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Biomedical subjects

P A Schenck

Publications and source records attributed to P A Schenck.

6 recordsLinked to original sources
PubMed1996

Delta 8 desaturation in vivo of deuterated eicosatrienoic acid by mouse liver.

In vitro evidence has been reported for an alternate pathway that involves delta 8 desaturation of n-6 and n-3 polyunsaturated fatty acids (PUFA). The present study was designed to allow detection of delta 8 desaturation in vivo and to provide an estimation of the relative contribution of delta 8 desaturation to the in vivo synthesis of n-3 fatty acids. Male adult ICR mice were fed a semisynthetic fat-free diet for eight days, and then the diets were supplemented for three days with deuterated 11,14,17-eicosatrienoic acid (20:3-d8) labeled at the 3,3,4,4,8,8,9,9 carbon positions. Analysis of liver total lipid by gas chromatography/mass spectroscopy indicates that the total deuterated fatty acids contained 22.3% 20:3n-3-d8 and 28.9% of metabolites formed by elongation and delta 5 desaturation of 20:3n-3-d8. Deuterated metabolites resulting from retroconversion to 18:3-d6 and subsequent metabolism by classical pathways represented 35.3% of the total deuterated fatty acids. The retroconversion product (18:4n-3-d6) of 20:4n-3-d6 and/or -d8 was 9.0% of the total. A minor percentage (4.4%) of the products identified (20:4n-3-d6, 20:5n-3-d6, 22:5n-3-d6, 22:6n-3-d5 and 24:6n-3-d5) were formed by delta 8 desaturation. This study provides the first clear evidence of delta 8 desaturation in vivo in the mouse liver. Whether delta 8 desaturation would have a greater importance in vivo when the delta 6 desaturase pathway is disrupted remains to be determined.

Animals↗
PubMed1996

Fractionation of canine serum calcium, using a micropartition system.

OBJECTIVE: To determine usefulness of a micropartition system for calcium fractionation of canine serum, and to establish reference values for protein-bound, complexed, and ionized calcium fractions in clinically normal dogs. DESIGN: Performance characteristics of a micropartition system were evaluated, using serum from clinically normal dogs. This micropartition system was then used to determine a reference range for calcium fractions. ANIMALS: 13 clinically normal dogs. PROCEDURE: Dog serum was placed in the micropartition system, and spun for 20 minutes at 1,300 x g. Total calcium concentration, ionized calcium concentration, and pH were measured in whole serum, and total calcium concentration was measured in the ultrafiltrate. The protein-bound fraction was calculated by subtracting total calcium of the ultrafiltrate from total calcium of whole serum. The ionized calcium measurement of whole serum was subtracted from the total calcium measurement of the ultrafiltrate, determining the complexed calcium fraction. RESULTS: During validation of the ability of the micropartition system to separate calcium fractions, no significant amount of serum calcium was adsorbed by the plastic micropartition system or membrane. The micropartition membrane separated the protein-bound calcium fraction (retentate) from the ultrafiltrate, which contained ionized and complexed fractions of calcium. Concentrations of protein-bound, ionized, and complexed calcium from clinically normal dogs were determined to be 3.40 +/- 0.63, 5.49 +/- 0.17, and 1.01 +/- 0.30 mg/dl, representing 34, 56, and 10% of the total calcium concentration, respectively. CONCLUSIONS: This method is a rapid, repeatable means to completely fractionate serum calcium, and most importantly provides accurate assessment of the protein-bound and complexed calcium fractions. CLINICAL RELEVANCE: Complete assessment of calcium fractions may increase sensitivity for detection of disease processes that affect calcium metabolism.

Analysis of Variance↗
PubMed1995

Effects of storage on serum ionized calcium and pH values in clinically normal dogs.

The stability of ionized calcium (CaI) concentration and pH in sera (n = 14) stored at 23 or 4 C for 6, 9, 12, 24, 48, or 72 hours, or -10 C for 1, 3, 7, 14, or 30 days was evaluated. Also studied were the effects of oxygen exposure, cold handling, and feeding on CaI and pH values. Results indicated that serum CaI concentration was stable throughout 72 hours of storage at 23 or 4 C, and for 7 days at -10 C. Serum CaI concentration significantly (P < 0.05) decreased by 14 days of storage at -10 C. Serum pH was stable for 6 hours at 23 or 4 C, and for 24 hours at -10 C, but significantly (P < 0.05) increased by 9 hours of storage at 23 or 4 C and by 3 days at -10 C. Exposure of the surface of the serum to air immediately before measurement had no effect on CaI or pH values, but mixing serum with air resulted in significantly (P < 0.05) decreased CaI concentration and increased pH. Handling of blood on ice resulted in significantly (P < 0.05) higher serum pH, compared with blood handled at 23 C, but serum CaI concentration was unaffected. Serum obtained at 2 hours after feeding did not have any significant changes in CaI, total calcium, or pH values. It appears that if canine serum is obtained, handled, and stored anaerobically, CaI concentration can be accurately measured after 72 hours at 23 or 4 C, or after 7 days at -10 C.

Animals↗
PubMed1989

Nutritional management of hepatic disease.

The successful management of hepatic diseases of dogs and cats requires an understanding of hepatic metabolism and nutritional processes. General aspects of dietary therapy for hepatic diseases are described, along with specific recommendations for the promotion of tissue regeneration. Special considerations, including the role of diet in encephalopathy, hepatic lipidosis, and copper-associated hepatic toxicosis, are also discussed.

Animals↗
PubMed1987

Effect of body weight on osteopenia in ovariectomized rats.

Bilateral ovariectomies or sham surgeries were performed in female Sprague Dawley rats that were 78 days of age and weighed an average of 210 g. Food was available ad libitum to the control rats and to a group of ovariectomized rats (obese OVX). The food consumption of a second group of ovariectomized rats (weight-matched OVX) was restricted to match their body weights to those of the control rats. All rats were sacrificed at 14 weeks postovariectomy. Radioimmunoassay of terminal serum estradiol confirmed the success of ovariectomy. The estradiol concentration in control rats was 24.9 +/- 20.2 pg/ml, whereas the hormone was undetectable (less than 10 pg/ml) in both groups of OVX rats. The final body weights of control and weight-matched OVX rats were nearly identical (approximately 260 g). In contrast, obese OVX rats weighed significantly more than both of the above groups (approximately 320 g, P less than 0.001). The proximal tibia and lumbar vertebra were processed undecalcified for quantitative bone histomorphometry. Tibial trabecular bone volume (TBV) was determined to be 17.6 +/- 4.5%, 7.9 +/- 5.3%, and 3.6 +/- 3.1% for the control, obese OVX, and weight-matched OVX groups, respectively. Tibial TBV for both OVX groups was significantly less than the control value (P less than 0.001). The difference in tibial TBV between obese OVX and weight-matched OVX rats was also statistically significant (P less than 0.02). Histologic indices of bone resorption and formation were indicative of increased bone turnover in the proximal tibia of both OVX groups.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗