Ozone toxicity in the rat. III. Effect of changes in ambient temperature on pulmonary parameters

Wiester, Mildred J., William P. Watkinson, Daniel L. Costa,Kay M. Crissman, Judy H. Richards, Darrell W. Winsett, and Jerry W. Highfill. Ozone toxicity in the rat. III. Effect of changes inambient temperature on pulmonary parameters. J. Appl.Physiol. 81(4): 1691-1700, 1996.Pulmonarytoxicity of ozone (O₃) wasexamined in adult male Fischer 344 rats exposed to 0.5 parts/millionO₃ for either 6 or 23 h/day over 5 days while maintained at an ambient temperature(T_a) of either 10, 22, or34°C. Toxicity was evaluated by using changes in lung volumes andthe concentrations of constituents of bronchoalveolar lavage fluid thatsignal lung injury and/or inflammation. Results indicated thattoxicity increased as T_adecreased. Exposures conducted at 10°C were associated with thegreatest decreases in body weight and total lung capacity and thegreatest increases in lavageable protein, lysozyme, alkaline phosphatase activity, and percent neutrophils.O₃ effects not modified byT_a included increases in residualvolume and lavageable potassium, glucose, urea, and ascorbic acid.There was a progressive decrease in lavageable uric acid with exposureat 34°C. Most effects were attenuated during the 5 exposure daysand/or returned to normal levels after 7 air recovery days,regardless of prior O₃ exposure orT_a. It is possible thatT_a-induced changes in metabolic rate may have altered ventilation and, therefore, theO₃ doses among rats exposed at thethree different T_a levels.

     

Comparative kinetics of fatty acid-amino acid conjugate elicitor biosynthesis by midgut tissue microsomes of Lepidopterous caterpillar larvae

N‐Linolenoyl‐L ‐glutamine is one of several structurally similar fatty acid–amino acid conjugate (FAC) elicitors found in the oral secretions of Lepidopterous caterpillars and its biosynthesis is catalyzed by membrane‐associated alimentary tissue enzyme(s). FAC elicitors comprise 17‐hydroxylated or non‐hydroxylated linolenic acid coupled with L ‐glutamine or L ‐glutamate by an amide bond. We demonstrate in vitro biosynthesis of N‐linolenoyl‐L ‐glutamine by Manduca sexta, Heliothis virescens, and Helicoverpa zea tissue microsomes. Comparison of N‐linolenoyl‐L ‐glutamine biosynthesis kinetics for these species suggests that concurrent biosynthesis and hydrolysis contribute to proportions of FAC elicitors found in their oral secretions. The apparent K_m values for coupling of sodium linolenate were 8.75±0.79, 14.3±3.7 and 20.7±3.4 mM and V_max values were 2.92±0.14, 6.81±1.2 and 4.95±0.55 nmol/min/mg protein for H. zea, H. virescens and M. sexta, respectively. The K_m values for coupling of L ‐glutamine were 10.5±0.26, 22.3±2.0 and 18.9±2.4 mM and V_max values were 1.78±0.21, 3.71±0.50 and 2.49±0.41 nmol/min/mg of protein for H. zea, H. virescens and M. sexta, respectively. © 2010 Wiley Periodicals, Inc.