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122 records · Page 7Linked to original sources
PubMed1998

Influences of caloric restriction on age-associated skeletal muscle fiber characteristics and mitochondrial changes in rats and mice.

The effect of caloric restriction (CR) initiated in adult rats (17 months of age) on the abundance of deleted mitochondrial genomes, mitochondrial enzymatic abnormalities, and fiber number was examined in rat skeletal muscle. Vastus lateralis muscle from young (3-4 months) ad libitum-fed, old (30-32 months) restricted (35% and 50% CR, designated CR35 and CR50, respectively), and old ad libitum-fed rats (29 months) was studied. CR preserved fiber number and fiber-type composition in the CR50 rats. In the old rats from all groups, individual fibers were found with either no detectable cytochrome-c oxidase activity (COX-), hyperactive for succinate dehydrogenase activity (SDH++), or both COX- and SDH++. Muscle from the CR50 rats contained significantly fewer COX- and SDH++ fibers than did the muscle from the CR35 rats. CR50 rats also had significantly lower numbers of mtDNA deletion products in two (adductor longus and soleus) of the four muscles examined compared to CR35 rats. These data indicate that CR begun in late middle age can retard age-associated fiber loss and fiber-type changes as well as lower the number of skeletal muscle fibers exhibiting mitochondrial enzyme abnormalities. CR can also decrease the accumulation of deleted mitochondrial genomes.

Aging↗
PubMed2001

Detection and analysis of depolarization artifacts in rotating-compensator polarimeters.

Absolute constraints, namely, the Schwarz inequality and a complementary expression derived by us, are used to obtain corresponding absolute constraints on the Fourier coefficients of the intensity transmitted through rotating-compensator polarimeters and ellipsometers. These expressions allow the investigation of artifacts that result in mixed or apparently mixed polarization states over the cross section of the beam, the averaging time of the detector, or the frequency passband of the dispersing element. Examples include multiple internal reflections or inhomogeneous strain within an element, scattered light, and other types of system and component defects that cannot be accessed by means of polarization-state data alone. We apply these results to our polarizer-sample-compensator-analyzer (PSCA) ellipsometer to illustrate capabilities. A simple analytic model is shown to give a quantitative description of depolarization in systems for which the resolution is finite and the retardation varies with wavelength.

Journal Article↗
PubMed2004

Optimizing precision of rotating-analyzer and rotating-compensator ellipsometers.

I investigate the dependence of shot-noise-limited uncertainties of the ellipsometric parameters psi, and delta for the rotating-analyzer ellipsometer (RAE) and the rotating-compensator ellipsometer (RCE) of the polarizer-sample-compensator-analyzer type. The development is general and takes into account correlations among the Fourier coefficients of the transmitted intensity, in particular the average intensity, which is necessarily correlated with all other coefficients through normalization. The results are expressed in terms of the traditional uncertainties delta(psi) and delta(delta) of the ellipsometric parameters psi and delta, respectively, although a more appropriate measure of uncertainty is the differential area 2delta(psi) x sin psi(delta)delta on the unit-radius Poincaré sphere. Numerical results for broadband operation from 1.5 to 6.0 eV with a Si sample show that the optimum measurement conditions for both configurations occur when the intensity of light reflected from the sample is approximately balanced between the TE and the TM modes, and, for the RCE, when the analyzer azimuth is essentially equal to that of the polarizer. Under typical broadband operating conditions in which components cannot be optimized on a wavelength-by-wavelength basis, the RCE is better at determining delta, whereas the RAE is better at determining psi. The approach is easily generalized to other configurations and other types of experimental uncertainty, both random and systematic.

Journal Article↗
PubMed1976

Clinical effects and pharmacokinetics of different dosage schedules of adriamycin.

Adriamycin was administered to 60 adults and 21 children by 3 different dosage schedules: 22.5 mg/sq m (0.6 mg/kg) daily for 4 days, 15 mg/sq m (0.4 mg/kg) every 8 hr for a total of 6 doses, and 50 to 120 mg/sq m as a single dose every 3 to 4 weeks. Objective responses lasting more than 1 month occurred in 5 subjects with acute leukemias or lymphoma, 3 with transitional cell carcinomas, 2 with sarcomas, 2 with Ewing's sarcoma and 1 each with bronchogenic carcinoma, orchidoblastoma, and thymoma. Toxic reactions included nausea, vomiting, stomatitis, alopecia, and hematopoietic depression, but significant cardiac toxicity occurred in only 1 patient. Pharmacokinetic data, collected in 25 patients by fluorometric and chromatographic assay, suggested a biphasic plasma clearance of drug with initial and secondary half-lives of about 1.5 and 14 to 21 hr, respectively. When drug was given every 8 hr there was evidence of loss of an initial very rapid phase of distribution of adriamycin and its metabolites. Urinary excretion accounted for 3.4 to 38.1% of administered fluorescence over a 72-hr period; in the first 24 hr, between 48.2 and 100% of this urinary material was in the form of adriamycin; leter, this fraction declined. No adriamycin or its fluorescent metabolites could be extracted from the stools.

Blood Cells↗