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J R Powell

Publications and source records attributed to J R Powell.

At least 217 records · Page 12Linked to original sources
PubMed1972

Allozymes as diagnostic characters of sibling species of Drosophila.

Considerable enzyme variation that is genetically controlled exists within and between natural populations of Drosophila. Our studies of two groups of sibling species show that allozyme differences can be used as species-diagnostic characters. A locus is defined as diagnostic if an individual can be correctly assigned to one of two species with a probability of 99% or higher. Between 15 and 32% of the loci studied are diagnostic for any two of the sibling species. If several diagnostic loci are used, the species of any individual can be diagnosed with virtual certainty.

Acid Phosphatase↗
PubMed1972

Enzyme variability in the Drosophila willistoni group. IV. Genic variation in natural populations of Drosophila willistoni.

We describe allelic variation at 28 gene loci in natural populations of D. willistoni. Seventy samples were studied from localities extending from Mexico and Florida, through Central America, the West Indies, and tropical South America, down to South Brazil. At least several hundred, and often several thousand, genomes were sampled for each locus. We have discovered a great deal of genetic variation. On the average, 58% loci are polymorphic in a given population. (A locus is considered polymorphic when the frequency of the most common allele is no greater than 0.95). An individual fly is heterozygous, on the average, at 18.4% loci.-Concerning the pattern of the variation, the most remarkable finding is the similarity of the configuration of allelic frequencies from locality to locality throughout the distribution of the species. Our observations support the conclusion that balancing natural selection is the major factor responsible for the considerable genetic variation observed in D. willistoni.

Alleles↗
PubMed1972

Antacids.

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Antacids↗
PubMed1971

Genetic polymorphisms in varied environments.

Thirteen experimenital populationis of Drosophila willistoni were maintained in cages, in some of which the environments were relatively constant and in others varied. After 45 weeks, the populations were assayed by gel electrophoresis for polymorphisms at 22 protein loci. The average heterozygosity per individual and the average unmber of alleles per locus were higher in populations maintained in heterogeneous environments than in populations in more constant enviroments.

Alleles↗
PubMed1971

Polymorphisms in continental and island populations of Drosophila willistoni.

A comparative study of genic allozyme and chromosomal polymorphisms in four continental (South American) and six oceanic island (West Indies) populations of Drosophila willistoni has been made. The pattern of genic polymorphism is closely similar in all populations. Although regional and local differences in gene frequencies are found, generally the same alleles occur at high, intermediate, and low frequencies in all populations. An average individual is heterozygous at 18.4 and 16.2% of its loci in the continental and island populations, respectively. By contrast, chromosomal polymorphism is sharply reduced on the islands compared to most continental populations, and some chromosomal inversions are more frequent on some islands than on others. The observations are not compatible with the hypothesis that most of the gene variants are adaptively neutral. Balancing natural selection is responsible for most of the genic polymorphism in natural populations of D. willistoni.

Alleles↗
PubMed1970

Evidence of heterosis associated with an enzyme locus in a natural population of Drosophila.

A wild population of Drosophila paulistorum (Andean semispecies) was analyzed by starch gel electrophoresis for a sex-linked enzyme locus, Tetrazolium oxidase. The results of the analysis of F(1) progenies from 106 single female lines from São José do Rio Prêto, Brazil, has allowed us to determine the genotype of 106 wild-collected females and 104 wild-collected males. The population is polymorphic for two alleles with frequencies of 0.56 and 0.44. The observed frequencies among the females of the two homozygotes were 0.23 and 0.13 and of the heterozygote 0.64. The deviation from the frequencies expected according to the Hardy-Weinberg formula is statistically significant (P < 0.005). There is a substantial excess of heterozygotes over the expected number. This observation is interpreted to mean that this polymorphism is maintained by heterosis. This is probably the first reported case of heterosis associated with an enzyme locus in a natural population of Drosophila.

Animals↗
PubMedDate not supplied

Phenobarbital pharmacokinetics and bioavailability in adults.

The pharmacokinetics and bioavailability of phenobarbital were examined in six healthy adult subjects after a 2.6 mg/kg intravenous and a 2.9 mg/kg oral dose. Serum concentrations of phenobarbital were followed by means of a high pressure liquid chromatographic assay for 21 days after drug administration. After the intravenous dose, the mean distribution half-life was 0.18 hour and the mean elimination half-life was 5.8 days. Mean total body clearance and mean renal clearance were 3.0 ml/hr/kg and 0.8 ml/hr/kg, respectively. The apparent volume of distribution was 0.60 liter/kg. After administration of phenobarbital tablets, the maximum phenobarbital serum concentration was 5.5 mg/liter at 2.3 hours after the dose. Adjusted absolute availability of phenobarbital from the tablets studied was 94.9 per cent (range 81-111.9 per cent). The elimination half-life averaged 5.1 days for the oral dose. There was no evidence of autoinduction of phenobarbital elimination over the study period.

Adult↗
PubMedDate not supplied

The influence of H2-receptor antagonists on steady-state concentrations of propranolol and 4-hydroxypropranolol.

Twelve healthy male volunteers were treated with 1200 mg/day cimetidine, 300 mg/day ranitidine, or no H2-receptor antagonist (control) for seven days in a sequence determined by Latin-square design. Each treatment period was separated by a seven-day washout. On the third day of each treatment period, 80 mg propranolol every 12 hours for nine doses was initiated. Whole blood concentrations of propranolol and 4-hydroxypropranolol were measured at 12 time points during the 12-hour period following administration of the last propranolol dose. Heart rate was measured before each blood sample was withdrawn. Cimetidine treatment was associated with a 47 per cent increase in the area under the propranolol concentration-time curve and a 17 per cent increase in elimination half-life of propranolol. Ranitidine had no significant effect on the concentration-time profile of propranolol. There were no significant differences in the 4-hydroxypropranolol pharmacokinetic parameters during any of the treatments. There was, however, a significant decrease in the average 4-hydroxypropranolol-to-propranolol steady-state concentration ratio during the cimetidine treatment. There was no significant difference in heart rate between any of the treatments. The elevation of propranolol concentrations during cimetidine treatment is likely due to metabolic inhibition by cimetidine.

Adult↗
PubMedDate not supplied

Lack of effect of histamine H2-receptor antagonists on indocyanine green disposition measured by two methods.

Eleven healthy male volunteers were treated according to a randomized, crossover design with ranitidine (300 mg/day), cimetidine (1200 mg/day), or nothing for 48 hours. Ninety minutes after the 48-hour dose, each volunteer was given 0.5 mg/kg indocyanine green by iv bolus. Indocyanine green plasma concentrations were measured by the traditional spectrophotometric method at 800 nm and by HPLC simultaneously monitored at 214 and 656 nm. Neither histamine H2-receptor antagonist altered the disposition of indocyanine green. The mean (+/- S.D.) plasma clearance by the spectrophotometric method was 7.48 +/- 2.07 (control), 7.15 +/- 3.07 (ranitidine), and 6.88 +/- 1.35 ml/min/kg (cimetidine). The power to detect a 20 per cent change is 0.87. The spectrophotometric method generally produced a biexponential plasma concentration decay, whereas the HPLC method resulted in a monoexponential decay. Analysis of the 5- to 15-minute data by the conventional technique showed that although indocyanine green total plasma clearance was not significantly different for the two methods (P greater than 0.10), the volume of distribution was significantly greater (P less than 0.001) and the elimination rate constant was significantly smaller (P less than 0.001) for the spectrophotometric than the HPLC method. Although neither ranitidine nor cimetidine chronic administration alters indocyanine green disposition by either method, the absolute values of the pharmacokinetic parameters are dependent upon the analytical technique employed.

Adult↗