conventional tubes were incubated for up to 7 days with daily examination for cytopathic effect, which was confirmed as HSV by staining with an MAb-FA. Shell vials were inoculated, centrifuged, incubated for 16 to 24 h, and stained directly with MAb-FA or indirectly with a poly-HRP stain. Of the 300 specimens examined, 82 (27%) were HSV positive by conventional tissue culture. PRK cells detected 81 (99%) positive specimens, compared with 74 (90%) specimens detected with MRC-5 cells. Of the 82 positive specimens by conventional culture, the SVC formats detected 68 by MRC-5 and MAb-FA, 74 by MRC-5 and poly-HRP, 64 by PRK and MAb-FA, and 77 by PRK and poly-HRP. Therefore, PRK stained by an indirect method with poly-HRP was the most sensitive of the SVC formats tested, detecting 94% of the positive specimens.

Animals↗
PubMed1986

Frequency and structure of macrophages and abnormal sperm cells in guinea fowl semen.

Semen from young and old guinea fowl was examined for macrophages and abnormal sperm cells. Large numbers of macrophages were found in the semen from both groups. However, there were significantly more abnormal sperm cells in the semen of the young males. The abnormal cells consisted of large coiled cells, bent spermatozoa, and round-headed cells. The predominant abnormality in the young males was bent sperm, although their semen also contained large round cells. The large round cells were identified as abnormal spermatids by electron microscopy and were more prominent in the older males. The abnormal spermatids were pleomorphic and exhibited various stages of intermediate and late spermatid development. The macrophages were activated cells that exhibited phagocytosis of large number of normal spermatozoa but were never observed to engulf abnormal cells. Their ultrastructure consisted of numerous lipid droplets, vesicles of ingested spermatozoa, lysosomal structures, residual bodies, and undigested remnants of spermatozoa. The presence of macrophages and abnormal spermatids in semen has been associated with lowered fertility in other species; thus, semen with exorbitant numbers of these cells should not be used for artificial insemination of the guinea fowl.

Acrosome↗
PubMed1986

Effects of temperature on reproduction in guinea fowl.

The effects of four temperature regimens on the onset and maintenance of semen and egg production, fertility, hatchability, and feed consumption by guinea fowl were examined. Temperatures of 26.7 and 21.1 C hastened the onset of egg and semen production in guinea fowl. However, egg and semen production rates of guineas exposed to ambient or 15.6 C minimum temperatures eventually increased to the level of those exposed to the higher temperatures. This suggests that it may be possible to initiate production by exposure to a warm environment and then reduce the environmental temperature after egg and semen production has been well established. There were no statistically significant differences in fertility or hatchability. Differences seen in feed conversion were mainly due to delayed onset of egg production in the lower temperature regimens. Thus, it appears that proper winter management of guinea breeders would involve exposure to a warm temperature for some period of time.

Animals↗
PubMed1985

High-density winter brooding in a solar facility.

Broilers were brooded under high-density and low ventilation conditions in a solar facility to 25 days of age and then moved to conventional facilities for growout. Nonstatistical comparisons were made on the performance of these birds to that of broilers grown under conventional conditions starting at day-old. Body weight differences during the brooding phase were primarily due to density with birds in the solar house weighing an average of 10.2% less than those brooded in a conventional house. Growth depression continued during the growing phase but was reduced in magnitude to 3% at Day 46. During the brooding phase no definite trends were seen with regard to effects of ventilation or density on feed conversion. Compared with conventionally-housed birds, feed conversion of the birds in the solar facility was slightly poorer at the end of the brooding period. This trend was reversed in the growing phase due to compensatory growth, giving the solar brooded birds an overall advantage at the end of the study. Mortality during the 46-day study was within the expected range for both the solar-brooded (3.1%) and conventionally-brooded (3.0%) birds. Energy consumption for supplemental heat and ventilation in the solar facility (.76 kWh/bird) was similar to that reported for energy efficient, environmentally-controlled houses and about half that for conventional facilities. Litter moisture in the solar facility was excessive due to the high bird density, low ventilation rates, and the use of a concrete slab floor.

Animal Feed↗
PubMed1984

Phospholipid and cholesterol profiles from chicken seminal components during in vitro storage at 5 C.

Two experiments were conducted with undiluted chicken semen to determine if fluctuations in endogenous phospholipids and cholesterol might relate to loss of fertilizing capacity which accompanies in vitro storage for 24 hr at 5 C. The following parameters were monitored quantitatively: individual seminal plasma and spermatozoal phospholipids, spermatozoal cholesterol to phospholipid molar ratios, and spermatozoal cholesterol mole percent. After storage for various periods, total lipids were extracted with chloroform:methanol (2:1, v/v). Total phospholipids were obtained by precipitation with cold acetone and further resolved into individual components by thin layer chromatography. All phospholipids and cholesterol were quantitated spectrophotometrically. Spermatozoal phospholipids, the spermatozoal molar ratio of cholesterol to phospholipid, and the spermatozoal mole percent of cholesterol remained essentially the same throughout the 24-hr storage period. Seminal plasma phosphatidylethanolamine also did not fluctuate significantly during the storage period. However, the phosphatidylcholine and the phosphatidylserine-inositol fractions from the seminal plasma appeared to increase with time.

Animals↗
PubMed1984

Catabolism of phospholipids by chicken seminal components after storage.

The possibility of an activation of chicken spermatozoal phospholipase A2 during in vitro storage of undiluted semen was investigated. After storage for periods up to 24 hr at 5 C, the ability of semen to catabolize added phosphatidylcholine labeled on the 2nd carbon of glycerol with 14C oleic acid was assessed. Neither spermatozoa nor plasma from undiluted chicken semen was found to be capable of catabolizing added 14C labeled phosphatidylcholine, regardless of the storage period. No enzyme activity was evident when fresh semen was incubated under various assay conditions to determine the influence of cholic acid, calcium, and the type of phospholipid substrate on phospholipase A2 activity. The influence of spermatozoal protease activation on phospholipase A2 activity from undiluted chicken semen and from Naja naja naja was also investigated and found to have no influence on phospholipase A2 activity.

Animals↗