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S M Kennedy

Publications and source records attributed to S M Kennedy.

At least 91 records · Page 5Linked to original sources

Selecting experimental data for use in quantitative risk assessment: an expert-judgement approach.

In many cancer risk assessments the experimental data used in statistical modeling are selected by applying generic guidelines. The guidelines exclude use of some types of experimental data and often appear arbitrary since rules rather than scientific judgments guide selection of data. This paper implements an alternative approach in which data are selected based on the judgments of practicing scientists. Eight such scientists were identified through an explicit selection procedure to help select data for use in a dose-response assessment of formaldehyde. Judgements about appropriate data sets were then elicited in personal interviews using a formal interview protocol. Appropriate data sets were fit to the multistage model and used as the basis for low-dose extrapolation. Low-dose risk estimates are shown to be sensitive to the selection of data, especially the treatment of benign tumors. The recommendations of the experts also differ in some respects from the choices made in previously published risk assessments. This suggests that scientific judgement may be an appropriate method to augment guidelines when a broad range of data is available. The paper argues that the expert judgment approach has some advantages that are worth considering.

Air Pollutants↗

Acute pulmonary responses among automobile workers exposed to aerosols of machining fluids.

Previous investigations of workers exposed to machining fluids have shown increased rates of cough and phlegm and have shown that these exposures may cause occupational asthma. To examine acute responses to these agents, cross-shift lung function changes related to machining fluid aerosols among 89 machine operators at two factories producing automobile parts were measured and compared with the findings for 42 unexposed assembly workers studied similarly at the same factories. Workers wore a personal air-sampling device on a Monday and Friday of a working week, and spirometry was performed before and after the work shifts on both days. On Mondays, a 5% or greater decrease in the forced expiratory volume in 1-second (FEV1), regarded as an "FEV1-response," occurred in 23.6% of the machinists and in only 9.5% of the assembly workers (relative risk = 2.5, p less than .05). After adjusting statistically for a history of childhood asthma, for smoking prior to lung function testing, and for race, odds ratios for an FEV1-response of 4.4 among workers exposed to aerosols of straight mineral oils, 5.8 for oil emulsions, and 6.9 for synthetic fluids were found. The FEV1-responses on Fridays were similar to those on Mondays. There was no progressive decline in FEV1 over the work week. Personal air samples, collected with a two-stage impactor, allowed aerosol masses to be measured in three size fractions: less than 3.5 microns, 3.5-9.8 microns, and greater than 9.8 microns aerodynamic diameter. Exposure levels to each type of machining fluid were remarkably similar within each size fraction and for total aerosol levels. Total aerosol concentrations for assembly workers ranged from 0.07 to 0.44 mg/M3, and for machinists from 0.16 to 2.03 mg/m3. Inhalable particle (less than or equal to 9.8 microns) levels were derived from the sum of the air concentrations in the two smallest-size fractions, and significant cross-shift decrements in FEV1 on Mondays and Fridays were associated with inhalable aerosol levels greater than 0.20 mg/m3. These findings show that acute airflow obstruction is associated with exposures to aerosols of various machining fluids and that airway responses occur well below current recommended exposure limits.

Aerosols↗

Stimulation by parathyroid hormone of calcium absorption in confluent Madin-Darby canine kidney cells.

Parathyroid hormone (PTH) increases renal calcium absorption exclusively in cortical thick limbs and distal tubules. Lack of sufficient tissue has precluded detailed biochemical study of the mechanisms responsible for the hypercalcemic effect of PTH. Therefore, we assessed PTH action on calcium transport in Madin-Darby canine kidney (MDCK) cells, a cell line expressing distal characteristics, to determine its suitability as a model for analyzing PTH action. Calcium transport across MDCK cells grown to confluence on porous filters was measured at 37 degrees C in Ussing chambers. Mucosal-to-serosal calcium fluxes (JCa, mol/min cm-2 x 10(-9)) were measured with 45Ca at -3, -1, 5, 10, and 20 min; agonist was added at 0 min. Basal JCa averaged 0.98. PTH at 0.2 microM increased JCa by 12% (P less than 0.05) and 1 microM PTH by 70% (P less than 0.01). Calcitonin (1 microM) had no effect on JCa. The fact that high concentrations of dibutyryl cAMP (1 mM) and forskolin (10 microM) increased JCa by only 37% and 22%, respectively, suggested that cAMP-independent mechanisms may participate in PTH-stimulated JCa. Therefore we examined the effect of other putative second messengers. In the presence of 2 mM external [Ca], 10 nM A23187 increased JCa by 88%, and 10 microM A23187 increased JCa by 121%. Addition of 10 microM phorbol 12-myristate 13-acetate (PMA) increased JCa by 60%. We conclude that: 1) PTH specifically stimulates unidirectional calcium absorption in MDCK cells; 2) both adenylate cyclase-coupled and calcium-coupled receptors may participate in signaling the response to PTH; and 3) confluent MDCK cells represent a useful experimental model for elucidating the biochemical mechanisms involved in the renal hypercalcemic action of PTH.

Absorption↗

Cotton dust and endotoxin exposure-response relationships in cotton textile workers.

Endotoxin exposure has been implicated in the etiology of lung disease in cotton workers. We investigated this potential relationship in 443 cotton workers from 2 factories in Shanghai and 439 control subjects from a nearby silk mill. A respiratory questionnaire was administered and pre- and postshift forced expiratory volume (FVC) and flow in one second (FEV1) were determined for each worker. Multiple area air samples were analyzed for total elutriated dust concentration (range: 0.15 to 2.5 mg/m3) and endotoxin (range: 0.002 to 0.55 microgram U.S. Reference Endotoxin/m3). The cotton worker population was stratified by current and cumulative dust or endotoxin exposure. Groups were compared for FEV1, FVC, FEV1/FVC%, % change in FEV1 over the shift (delta FEV1%), and prevalences of chronic bronchitis and byssinosis, and linear and logistic regression models were constructed. No dose-response relationships were demonstrated comparing dust concentration to any pulmonary function or symptom variable. A dose-response trend was seen with the current endotoxin level and FEV1, delta FEV1%, and the prevalence of byssinosis and chronic bronchitis, except for the highest exposure level group in which a reversal of the trend was seen. The regression coefficients for current endotoxin exposure were significant (p less than 0.05) in the models for FEV1 and chronic bronchitis but not in the models for delta FEV1% (i.e., acute change in FEV1) or byssinosis prevalence. The coefficient for dust level was never significant in the models.(ABSTRACT TRUNCATED AT 250 WORDS)

Air Pollutants, Occupational↗

Diversion colitis. Pathologic findings in a resected sigmoid colon and rectum.

We present here the detailed pathologic findings in the resected colon and rectum from a paraplegic patient with severely symptomatic diversion colitis and lack of anorectal function. Previous reports of the pathology of this condition have been confined to biopsy findings. A diffuse nodularity caused by lymphoid hyperplasia and an inflammatory process confined to the colorectal mucosa with erosions, crypt abscesses, mucin granulomas, and aphthoid ulcers were the main features. There was minimal distortion of crypt architecture. The pathologic features of this entity are compared to those of other inflammatory disorders of the colon and rectum.

Adult↗

Induction of UDP-glucuronyl transferase mRNA in embryonic chick livers by phenobarbital.

Administration of phenobarbital to chick embryos increased hepatic microsomal UDP-glucuroyltransferase activity some 25-fold. The large phenobarbital-induced increase of UDP-glucuronyltransferase activity was correlated to an equivalent increase of immunochemically measurable UDP-glucuronyltransferase protein. Poly(A+) RNA isolated from the livers of chick embryos treated with either phenobarbital or saline was translated in vitro. Immunochemical analysis of the translation products indicated that phenobarbital induced a 30-fold increase in UDP-GT mRNA. Fractionation of hepatic poly(A+) RNA from phenobarbital-treated chick embryos by sucrose density gradient centrifugation indicated that the size of the UDP-GT mRNA was 21S. These data show that phenobarbital induction of chick embryo liver UDP-glucuronyltransferase activity correlates with a similar large increase in the level of translatable mRNA for this enzyme.

Animals↗

Pulmonary function and peripheral airway disease in patients with mineral dust or fume exposure.

Cigarette smoking and mineral dust exposure combined result in small airways function abnormalities difficult to distinguish from smoking effects alone. To determine if mineral dust or fume exposure in smokers results in additional changes in small airways structure and function, we studied small airways disease and pulmonary function in 25 persons (62.4 +/- 8.8 yr) with exposure to mineral dust or fume for 10 yr or more and compared them individually with control subjects without dust exposure (61.8 +/- 8.5 yr) matched for age, smoking history, and lobe resected. All subjects were patients undergoing surgical resection for isolated coin lesions. Occupational histories and measurements of lung volumes, flow rates, small airways function, diffusing capacity, and pressure-volume relationships were obtained preoperatively. Membranous bronchioles were graded for the presence and degree of mural inflammation, fibrosis, muscle, pigment, and squamous and goblet cell metaplasia. Respiratory bronchioles were similarly graded for inflammation, fibrosis, muscle, pigment, and lumenal macrophages. The dust-exposed group had increased fibrous tissue deposition and goblet cell metaplasia in the membranous bronchioles (p less than 0.05). When the exposed group was divided according to occupation into miners (n = 13) and nonminers exposed in other dusty jobs (n = 12), the pathologic changes were evident in both exposed groups. No differences in pulmonary function were seen between the 2 groups. We conclude that occupational exposure to mineral dust and fume produces structural changes in peripheral airways that are greater than those seen with smoking alone, but these changes were not associated with a greater deterioration in lung function.

Aged↗

Macrophage accumulation of inhaled gallium-67 citrate in normal lungs.

Injected 67Ga has been used extensively to monitor inflammatory processes in the peripheral lung. We hypothesized that inhaled 67Ga may be useful in marking early airway inflammation in smokers. Eight nonsmokers and eight smokers breathed a 67Ga aerosol and imaging was performed immediately and 24 and 96 hr later. Approximately two-thirds of the initial dose remained in the lungs at 24 hr in both groups and no difference was seen between the groups. Only a very slight decrease was seen in both groups at 96 hr suggesting the gallium becomes bound to lung tissue or to cells not rapidly removed from the lungs. Autoradiography was performed on tissue from two smoke-exposed guinea pigs and two human patients undergoing resection surgery who breathed the gallium aerosol 24 hr prior to tissue removal. Silver grain accumulations were seen only over macrophages. We conclude that macrophage associated accumulation of 67Ga occurs in healthy lungs, and that it is not feasible to use aerosolized gallium to assess airway inflammation in smokers.

Adult↗

Increased airway mucosal permeability of smokers. Relationship to airway reactivity.

We studied pulmonary epithelial permeability and bronchial reactivity in 10 smoking and 8 nonsmoking adults. Permeability was measured as the disappearance half-life (T 1/2) of aerosolized 99mTc-DTPA from the lungs, and a permeability index (PI) calculated that reflected the appearance of the tracer in the blood. Smokers had increased permeability with a T 1/2 of 44.6 +/- 12.2 min and PI values at 10, 25, and 60 min of 27.3 +/- 13.2, 32.5 +/- 10.2, and 34.3 +/- 9.9, compared with those in nonsmokers with a T 1/2 of 110.0 +/- 62.7 min and PI values of 9.4 +/- 5.7, 14.9 +/- 8.3, and 23.1 +/- 9.0. Bronchial reactivity to histamine was measured with and without prior exposure to aerosolized propranolol (to achieve beta-blockade of airway smooth muscle). Reactivity increased significantly (p less than 0.001) in both groups after beta-blockade, but no difference was found between smokers and nonsmokers. Despite the increased permeability in smokers, there was no evidence of increased reactivity.

Adrenergic beta-Antagonists↗

Single-step purification of epoxide hydrolase from rat liver microsomes using monoclonal-antibody chromatography.

Monoclonal antibody to rat liver microsomal epoxide hydrolase has been obtained after immunization of mice with the enzyme prepared by conventional methods. Antibody from ascitic fluid was purified and coupled to CNBr-activated Sepharose 4B, to give a specific affinity column. Monoclonal-antibody affinity chromatography provided a rapid single-step method of purifying to homogeneity active epoxide hydrolase from crude solubilized microsomes. The techniques used offer an effective method for characterization of a non-inhibitory monoclonal antibody.

Animals↗

Immunochemical comparison of UDP-glucuronyltransferase from Gunn- and Wistar-rat livers.

1. Antiserum was raised against purified Wistar-rat liver UDP-glucuronyltransferase. 2. UDP-glucuronyltransferase activities towards 4-nitrophenol, bilirubin, 1-naphthol and morphine were co-immunoprecipitated from solubilized Wistar-rat liver preparations. 3. UDP-glucuronyltransferase activities towards 1-naphthol, 2-aminophenol and 4-nitrophenol were precipitated from solubilized Gunn-rat liver preparations by this antiserum. 4. UDP-glucuronyltransferase activities towards 1-naphthol, 4-nitrophenol and bilirubin, from Wistar-rat liver, were slightly inhibited by antiserum, whereas 1-naphthol UDP-glucuronyltransferase activity from Gunn-rat livers was greatly inhibited. 5. Measurable Wistar-rat liver glucuronyltransferase activities in washed immunoprecipitates indicate that the enzyme(s) were not merely inhibited by antiserum. 6. Immunoglobulin G purified from this antiserum immunoprecipitated transferase activities towards 4-nitrophenol, bilirubin and 1-naphthol. 7. The washed immunoprecipitates from both rat strains, containing UDP-glucuronyltransferase activity, appear to be similar when analysed by sodium dodecyl sulphate/polyacrylamide-gel electrophoresis. 8. Radial-immunodiffusion studies suggest that a smaller amount of UDP-glucuronyltransferase protein is present in Gunn-rat liver than in Wistar-rat liver. 9. The significance of these results in relation to the genetic deficiency in the Gunn rat is discussed.

Animals↗

Cyclobutane analogs of GABA.

Both cis- and trans-3-aminocyclobutane-1-carboxylic acid have been synthesized as conformationally restricted analogs of GABA. The cis isomer displayed weak to moderate GABA-like activity with respect to (1) inhibition of GABA uptake in rat brain minislices, (2) inhibition of sodium-independent binding of GABA to rat brain membranes, (3) activity as a substrate for GABA aminotransferase. and (4) depression of the firing rate of cat spinal neurons in vivo. The trans isomer was less effective on all four assays. The results has been interpreted in terms of the conformational "pinning back" of the polar groups by the cyclobutane ring in the trans GABA analog so that unfavorable steric interactions would occur between one of the methylene groups and a region of steric hindrance at the active sites for particular GABA processes.

4-Aminobutyrate Transaminase↗