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891.
William I. Jones Jr. Frederick Klein Ralph E. Lincoln Jerry S. Walker Bill G. Mahlandt James P. Dobbs 《Journal of bacteriology》1967,94(3):609-614
Quantitative measurements of mean time to death, percentage of survivors, and viable cell populations in the whole body were employed to determine the effects of penicillin, dihydrostreptomycin, chlortetracycline, oxytetracycline, chloramphenicol, and antiserum on the course of anthrax infection in mice. By all parameters tested, penicillin and dihydrostreptomycin were most effective in the treatment of the disease. Therapy initiated in the later stages of the disease was more effective than that initiated in the earlier stages. Quantitative studies indicated that it was more difficult to eliminate organisms from the kidney than from any other organ or tissue. These measurements for the evaluation of antibiotic therapy are suggested for the study of other bacterial diseases. 相似文献
892.
893.
894.
Alfred Frederick Bliss 《The Journal of general physiology》1946,29(5):277-297
1. While several reports of photosensitive pigments from the retinas of animals possessing large numbers of cone cells have been published, the only study which could be confirmed was Wald''s discovery of iodopsin, a red-sensitive pigment from chicken eyes. 2. In its chemical properties, such as the range of pH stability and the effect of polar organic solvents, iodopsin resembles rhodopsin but is considerably more labile. 3. A partial purification from inert yellow impurities has been effected by prehardening the retinas in pH 4.9 acetate buffer before extraction by 2 per cent digitonin. Rhodopsin was an inevitable contaminant in most methods of extraction, but could be reduced to about 10 per cent of the absorption due to iodopsin by extraction of unhardened retinas with 4 per cent Merck''s saponin in ¾ saturated magnesium sulfate for about 1 hour. 4. The rate of bleaching of iodopsin was found to be first order and linear with respect to energy. 5. The bleaching effectiveness spectrum of iodopsin was determined with the aid of color filters of known energy transmission, and shows a maximum at 560 mµ in the yellow green with a lower plateau in the blue. The spectrum is in good agreement with the sensitivity of the human cones except for the wavelength of maximum bleaching effectiveness. The maximum sensitivity of the human cones is found at 540 mµ. 6. Previous reports of changes in pH and inorganic phosphate level of retinas due to bleaching could not be confirmed. 相似文献
895.
896.
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898.
Lancelot Barrington-Ward Hubert Bond Edwin Bramwell Duncan C. L. Fitzwilliams Francis Fraser R. S. Frew William Goschen F. J. McCann Macmillan Arthur MacNalty Frederick Kay Menzies George Newman George Riddoch Humphry Rolleston Bertram Shires Frederick Still G. A. Sutherland James Taylor James Walton David Wilkie 《BMJ (Clinical research ed.)》1938,2(4046):195-196
899.
Nerve Growth Factor Potentiates Bradykinin-Induced Calcium Influx and Release in PC12 Cells 总被引:2,自引:0,他引:2
Andrew B. Bush Laurence A. Borden Lloyd A. Greene Frederick R. Maxfield 《Journal of neurochemistry》1991,57(2):562-574
To investigate how the response to agonists changes during neuronal differentiation, we examined the effect of nerve growth factor (NGF) on bradykinin-induced calcium increases in PC12 cells. Short-term (1 h) treatment with NGF increased the potency of bradykinin to raise intracellular calcium by about 10-fold, whereas long-term (1 week) treatment, which was associated with the expression of the differentiated phenotype, increased the potency about 100-fold. Neither treatment affected the maximal response to bradykinin. NGF alone had no acute effect on calcium levels. Short-term potentiation appeared to be mainly a result of greater release of calcium from intracellular stores, whereas the effect of long-term treatment apparently was due to increases in both release from intracellular stores and calcium influx. [3H]Bradykinin binding to intact PC12 cells was unaltered by short-term NGF treatment, whereas differentiated cells displayed a 50% increase in receptor number and about a twofold increase in affinity as compared with cells not treated with NGF. The production of inositol phosphates in response to bradykinin correlated poorly with the calcium transients, in that large calcium responses were associated with small increases in inositol phosphates. Neither NGF treatment had a significant effect on the appearance of inositol phosphates in response to bradykinin. Experiments with permeabilized cells revealed that differentiated cells did not display a heightened response to exogenously added inositol 1,4,5-trisphosphate. Our results demonstrate that NGF modulates the bradykinin signaling pathway without acutely activating this pathway itself. 相似文献
900.
Frederick L. Crane Iris L. Sun Rita Barr Hans Löw 《Journal of bioenergetics and biomembranes》1991,23(5):773-803
Transplasma membrane electron transport in both plant and animal cells activates proton release. The nature and components of the electron transport system and the mechanism by which proton release is activated remains to be discovered. Reduced pyridine nucleotides are substrates for the plasma membrane dehydrogenases. Both plant and animal membranes have unusual cyanide-insensitive oxidases so oxygen can be the natural electron acceptor. Natural ferric chelates or ferric transferrin can also act as electron acceptors. Artificial, impermeable oxidants such as ferricyanide are used to probe the activity. Since plasma membranes containb cytochromes, flavin, iron, and quinones, components for electron transport are present but their participation, except for quinone, has not been demonstrated. Stimulation of electron transport with impermeable oxidants and hormones activates proton release from cells. In plants the electron transport and proton release is stimulated by red or blue light. Inhibitors of electron transport, such as certain antitumor drugs, inhibit proton release. With animal cells the high ratio of protons released to electrons transferred, stimulation of proton release by sodium ions, and inhibition by amilorides indicates that electron transport activates the Na+/H+ antiport. In plants part of the proton release can be achieved by activation of the H+ ATPase. A contribution to proton transfer by protonated electron carriers in the membrane has not been eliminated. In some cells transmembrane electron transport has been shown to cause cytoplasmic pH changes or to stimulate protein kinases which may be the basis for activation of proton channels in the membrane. The redox-induced proton release causes internal and external pH changes which can be related to stimulation of animal and plant cell growth by external, impermeable oxidants or by oxygen. 相似文献