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FILE NAME: Chemical Abstracts (CHAB) DATE: 1931 DOC#: CHAB005 DOCUMENT DESCRIPTION: Abstract Originally Published in 1931 by Simson
1931
11--Biological Chemistry, H --Pharmacology
2201
J oseph B. Wolffs and Samubl Bettbt. Ann. Internal Med. 4, 795-803(1931).
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J ohn T. M yers
Tnbromoethanol anesthesia. , R alph W. Waters and G. W. M ubhlbbrger.
Arch. Surgery 21, 887-911(1930).--When kept at room temp., 3% solns. of tribromoethanol are stable toward hydrolysis for 24-48 hrs. I t has practically the same mar
gin of safety as other commonly used anesthetics,. e., V-1/ of the fatal dose. With
proper precautions, 0.1 g. per kg. body wt. can be safely given. It is useful, given
intravenously, in very short operations, as it gives quick pleasant induction and re
covery without gastro-intestinal disturbance.
J ohn T. M yers
The toxicity of atmospheres containing hydrocyanic acid gas. J oseph Barcroft.
A Hyg- 31, 1-34(1931).--The sp. power of HCN gas to increase the total ventilation is an important factor in detg. the sp. toxicity of the gas. Man is relatively insusceptible
to the inhalation of HCN. The time of exposure sufficient for collapse is about one
third of the fatal period of exposure. The extreme susceptibility of the canary makes
it very valuable as an indicator of lethal concns. where a chem. indicator is not available.
Pigeons are as good since they vomit at the lethal concn. for the canary, although their
lethal concn. is about twice as great. Treatment consists of artificial respiration, and
the administration of glucose and nitrites.
J ohn T. M yers
Experimental dust inhalation in guinea pigs. F. Haynes. J. Hyg. 31, 96-123
(1931).--Most inhaled particles contain sol. matter at least to a small extent. The
solute may be harmlessly active or toxic. If harmless the cell is stimulated to detach itself from the alveolar wall and to remove the dust. If toxic the solute affects the
viability of the phagocyte which becomes less able to detach itself. At the same time the solute diffuses into the neighboring tissues with irritation to them and subsequent fibrosis. The more sol. form of a substance causes the greater damage; hence the solute has much to do with extent of damage. Si is the dust par excellence in predisposing
to tuberculosis. The harmful effects of sol. Si may be neutralized by simultaneous
administration of basic dusts as Al(OH), or MgCO, although the latter are harmful
when inhaled alone. It is suggested that the respective solutes combine to form
monosilicates which are harmless.
J ohn T. M yers
Asbestosis bodies in the sputum: a study of specimens from fifty workers in an asbestos mill. K. W. Simson and A. Sutherland Strachan. / . Path. Bact. 34, 1-4
(1931).--The inhalation of asbestos dust in high concns. leads to the appearance of asbestosis bodies in 48 out of 50 workers examd. The sputum is always mucoid in
character. It may resemble egg albumin. The bodies seem to be the result of depo
sition on the asbestos fiber of an Fe-contg. substance elaborated by the cell. No tubercle
bacilli were found in any of these cases.
J ohn T. M yers
Experimental liver necrosis from shale oil. Cyril J. Polson. J. Path. Bact. 34,
5-12(1931).--Liver necrosis was produced in rabbits and rats by the intraperitoneal injection of shale oil. By graduating the doses it is possible to produce all stages from
acute necrosis to cirrhosis. The poisonous action of the non-carcinogenic residue of shale oil is very slight. The liver was not thus affected in other animals. J. T. M.
The effect of oils on gastric secretion and motility. W. Morrell R oberts. Quart. J. Med. 24, 133-52(1931).--The efficiency of oils in inhibiting gastric secretion
appears to bear some relationship to the degree of satn. of the constituent fatty acids, less satd. oils being more efficient. The relationship between efficiency and sp. gr.
and viscosity is less significant. Of related substances, only free fatty acids show in
hibitory properties. Oil diminishes the response of the stomach to food or other sub stances but not to the effect of histamine. Oil inhibits both psychical and chem. stimu
lation of secretions. Its effect occurs almost entirely after it leaves the stomach. It diminishes the motility of achlorhydria. The effect on gastric motility is not secondary
to its effect on secretion. It seems necessary to assume that oil after absorption exerts
some restraining influence on the gastric cells and the motility, or that it leads to the formation or the liberation of some substance which acts in a similar manner.
J ohn T. M yers Cholagog action of a few derivatives of the aliphatic series of low molecular weight.
Etienne Chabrol, R. Charonnat, M. M aximin and R. Waitz. Compt. rend. soc. biol.
106, 15-6(1931).--A study was made of the effects on the cholagog action caused by substituting various groups and atoms for the Cl and the COsH group in ChCCC^H. Con
clusions: (1) The cholagog action disappears when the COjH group is replaced by an amide, ale. or Me group. (2) BrCHjCOjH causes an immediate and powerful cholagog
action, but its toxicity is too great for a prolonged study; glycine in a 2-gr. dose doubled the biliary flow during 1 hr. with a 17.5 kg. dog but was completely inactive in doses of 1 gr. with other dogs; glycolic, cyanoacetic, glyoxalic and malonic acids had no