Accurate Chromatographic Method for Sorption Isotherms and Phase Equilibria

Partition coefficients can be determined with accuracy by a "tracerpulse" method in which the retention volume of a tracer of the respective species is measured. The method is applicable to multicomponent equilibria and can be used at elevated temperature and pressure. A less accurate "differential" method not requiring a tracer is also described.     

Serum thyroid hormone concentrations in clinically normal dogs after administration of freshly reconstituted vs previously frozen and stored thyrotropin

Concentrations of serum thyroxine (T4) and 3,3',5-triiodothyronine (T3) were determined in 7 clinically healthy adult dogs before and after administration of freshly reconstituted thyrotropin (TSH) and TSH that had been previously reconstituted and frozen for 1, 2, and 3 months. The 4 TSH response tests were performed at 30-day intervals by collecting blood samples for serum T4 and T3 determinations before and 4 and 6 hours after IV administration of TSH (0.1 U/kg of body weight). Baseline serum concentrations of T4 and T3 were similar at each of the 4 sample collection times over the 3-month period of the study. Mean serum concentrations of T4 and T3 increased significantly (P less than 0.01) over baseline values after administration of freshly reconstituted TSH or TSH that had been previously frozen for 1, 2, or 3 months. Significant difference was not found in the mean post-TSH serum T4 or T3 concentration after injection of freshly reconstituted TSH or TSH that had been previously frozen for 1, 2, or 3 months. In 2 of the 7 dogs, mild reactions--mild ataxia and weakness--were observed during the last of the series of TSH response tests (ie, after IV administration of TSH that had been previously frozen for 3 months). Results of this study suggest that for use in dogs, reconstituted TSH stored at -20 C maintains adequate biological activity for at least 3 months. The ability to store reconstituted TSH for a longer period than the recommended 48 hours represents an economic advantage, because it allows clinicians to perform more TSH response tests per vial of TSH.     

Primary Hypoadrenocorticism in Ten Cats

Primary hypoadrenocorticism was diagnosed in ten young to middle-aged cats of mixed breeding. Five of the cats were male, and five were female. Historic signs included lethargy (n = 10), anorexia (n = 10), weight loss (n = 9), vomiting (n = 4), and polyuria (n = 3). Dehydration (n = 9), hypothermia (n = 8), prolonged capillary refill time (n = 5), weak pulse (n = 5), collapse (n = 3), and sinus bradycardia (n = 2) were found on physical examination. Results of initial laboratory tests revealed anemia (n = 3), absolute lymphocytosis (n = 2), absolute eosinophilia (n = 1), and azotemia and hyperphosphatemia (n = 10). Serum electrolyte changes included hyponatremia (n = 10), hyperkalemia (n = 9), hypochloremia (n = 9), and hypercalcemia (n = 1). The diagnosis of primary adrenocortical insufficiency was established on the basis of results of adrenocorticotropic hormone (ACTH) stimulation tests (n = 10) and endogenous plasma ACTH determinations (n = 7). Initial therapy for hypoadrenocorticism included intravenous administration of 0.9% saline and dexamethasone and intramuscular administration of desoxycorticosterone acetate in oil. Three cats were euthanatized shortly after diagnosis because of poor clinical response. Results of necropsy examination were unremarkable except for complete destruction of both adrenal cortices. Seven cats were treated chronically with oral prednisone or intramuscular methylprednisolone acetate for glucocorticoid supplementation and with oral fludrocortisone acetate or intramuscular injections of repository desoxycorticosterone pivalate for mineralocorticoid replacement. One cat died after 47 days of therapy from unknown causes; the other six cats are still alive and well after 3 to 70 months of treatment.     

Phenology and spatial and temporal distribution of larval fishes in a partially channelized warmwater stream

We studied the phenology and spatial and temporal dynamics of larval fish abundance with light traps from 5 locations along the length of Luxapalilia Creek, a partially channelized warmwater stream in northeastern Mississippi over 2 spawning seasops (March through August 1992 and 1993). The dominant, early spring spawners were catostomids (early-April to late-May) and darters (mid-March to early-June) whereas summer spawners were mainly cyprinids (mid-May to August) and centrarchids (late-May to August). The relative abundance of larvae collections differed based on: 1) site, 2) location, 3) date, 4) year, and 5) in larval stage. Total numbers of larvae and CPUE were high in mid- to late summer in downstream locations in both years when: 1) temperatures were high, 2) water velocities were low, and 3) depths were shallow compared to upstream locations. More mature larvae (meso- and metalarvae) were more common in the downstream locations whereas less mature larvae (yolk-sac and protolarvae) were more abundant at the upstream locations. The downstream channelized portion of Luxapalila Creek resembled a lentic habitat with littoral zones characterized by slow water velocities, shallow depths, fine sediments, and vegetation. Larvae of darters (Etheostorna and Pcrcina), which require gravel bars and swift currents, were not collected in great numbers downstream, although members of the Ictiobinae (Carpoides and Ictiobus), cyprinidae and centrarchidae (Lepomis spp., Pomoxis spp. and Micropterus spp.) were more abundant downstream than upstream. This suggests that the natural, upstream locations acted as sources of larvae for the channelized downstream location.     

RADIONUCLIDE THYROID IMAGING IN 135 CATS WITH HYPERTHYROIDISM*

Thyroid scanning was performed in 135 hyperthyroid cats and 13 normal cats with technetium-99m as pertechnetate (^99mTcO₄) or with radioactive iodine (¹³¹I). Of the hyperthyroid cats, enlargement and increased radionuclide accumulation were found in one thyroid lobe in 38 (27%) and in both lobes in 97 (73%). In two hyperthyroid cats with thyroid carcinoma, extension of tumor into the thoracic cavity was detected. In normal and hyperthyroid cats the radionuclide images produced with ^99mTcO₄ and ¹³¹I were similar; however, the quality of the ^99mTcO₄ scans was usually better than that of the ¹³¹I scans.     

Excision of the Candystripe1 transposon from a hyper-mutable Y1-cs allele shows that the sorghumY1 gene controls the biosynthesis of both 3-deoxyanthocyanidin phytoalexins and phlobaphene pigments

The 3-deoxyanthocyanidin phytoalexins produced in sorghum leaves in response to Colletotrichum sublineolum have chemical structure similarities to the 3-deoxy flavonoids that are precursors of phlobaphene pigments. Phlobaphenes are commonly observed in the pericarp of mature sorghum grains, while synthesis of 3-deoxyanthocyanidin phytoalexins is a site-specific response to infection with C. sublineolum. We have taken a genetic approach to investigate the possible overlap between the two sub-branches of flavonoid biosynthesis in sorghum that lead to phlobaphenes and 3-deoxyanthocyanidin phytoalexins. A sorghum line with a functional y1 gene synthesizes 3-deoxyanthocyanidins as well as phlobaphenes. However, a progenitor line with the mutable Y1-candystripe (Y1-cs) allele shows variable levels of biosynthesis of these compounds. The Y1-cs allele carries a copy of the Candystripe1 (Cs1) transposable element in the y1 gene. We demonstrate here that the variability in the expression of 3-deoxyanthocyanidins produced in individual mesocotyls of hyper-mutable Y1-cs plants is a function of the activity of the y1 gene. TheCs1 insertion in the Y1-cs allele blocks y1 function, while excision of Cs1 out of they1 locus restores the gene to a functional state. The combined molecular and biochemical characterization of sibling plants confirms that the allelic state of the y1 gene is completely correlated with the production of phytoalexins in response to fungal infection. These results provide support for the idea that the y1 gene regulates the biosynthesis of both 3-deoxyanthocyanidin phytoalexins and phlobaphene pigments in sorghum.