Influence of environment on adrenal cortical response to ACTH stimulation in clinically normal dogs.

Effect of testing environment on adrenal cortical responses to an injection of ACTH in clinically normal dogs was examined in three locations, presumably of increasing order of stress elicitation: in a home; veterinary hospital (VH), 4 hours in a cage; and VH, overnight in a cage. Basal cortisol (hydrocortisone) values for plasma were significantly lower (P less than 0.001) for the home group (1.8 microgram/dl) when compared with values for the VH, 4-hour cage (3.8 microgram/dl) or the VH, overnight cage (3.9 microgram/dl) groups. However, significant differences (P greater than 0.05) were not observed 2 hours after ACTH admininstration for the home group (13.7 microgram/dl); VH, 4-hour cage group (14.8 microgram/dl); or VH, overnight cage group (16.0 microgram/dl). Responses of individual dogs were consistent (P less than 0.005). The testing environment did not markedly affect results of adrenal cortical function tests for dogs when ACTH stimulation was utilized. The response of dogs to ACTH, as monitored by immunologic assay techniques (competitive protein-binding assay or radioimmunoassay), was consistent and was useful as a diagnostic aid for adrenal malfunction.     

Prolactin and colibacillus-induced fluid transport in ligated intestinal segments.

Two experiments, using the ligated intestinal segment technique, were conducted to determine whether the pituitary hormone prolactin (PRL) could reduce Escherichia coli-induced fluid loss into the small intestine of 2- to 3-week-old pigs. Inoculation of 10(6) to 10(8) enteropathogenic E coli organisms into ligated jejunal segments caused a significant accumulation of luminal fluid within 12 hours. In the first experiment, intraluminal inoculation with 0.5 mg of ovine PRL along with the bacteria did not have any effect on fluid accumulation. Systemic IV treatment of the animals with 1.0 mg of ovine PRL at 3-hour intervals, beginning either immediately after or 9 to 10 hours before intestinal ligation, did not significantly (P less than 0.05) reduce fluid accumulation as compared with control animals. In the second experiment, IM administration of 100 microgram of thyrotropin-releasing hormone (TRH) at 3-hour intervals, beginning 6 hours before intestinal ligation, significantly (P less than 0.05) increased circulating PRL concentrations, as measured by radioimmunoassay. However, TRH treatment did not reduce the accumulation of luminal fluid in E coli-inoculated segments.     

Cell-mediated immune responses in cattle adult-vaccinated with Brucella abortus strain 19 and in cattle infected with Brucella abortus field strain.

Cell-mediated immune responses in cattle adult-vaccinated with Brucella abortus strain 19, cattle infected with B abortus field strain, and nonexposed cattle were studied by an in vitro lumphocyte-stimulation test (LST). Lymphocytes were prepared from peripheral bovine blood by the Ficoll-diatrizoate technique, and results were assayed for [3H]thymidine incorporation into DNA by liquid scintillation spectrometry. Serotests and bacteriologic isolation attempts were conducted simultaneously with LST. Lymphocytes from cattle infected with field strains had significantly (P = 0.01) higher specific lymphocyte-stimulation inexposed controls. The LST, the serum standard-tube agglutination test (STT), the Rivanol (RIV) test, and the complement-fixation (CF) test correctly classified cattle from which field strains and strain 19 of B abortus were isolated. The LST was negative in cattle vaccinated with B abortus strain 19 (nonshedding), but the three serotests had many false-positive reactions. The CF test had the least false-positive reaction, followed by the RIV test, and the STT was the least specific. Well before the three serotests became positive, the LST was positive in samples from some cattle during the incubation period of the infection. There was little or no correlation between cell-mediated immune responses (as measured by LST) and serum antibody responses (as measured by STT, RIV test, and CF test) in vaccinated but culture-negative cattle and in some nonvaccinated cattle during the incubation period.     

The influence of temperature on the development of Moniezia expansa (Rudolphi, 1810) in oribatid mites

The life cycle of Moniezia expansa was studied experimentally using 10 species of oribatid mites as intermediate hosts. Four of them became infected, namely Scheloribates laevigatus (76.2%), Sch. latipes (70.8%), Liacarus coracinus (20%) and Platynothrus peltifer (1.1%). The last was found for the first time to serve as intermediate host of M. expansa in Czechoslovakia. The development of the cysticercoid of M. expansa in the oribatid mites at 28 degrees C and 85% relative humidity is completed within 27 days. At 18-20 degrees C and the same relative humidity the development lasts even 97 days.     

Scanning electron microscopic studies on males of trichinella species

Ultrastructure of the cuticle and pseudobursa of adult males of four species of Trichinella has been studied by SEM. T. nativa differs markedly from T. spiralis, T. nelsoni and Trichinella sp. in the form of the pseudobursa. Trichinella sp. differs only slightly from T. spiralis and T. nelsoni. The ultrastructure of the cuticle revealed no characters suitable for the differentiation of the taxons under study.     

Residues of polychlorinated biphenyls and DDT in water and sediment of the St. Lucie Estuary, Florida, 1977.

sigma DDT residues in the St. Lucie River bottom sediments increased after Lake Okeechobee water was discharged through the St. Lucie Canal into the area. sigma DDT levels were highest in sediment samples from the Palm City area, ranging from 1.8 ppb to 6.15 ppb. Sediment samples from the A1A Highway Bridge area contained 1.6-6.8 ppb Aroclor 1254. Levels of polychlorinated biphenyls (PCBs) and sigma DDT in sediment samples from the junction of the St. Lucie and Indian Rivers were not detectable. Surface water samples from the estuary did not show any detectable DDT or PCB residues.