Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where George E. Burrows is active.

Publication


Featured researches published by George E. Burrows.


Toxicology and Applied Pharmacology | 1982

Effects of oxygen on the antagonism of cyanide intoxication: cytochrome oxidase, in vitro.

Gary E. Isom; George E. Burrows; James L. Way

Since oxygen was reported to be an effective cyanide antagonist in vivo, particularly in the presence of the classic antidotal combination of sodium nitrite and sodium thiosulfate, in vitro studies were initiated in an attempt to investigate the mechanism of oxygen-mediated cyanide antagonism. The effect of oxygen on cyanide-inhibited cytochrome oxidase with and without cyanide antagonist(s) was investigated in a purified membraneous enzyme system prepared from rat liver mitochondria. Cyanide produced a concentration dependent inhibition of cytochrome oxidase, and 100% oxygen did not alter the inhibition produced by KCN either in the presence or absence of sodium thiosulfate. However, the addition of sodium thiosulfate and rhodanese to the assay reactivated the cyanide-inhibited cytochrome oxidase. Kinetic analysis indicated rhodanese competes with cytochrome oxidase for cyanide, and oxygen had no effect on this coupled reaction. In conclusion, the in vivo antidotal properties of oxygen cannot be attributed to oxygen-mediated reactivation of cyanide-inhibited cytochrome oxidase or an oxygen-mediated acceleration of rhodanese detoxification.


Veterinary Clinics of North America-food Animal Practice | 1991

Therapy of bovine bacterial pneumonia

Cyril R. Clarke; George E. Burrows; Trevor R. Ames

Practical strategies for developing rational therapeutic regimens based on in vitro sensitivity and pharmacokinetic disposition are presented. Special attention is given to Pasteurella haemolytica, which is regarded as the most frequent cause of bovine bacterial pneumonia. Bacterial-dependent and host-dependent causes of therapeutic failure and potentially valuable novel therapies and drug combinations are considered.


Toxicology and Applied Pharmacology | 1983

Effect of chlorpromazine on cyanide intoxication

Alan Kong; Anna Shen; George E. Burrows; Diane Sylvester; Gary E. Isom; James L. Way

Previous reports from our laboratory indicated that prophylactic protection against cyanide intoxication in mice can be enhanced by administration of chlorpromazine when it is given with sodium thiosulfate. The mechanism of potentiation of sodium thiosulfate by chlorpromazine was studied alone and in combination with sodium nitrite. Although chlorpromazine was found to induce a hypothermic response, the mechanism of enhancement of the antagonism of cyanide by chlorpromazine does not correlate with the hypothermia produced. Various other possible mechanisms were investigated, such as rate of methemoglobin formation, enzymatic activity of rhodanese and cytochrome oxidase, and alpha-adrenergic blockade. The alpha-adrenergic blocking properties of chlorpromazine may provide a basis for its antidotal effect, since this protective effect can be reversed with an alpha-agonist, methoxamine.


Journal of Veterinary Diagnostic Investigation | 1989

In vitro assessment of the efficacy of erythromycin in combination with oxytetracycline or spectinomycin against Pasteurella haemolytica

George E. Burrows; Patty Ewing

The effects of combining erythromycin (Ery) with oxytetracycline (Oxy) or spectinomycin (Sp) on Pasteurella haemolytica were evaluated in vitro using the chessboard (checkerboard) technique. These combinations were selected because all are drugs widely used in bovine respiratory disease treatment, and they represent possible sequential or complementary mechanisms of action. Using the recommended breakpoints of >4 μg/ml for Ery, 16 μl for Oxy, and 32 μl for Sp, of the 33 P. haemolytica isolates, 32 were resistant to Oxy, 27 to Sp, and 14 to Ery. Based on the fractional inhibitory concentration index, Ery and Oxy in combination were synergistic or additive against 32 of 33 isolates. The combination of Ery and Sp was synergistic or additive against 27 of 33 isolates. No instances of antagonism were seen. When the effects were considered within the context of therapeutically achievable serum/tissue concentrations, the effects of Ery and Oxy in combination were only marginal. Thus, against P. haemolytica isolates, Ery and Sp appeared to represent an effective antimicrobial combination, whereas Ery and Oxy were only of marginal efficacy as a combination.


Journal of Toxicology and Environmental Health | 1982

Effect of antagonists on the physiologic disposition of sodium cyanide

George E. Burrows; David H. W. Liu; Gary E. Isom; James L. Way

Attempts were made to evaluate the effects of pretreatment with air and oxygen either alone or in various combinations with sodium nitrite and/or sodium thiosulfate on the physiological disposition of 14C-labeled sodium cyanide in mice. The radioactive respiratory excretion was studied by radiorespirometry, and the effects of various combinations of cyanide antagonists were compared. Oxygen either alone or in combination with sodium thiosulfate significantly enhanced the respiratory excretion when compared with air. Sodium thiosulfate accelerated the initial rate, but not the total amount of radioactivity excreted. The cumulative recovery of radioactive gases was significantly greater with groups receiving oxygen either alone or with sodium thiosulfate. When sodium nitrite was employed as an antidote either alone or with sodium thiosulfate, no difference in the respiratory excretion was noted between air and oxygen. The use of the sodium nitrite-sodium thiosulfate combination either with air or oxygen resulted in a marked decrease in the initial rate as well as the total amount of respiratory radioactivity excreted. No significant differences between various experimental groups were noted in the total amount of urinary radioactivity excreted or the total body retention of radioactivity.


Toxicon | 1981

The effect of proteinase inhibitors on experimentally induced equine E. coli endotoxemia

George E. Burrows

Abstract Trasylol (10,000 Kallikrein Inactivator Units) and soybean trypsin inhibitor (10 mg/kg) were evaluated for possible therapeutic effects in an equine i.p. model of E. coli endotoxemia. Although trasylol reduced or delayed the pyrexia and β-glucuronidasemia and soybean trypsin inhibitor delayed the β-glucuronidasemia associated with endotoxemia, neither produced a significant reduction in the overall severity of the equine response to E. coli endotoxin.


Journal of Veterinary Pharmacology and Therapeutics | 1996

Penetration of parenterally administered ceftiofur into sterile vs. Pasteurella haemolytica-infected tissue chambers in cattle

Cyril R. Clarke; S. A. Brown; R. N. Streeter; J. M. Clarke; P. J. Hamlow; J. K. Callahan; V. L. Hubbard; A. K. Speedy; George E. Burrows


Journal of Veterinary Pharmacology and Therapeutics | 1984

Methylene blue: effects and disposition in sheep.

George E. Burrows


Journal of Veterinary Pharmacology and Therapeutics | 1987

Comparative pharmacokinetics of gentamicin, neomycin and oxytetracycline in newborn calves

George E. Burrows; P. B. Barto; B. Martin


Journal of Pharmacology and Experimental Therapeutics | 1973

EFFECT OF OXYGEN ON CYANIDE INTOXICATION. V. PHYSIOLOGIC EFFECTS

George E. Burrows; David H. W. Liu; James L. Way

Collaboration


Dive into the George E. Burrows's collaboration.

Top Co-Authors

Avatar

James L. Way

Washington State University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

David H. W. Liu

Washington State University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge