Biomedical subjects
Publications and source records attributed to R P Herman.
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The resource island hypothesis predicts that soil resources such as nitrogen, phosphorus, and water will be distributed evenly in grasslands but have a patchy distribution focused around plants in shrublands. This hypothesis predicts that microorganism numbers will follow resources and be (i) evenly distributed in grasslands, (ii) concentrated around individual plants in shrublands, and (iii) higher where resources are higher when comparing the same vegetation type. This study enumerated total heterotrophic bacteria and a subset of these, the nitrogen-efficient guild (NEG), in three shrublands (playa fringe mesquite, tar bush, and creosote) and two grasslands (playa and bajada). Both heterotrophs and NEG members followed the distribution pattern predicted by the resource island hypothesis. There were no significant differences in heterotroph or NEG numbers comparing at-plant and interplant samples for both the playa and bajada grasslands. Furthermore, populations were generally higher in nutrient-rich playa grasslands than nutrient-poor bajada grasslands. In contrast, both heterotroph and NEG numbers were higher at shrubs than between shrubs in all three shrub sites. These results suggest that resource abundance in resource islands predicts the distribution of heterotrophic bacterial numbers in desert soils.
This study examined the temporal and spatial variation in the populations of bacteria from a Chihuahuan desert bajada grassland that could grow on nearly nitrogen-free medium, a nitrogen-efficient guild (NEG). A Curtis similarity index of 0.876 and nearly identical diversity and equability indexes (H' = 1.22, J = 0.46 and H' = 1.27, J = 0.48 for the crown edge and interplant samples, respectively) indicated that there was no qualitative difference between the NEG assemblages isolated from samples taken at Bouteloua eriopoda plant crowns and in nonvegetated areas 45 cm from crowns. The difference in NEG populations between the crown and interplant samples was only 2-fold, despite a 9.5-fold difference in root biomass between the sites. These differences, while consistent, were statistically significant at only 50% of the sampling times. There was over an order of magnitude difference in NEG numbers in root-associated soil and in bulk soil from the crown or intercrown sites. The typical trend for temporal variation in NEG numbers was that they increased in the spring, fluctuated dramatically over the summer, and declined at the summer's end. The pattern of soil moisture change was the only abiotic variable which showed the same fluctuation pattern as NEG numbers.
In this study we measured changes in population levels of free-living N2-fixing bacteria in the root zones of potted Bouteloua eriopoda and Sporobolus flexuosus plants as well as the photosynthetic indices of the plants in response to added nitrogen, added water, and added water plus nitrogen treatments. In addition, N2 fixer population changes in response to added carbon source and nitrogen were measured in plant-free soil columns. There were significant increases in the numbers of N2 fixers associated with both plant species in the water and the water plus nitrogen treatments. Both treatments increased the photosynthetic index, suggesting that plant exudates were driving N2 fixer population changes. Population increases were greatest in the water plus nitrogen treatments, indicating that added nitrogen was synergistic with added water and suggesting that nitrogen addition spared bacteria the metabolic cost of N2 fixation, allowing greater reproduction. Plant-free column studies demonstrated a synergistic carbon-nitrogen effect when carbon levels were limiting (low malate addition) but not when carbon was abundant (high malate), further supporting this hypothesis. The results of this study indicate the presence of N2 fixer populations which interact with plants and which may play a role in the nitrogen balance of desert grasslands.
Leukotrienes (LTs) have been shown to cause contraction of mammalian airway smooth muscle. In this study, LTC4, LTD4, and LTE4 were tested on isolated strips of bullfrog lung. LTC4, LTD4, and LTE4 (10(-7) to 3 x 10(-10) M) stimulated lung contraction. LTC4 was the most potent, with LTD4 and LTE4 being of equal but lower potency. The cyclooxygenase inhibitors, indomethacin and ibuprofen, had no effect on the strength of leukotriene-induced contraction. In addition, the effects of three mammalian LTD4 receptor antagonists, L-649,923, L-648,051, and LY171883 were tested. All three antagonists failed to block LTC4-simulated contraction, but were effective blockers of LTD4. LTE4-stimulated contractions were significantly blunted by all three antagonists, but the extent of blockade was less than for LTD4. Significant bioconversion of [3H]LTC4 to LTD4 and LTE4 occurred in minced lung preparations but not in lung strips. Peptide leukotrienes caused contraction in amphibian lung, though the order of potency differs from mammals. Like mammals, frogs appear to have two classes of leukotriene receptors, one for LTC4 and one for LTD4-LTE4. These results support the hypothesis that leukotriene receptors have been highly conserved through evolution, despite the fact that the nature of tissue responsiveness to leukotrienes has changed over evolutionary time.
The effects of leukotrienes (LTs) have been widely studied in the isolated perfused mammalian heart; however, little is known about the effect or metabolism of LTs in the isolated bullfrog heart. Isolated perfused bullfrog hearts were administered randomized doses of LTC4, LTD4, or LTE4. The cardiac parameters of heart rate, developed tension, and its first derivative (dT/dt) were recorded. LTC4 was the most potent of the leukotrienes tested in eliciting positive inotropic effects. LTD4 and LTE4 were equally effective but about one order of magnitude less potent than LTC4. None of the LTs showed any chronotropic effects in this preparation. A series of [3H]LTC4 metabolism experiments were carried out using whole perfused hearts and minced bullfrog heart tissue. Isolated perfused bullfrog hearts administered [3H]LTC4 converted significant amounts to [3H]LTD4, and to a lesser degree, [3H]LTE4, during the 6-min course of collection. Both minced atrial and ventricular tissue converted [3H]LTC4 to radioactive metabolites that co-migrated with authentic LTD4 and LTE4 standards. In both tissues, the major product was [3H]LTD4, with smaller amounts of [3H]LTE4 produced. The atrium converted significantly more [3H]LTC4 to its metabolites than did the ventricle. The metabolism of [3H]LTC4 to [3H]LTD4 by both tissues was virtually abolished in the presence of serine borate. Cysteine had no effect on [3H]LTE4 production. The data in this study demonstrate that leukotrienes have the opposite inotropic effect on the heart when compared with mammals. Also in contrast to mammals, frogs metabolize LTC4 to a less potent compound and may use the LTC4 to LTD4 conversion as a mechanism of LTC4 inactivation.
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Isolated perfused bullfrog hearts were administered randomized doses of LTC4, LTD4 or LTE4. The cardiac parameters of heart rate, developed tension and its first derivative (dT/dt) were recorded. LTC4 was the most potent of the leukotrienes tested in eliciting positive inotropic effects. LTD4 and LTE4 were equally effective but about one order of magnitude less potent than LTC4. None of the LTs showed any chronotropic effects in this preparation. LTC4 was significantly more potent in the presence of L-serine borate, an inhibitor of gamma-glutamyl transpeptidase, than in its absence, raising the possibility of significant bioconversion of LTC4 by the bullfrog heart. 3H-LTC4 metabolism experiments were carried out using whole perfused hearts or minced bullfrog heart tissue. During the six minute course of collection, the isolated perfused heart converted significant amounts of LTC4 to LTD4 and to a lesser degree LTE4. This conversion was attenuated in the presence of L-serine borate. Both minced atrial and ventricular tissue converted 3H-LTC4 to radioactive metabolites which co-migrated with authentic LTD4 and LTE4 standards. In both tissues, the major product was LTD4, with smaller amounts of LTE4 produced. The atrium converted significantly more LTC4 to its metabolites than did the ventricle. The metabolism of LTC4 to LTD4 by both tissues was virtually abolished in the presence of serine borate. It is interesting that LTC4 metabolism pattern and rate is comparable in mammals and frogs in spite of the fact that the inotropic effects of leukotrienes are opposite in the two taxa and, in frogs, metabolism results in a less potent agent.
While the cardiovascular effects of the sulfidopeptide leukotrienes (LTs) have been well studied in mammals, their effects are not well known in lower vertebrates. American bullfrogs (Rana catesbeiana) were cannulated in the right sciatic artery and left sciatic vein. In some studies an additional ventricular cannula was implanted. LTC4, LTD4, and LTE4 were compared for their cardiovascular actions by infusion via the sciatic vein into the unanesthetized animals. While all three leukotrienes decreased mean arterial pressure (MAP) and increased heart rate (HR), LTC4 was found to be more potent than the other leukotrienes. In bullfrogs with ventricular cannulae to measure ventricular pressure (VP) and its derivative (+ dP/dt), LTC4 had negative inotropic effects which were blunted by indomethacin (4 mg/kg-bw). 3H-LTC4 metabolism studies were carried out using blood and plasma to examine conversion to other products. Following incubation for 12 min and extraction by C18 Sep-Pak cartridges, samples were analyzed by high performance liquid chromatography. In whole blood, but not in plasma, 3H-LTC4 was rapidly converted to a compound with the retention time of the LTD4 standard. Little conversion to LTE4 was observed within the time course of the experiment. The data suggest that cardiovascular effects of LTC4 may be greater than those observed, since LTC4 is rapidly metabolized to a less active compound. The effects of LTC4 may, in part, be due to stimulation of synthesis of cyclooxygenase metabolites. The ability to record the effects of leukotrienes uncomplicated by effects on coronary arteries make the bullfrog an excellent model for comparative studies on the cardiovascular effects of leukotrienes.
The metabolites of inflammatory cells produced by massive infection of the peritoneal cavity of two related European species of frogs, Rana temporaria and Rana arvalis were examined for lipoxygenase-generated products of exogenous arachidonic acid. Cells of Rana temporaria produced large amounts of 5-hydroxyeicosatetraenoic acid and leukotriene B4. Cells from Rana arvalis produced only 15-hydroxyeicosatetraenoic acid. This is the first unequivocal demonstration of such enzyme activity in lower vertebrates. There was a trend towards increased mortality in the species without evidence of 5-lipoxygenase activity.
Ten frogs (Xenopus laevis) were injected with mixed bacteria to produce a septic peritonitis. Peritoneal inflammatory cells of eight animals were studied for monohydroxyeicosanoid and leukotriene production from exogenous arachidonic acid. Large amounts of 12-hydroxyeicosatetraenoic acid were produced; smaller amounts of 5- and 15-hydroxyeicosatetraenoic and leukotriene B4 were produced. Identifications were confirmed by retention times on HPLC, ultraviolet spectroscopy on all products, and gas chromatograph/mass spectrometry in the case of 12-hydroxyeicosatetraenoic acid.
The soluble hydroperoxide isomerase and 15-lipoxygenase activities were partially purified from the oomycete Saprolegnia parasitica and some of their properties characterized. Both enzymes co-eluted with a molecular weight of 145,000-150,000 on Sephacryl S-300 chromatography. The enzyme activities also co-eluted on DEAE Sephadex ion exchange chromatography and hydroxylapatite chromatography. Both activities showed similar responses to pH and temperature. Both enzymes showed parallel inhibition by p-hydroxymercuribenzoate and eicosatetraynoic acid. The partially purified hydroperoxide isomerase showed an apparent km of 166 microM and a Vmax of 5.3 mumol/min/mg protein for exogenous 15-HPETE. It was not stimulated by calcium. These results suggest that the soluble hydroperoxide isomerase and 15-lipoxygenase activities from S. parasitica are both contained on the same protein or protein complex.
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[1-14C]Arachidonic acid was incubated with homogenates of the fungus, Saprolegnia parasitica. The products consisted of comparable amounts of two epoxy alcohols, 15-Ls-hydroxy-11,12-epoxy-5cis,8cis,13trans- eicosatrienoic acid and 15-hydroxy-13,14-epoxy-5cis,8cis,11cis-eicosatrienoic acid. Results of incubations carried out in the presence of nordihydroguaiaretic acid, 5,8,11,14-eicosatetraynoic acid, p-hydroxymercuribenzoate as well as glutathione peroxidase plus reduced glutathione demonstrated that transformation of arachidonic acid into epoxy alcohols occurred with the formation of 15-Ls-hydroperoxy-5cis,8cis,11cis,13trans- eicosatetraenoic acid (15-HPETE) as an intermediate. The pathway involved a lipoxygenase catalyzing the oxygenation of arachidonic acid at the 15L position to produce 15-HPETE, and a hydroperoxide isomerase activity which catalyzed conversion of 15-HPETE into the two epoxy alcohols. Studies with 15-[18O2]HPETE demonstrated that both oxygens of 15-HPETE were retained in the epoxy alcohols. Furthermore, experiments with mixtures of 15-[18O2]-and 15-[16O2]HPETE showed that conversion of 15-HPETE into epoxy alcohols occurred by an intramolecular transfer of hydroperoxide oxygen.
The prostaglandin synthesis inhibitors aspirin and indomethacin inhibit the growth of Achlya caroliniana, A. ambisexualis and Saprolegnia parasitica in a dose-related manner. In addition, the inhibitors cause the formation of a characteristic asterisk-shaped colony. This abnormal colony morphology does not appear to be dependent on medium composition, since three different nitrogen and five differentcarbon sources all support the abnormal growth in the presence of 0.1 mM indomethacin. The abnormal colony morphology is the result of abnormal branching. Inhibitor grown colonies are more densely branched than controls, with shorter distances between branches. Inhibited colonies allowed to grow for greater than ten days escape the inhibition and assume a normal gross colony morphology and size, however, they do not reproduce sexually. The addition of 2 micrograms/ml PGF1 alpha to the growth medium partially overcomes the growth inhibition caused by indomethacin. The data suggest a role for prostaglandin or prostaglandin-like compounds in oomycete development.
The antitubercular drug isoniazid (INH) was hown by radio-chromatographic studies to react with tyrosine in growth medium. Exogenous tyrosine added to the growth medium interfered with the inhibitory action of INH on Mycobacterium phlei. These observations were confirmed by difference spectra studies which showed that tyrosine would react with INH as long as the tyrosine phenolic hydroxyl group was not blocked. These results led to the hypothesis that INH could exert its influence by interfering with tyrosine residues in mycobacterial proteins. N-acetylimidazole, a tyrosine-acetylating agent, mimicked the action of INH on the reduced nicotinamide adenine dinucleotide oxidase and dehydrogenase activity in electron transport particles from wild-type and INH-resistant M. phlei. Pyrazinamide, a drug structurally related to INH, also mimicked its effect on electron transport particles. To confirm that INH could react with tyrosine in proteins, purified enzymes with known tyrosine positions were tested. Bovine carboxypeptidase A with tyrosine at the active site was inhibited by INH and N-acetylimidazole, whereas the controls, yeast alcohol dehydrogenase and ribonuclease A, were not. It is therefore proposed that tyrosine residues in proteins may serve as the target for INH action in mycobacteria.