Ritodrine and cyclopropane interaction

Ritodrine-Induced Hypokalemia

A 31-year-old woman presented with chest discomfort in the 22nd week of pregnancy. She had been treated with an intravenous infusion of ritodrine hydrochloride (0.25 mg/min) for preterm labor the prior day. On physical examination, the body temperature was 36.3°C, the blood pressure was 117/68 mmHg, the pulse was 96 beats/min, and the respiratory rate was 20 breaths/min. Electrocardiography (EC...

Cyclopropane Anæsthesia

TLHIS paper is based on my experience of one thousand cases of cyclopropane anaesthesia personally conducted by me since October, 1938, both in hospital and in private. But before discussing these it might be convenient for me to mention here something about the drug itself. HISTORY. Cyclopropane was first isolated in Germany in 1882 by Freund, who also demonstrated its chemical structure, C 3H...

Cyclopropane Anesthesia

Biosynthesis of Cyclopropane Compounds

Oleic acid was converted to dihydrosterculic acid (9,10methyleneoctadecanoic acid) by Lactobacillus arabinosus cells. This was established by the mass spectra of branched chain esters formed by reductive opening of the cyclopropane ring of the corresponding cyclopropane fatty esters. The mass spectra allowed unambiguous assignment of the ring location to position 9,10. Oleic acid-9,10-d2 was co...

Biosynthesis of Cyclopropane Compounds

Several natural and synthetic phospholipids can serve as substrates for the cyclopropane synthetase enzyme of Closfridium bufyricum. The conditions for optimum substrate effectiveness vary with the substrate; e.g. an anionic surfaceactive agent is necessary with phosphatidylethanolamine, while divalent cations stimulate the rate of reaction with anionic phospholipids. These variable conditions ...