Biomedical subjects
J V Collins
Publications and source records attributed to J V Collins.
The effect of benzoctamine on the ventilatory response to carbon dioxide in normal subjects and in patients with chronic airways obstruction.
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Cryptococcal meningitis as a complication of systemic lupus erythematosus treated with systemic corticosteroids.
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Small airway closure in left heart failure.
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Respiratory depression caused by nitrazepam in patients with respiratory failure.
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Plasma-11-hydroxycorticosteroid levels in drug-induced coma.
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Bronchial asthma with Addison's disease.
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Central venous pressure in acute myocardial infarction.
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Basic equipment for medical intensive-care units.
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A review of experience operating a general medical intensive care unit.
From 18 months' experience of operating a four-bedded general medical intensive care unit a high staff-to-patient ratio was the most important factor in its success. Heavy capital spending does not appreciably reduce the importance of adequate numbers of trained staff, though patient-monitoring equipment can be useful and sometimes vital. As the scope for intensive care widens, the problems of clinical care become difficult, because no doctor is likely to be competent enough to provide for all categories of patients, and there is no intensive care equivalent of the general physician. Intensive care is likely to function best in a divisional specialist system of clinical care.
Gravity-dependent peripheral airway closure in left heart failure.
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Respiratory failure in neuromuscular diseases.
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Prophylaxis of ventricular dysrhythmias following acute myocardial infarction: a double-blind trial of continuous intravenous infusion of lignocaine.
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The effects of salbutamol on pulmonary and systemic haemodynamics.
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Treatment of acute poisoning at Guy's Hospital: October 1969 to September 1970.
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Non-keto-acidotic diabetic coma. The clinical and biochemical features in seven cases and the problems concerned in treatment.
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Intravenous corticosteroids in treatment of acute bronchial asthma.
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Protein uptake into multivesicular bodies and storage granules in the fat body of an insect.
The fat body in Calpodes ethlius (Lepidoptera, Hesperiidae) takes up protein from the blood throughout the larval stage before pupation. Depending upon the phase of development, the protein appears in multivesicular bodies, in large storage granules, and in structures of intermediate form. There are three phases in the 8 days of the last larval stage; the first devoted to growth (molting to 66 hr), the second to synthesis for storage or export (M + 66 to M + 156 hr), and the third to preparation for pupation (M + 156 to pupation at M + 192 hr). From M + O to M + 156 and from M + 180 to M + 188 hr, protein is taken up into multivesicular bodies. Larger MVB's form a continuous series with the protein granules formed from M + 162 to M + 180 hr. Blood proteins increase in concentration and amount from M + 66 to M + 156 hr at the same time as the fat body cells have a high rate of incorporation of amino acids and a structure appropriate for protein synthesis. During granule formation, both amino acid incorporation and blood protein concentration decrease. Since foreign proteins injected into the blood appear in the granules, they are probably made mainly from sequestered blood. Protein uptake involves two stages: concentration between the cells, and ingestion in pinocytotic vesicles. The vesicles fuse to become MVB's or storage granules, depending upon their rates of growth and the addition of lytic enzymes. Since MVB's do not accumulate in the fat body and since many of them contain acid phosphatase and appear empty, they are presumed to be concerned in protein turnover.