Stability and factor structure of the Jackson Personality Inventory--Revised.

The Jackson Personality Inventory--Revised comprises 15 bipolar scales and five cluster scores concerning an individual's interpersonal patterns of interaction, cognitive styles, and value orientation. Recent reviews of this revised version raise questions about test-retest stability as well as the factor structure on which cluster scores are based. 74 men and 33 women (29-63 years of age, M = 42.3) completed the inventory while participating in a continuing education program. Of these 45 participated in a second session 13 wk. later. Test-retest correlations are significant, with 12 of the 15 scales having correlations > or = .75. Intercorrelations among all subscales indicate that the Jackson subscales for the most part remain distinct from each other ranging from .01 to .59. A Principal Components Analysis with a varimax rotation yielded three factors that parallel the NEO big five, i.e., Openness, Neuroticism, and Extroversion and replicated previous factor structure found for both versions of the Jackson inventory. The fourth and fifth factors here were labeled Trustworthy and Organization; however, the composition of these factors across several studies appears to be unstable, suggesting optimal certainty when interpreting the clusters of subscales associated only with Openness, Neuroticism, and Extroversion. Further research may help clarify the instability associated with the other factors of this inventory.

Oral contraceptive use: implications for cognitive and emotional functioning.

This study investigated the role of oral contraception use versus nonuse as a moderator variable differentially influencing cognitive-emotional processes. Seventy-six healthy women (29 users and 47 nonusers; 18 to 48 years old), completed the State-Trait Anger Expression Inventory, the Clinical Analysis Questionnaire, the Rotter Scale of locus of control, the Daily Hassles Scale, and a Repertory Grid. A subsample (N = 33) also volunteered for a blood draw. Hormonal levels of progesterone and estrogen mostly were unrelated to cognitive and emotional measures, and contraindicated the "chemical suppression" proposition. Alternatively, when cognitive-emotional functioning was examined separately for users and nonusers, cognitive factors including the appraisal of stress, loci of control, and self-integration were implicated with specific patterns of negative affect and much more so for users than for nonusers. For the most part, oral contraceptive use versus nonuse seemed to influence the saliency rather than the nature of cognitive-emotional patterns. Discussion focused on oral contraceptive use as a moderator variable and the need for longitudinal research to clarify the evolving, biopsychosocial influence of hormonal regulatory treatment.

Sperm count in earthworms (Lumbricus terrestris) as a biomarker for environmental toxicology: effects of cadmium and chlordane.

Earthworms, Lumbricus terrestris, exposed in artificial soil to sublethal concentrations of technical chlordane (6.25, 12.5, and 25 ppm) and cadmium nitrate (100, 200, and 300 ppm) exhibited significant reduction in spermatozoa from testes and seminal vesicles. The onset time of reduction varied with exposure concentration, but absolute depression in sperm count was independent of exposure concentration or exposure duration after reduction was first manifested, demonstrating a threshold effect. Earthworm sperm counts show potential as a rapid-measurement endpoint biomarker for measuring sublethal effects of chemical pollutants on reproduction.

Comparative toxicity of polychlorinated biphenyls to earthworms Eisenia foetida and Lumbricus terrestris.

Effects of polychlorinated biphenyls (PCB; Aroclor 1254) in the manure worm, Eisenia foetida, on survival (LC50/LD50), and ability of coelomic leukocytes (also called coelomocytes) to form secretory rosettes (SR) and erythrocyte rosettes (ER) with, and to phagocytose antigenic rabbit red blood cells were determined and compared with those published for the earthworm, Lumbricus terrestris. Using a 5-day filter paper contact exposure protocol, LC50 and LD50 were 30.4 microg cm(-2) and 4500 microg g(-1) dry mass, respectively. Nominal PCB exposure concentrations of 5.0 and 10.0 microg cm(-2) resulted in tissue levels of 1400 and 2900 microg g(-1) dry mass. These body burdens resulted in significant reduction in SR formation by 18 and 52%, respectively. ER formation and phagocytosis were reduced 52 and 61%, respectively, only at the higher tissue concentration. Compared to L. terrestris, E. foetida: (1) accumulated considerably more PCB at each exposure concentration; (2) showed lower LC50, but higher LD50; and (3) exhibited effects on coelmocytes only at tissue PCB concentrations that caused some mortality. In terms of lethality and immunomodulation of SR, ER and phagocytosis, E. foetida appears to be more resistant to PCB than L. terrestris.

A non-invasive technique for sequential collection of earthworm (Lumbricus terrestris) leukocytes during subchronic immunotoxicity studies.

We have compared two methods for collecting earthworm leukocytes (coelomocytes) with respect to cell yield, viability and behaviour in immunoassays. Non-invasive extrusion was more efficient than puncturing the coelomic cavity. Extrusion does not produce trauma to earthworms maintained under long term laboratory conditions. Neither technique modified immune assays, as determined by erythrocyte and secretory rosette formation, and phagocytosis, since all 3 were functionally equivalent. After an initial extrusion, sequential leukocyte collections by extrusion are possible at intervals of 6 weeks without affecting total and differential cell counts and rosette formation.

Light and electron microscopic demonstration of phospholipase B activity in the mouse eosinophil.

Phospholipase B (EC 3.1.1.5) which hydrolyzes phospholipids in the alpha and beta positions was demonstrated in murine leukocytes using light and electron microscopic histochemical techniques. Leukocytes (neutrophils, lymphocytes, macrophages, eosinophils) were harvested from peritoneal exudates of mice. Cells were fixed in 4% calcium-formol fixative for 10 min at 4 degrees C for light microscopy and 30 min at room temperature for electron microscopy, after which they were incubated at 37 degrees C in medium at pH 6.6 containing 2 microM lysolecithin and CaCl2. The fatty acids released during the hydrolytic reaction were trapped as a calcium precipitate and were converted to a cobalt precipitate for light microscopy by treatment with cobalt acetate or to a lead precipitate for electron microscopy by treatment with lead nitrate. The reaction products were observed to be present in eosinophils and absent in neutrophils, lymphocytes and macrophages. It is concluded that the eosinophilic leukocyte is the carrier cell for phospholipase B in inflammatory reactions.

Effect of anti-thymocyte serum on the eosinophil and lysophospholipase responses in mice infected with Trichinella spiralis.

Anti-thymocyte serum (ATS) was administered to CD-1 mice infected with 100 Trichinella spiralis larvae and its effects on intestinal lysophospholipase (EC 3.1.1.5) activity, peripheral blood lymphocytes and bone marrow, peripheral blood and intestinal eosinophilia were assayed in the same experimental animal. The ATS caused a significant suppression of both the tissue lysophospholipase response and eosinophilia, in all three compartments, when compared to the values found in infected mice that were either treated with normal rabbit serum (NRS) or untreated. The suppressed eosinophil response and reduced lysophospholipase activity demonstrated a close temporal relation throughout the experiment. These findings support the hypothesis that helminth parasite-induced eosinophilia is the cause of increased lysophospholipase activity present in parasitized tissue and that the responses are thymus cell dependent.

Enhanced lysophospholipase activity in sensitized mice challenged with Trichinella spiralis: a role for cell-cooperation.

The relation between lysophospholipase activity and eosinophils was studied using in vivo and in vitro systems. The results support a role for cell cooperation in the eosinophils production of lysophospholipase during a parasitic infection. In vivo experiments demonstrated that the enzyme activity and numbers of tissue eosinophils in immune mice challenged with 200 Trichinella spiralis larvae were not temporally related as previously hypothesized. The data showed that the peak tissue enzyme response occurred well before that of the eosinophil, suggesting increased tissue lysophospholipase activity to be due to more than an increase in numbers of eosinophils infiltrating parasitized tissue. In vitro experiments demonstrated that the eosinophils production of lysophospholipase was influenced by lymphocytes and macrophages after antigen stimulation. We hypothesize that a significant amount of lysophospholipase in parasitized tissue results from each eosinophil synthesizing more of the enzyme after interaction with these cells of the specific immune system.

Enhancement of lysophospholipase activity with Trichinella spiralis antigen: evidence for cell cooperation.

Murine lymphocytes, neutrophils, macrophages and eosinophils were assayed for lysophospholipase in order to determine the cellular source of the enzyme. The eosinophil was the only cell that demonstrated a positive reaction for the enzyme. The role of other cells and/or antigen in production of the enzyme by the eosinophil was also investigated. Results demonstrated that eosinophils cultured with both Trichinella spiralis antigen and other leukocytes (lymphocytes and/or macrophages) yielded enzyme activities significantly greater than did eosinophils cultured alone or with only antigen. More specific experiments showed that T-lymphocytes were the cells responsible for influencing the eosinophils' production of lysophospholipase in the presence of antigen, and that their influence was enhanced by the presence of macrophages. These results suggest that increased lysophospholipase activity present in parasitized tissue is not only due to an increased number of eosinophils infiltrating parasitized tissues, but is also due to each eosinophil synthesizing more of the enzyme for release. The necessity for antigen and other cells suggests a need for cell cooperation in the production of the enzyme, specifically T-lymphocytes and macrophage interaction with the eosinophil.

Intestinal phospholipase B activity in pigs inoculated with transmissible gastroenteritis virus.

Intestinal phospholipase B activity in pigs inoculated with transmissible gastroenteritis (TGE) virus was studied. Phospholipase activity was quantified by measuring the hydrolytic release of free fatty acids in homogenized intestinal tissue incubated with lysophosphatidylcholine. An increase in enzyme activity was observed in the cranial and caudal portions of the ileum and jejunum in pigs killed 3, 6, and 8 days after inoculation with TGE virus. Seemingly, phospholipase B may be part of the host immune response against TGE viral infection.

Effect of anti-eosinophil serum on phospholipase B activity in mice infected with Trichinella spiralis.

Anti-eosinophil serum (AES) was administered to mice infected with 400 Trichinella spiralis larvae and its effect on peripheral eosinophilia and intestinal phospholipase B activity was assayed. The AES caused a significant, temporally related, suppression in both peripheral eosinophilia and phospholipase B activity when compared to responses found in infected mice given normal rabbit serum. The findings support the hypothesis that a parasite-induced eosinophilia is the source of elevated phospholipase B activity present in parasitized tissues.

Intestinal phospholipase B activity in swine inoculated with Trichinella spiralis.

Trichinella spiralis was studied in outbred swine to determine whether infection would cause an increase in intestinal phospholipase B (EC 3.1.1.5) activity and in number of peripheral eosinophils. Intestinal phospholipase B activities increased and were accompanied by eosinophilia. The response was similar to that found in rodents infected with helminth parasites, thus demonstrating that phospholipase B is not unique to rodent models and is probably part of the complex immune response of the host in defense against parasitic infections.