Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Harold Blumberg"'
Autor:
Diane M. Slovak, Harold Blumberg
Publikováno v:
Life Sciences. 30:2115-2121
The alpha-adrenergic blocking agent, yohimbine, prevented the production of the morphine Straub tail reaction in mice, although on a mg dose basis it was only about 1 400 as potent as the narcotic antagonist naltrexone by subcutaneous injection. Like
Publikováno v:
Experimental Biology and Medicine. 105:35-38
Publikováno v:
The Journal of Nutrition. 16:317-324
Publikováno v:
Metabolism. 13:539-546
A series of 45 trials was carried out at 8 dosage levels on the nitrogen retaining effect of the synthetic anabolic steroid, Oxandrolone. At doses from 30 to 150 mg. the compound was maximally effective in nitrogen retention and progressively less ef
Autor:
Robert J. Myers, Harold Blumberg
Publikováno v:
Experimental Biology and Medicine. 35:79-84
Autor:
Aaron Arnold, Harold Blumberg
Publikováno v:
The Journal of Nutrition. 34:373-387
Publikováno v:
Experimental Biology and Medicine. 123:755-758
SummaryWhen the potent narcotic antagonist, naloxone, was injected subcutane-ously into mice and rats simultaneously with narcotic antagonist analgesics, naloxone counteracted the writhing test analgesic activity of the antagonists. Naloxone complete
Autor:
Harold Blumberg, Raymond E. Gardner
Publikováno v:
Experimental Biology and Medicine. 45:673-677
SummaryThe production of adenomatous stomach lesions of the rat, associated with heavy liver infestations of Cysticercus fasciolaris, is reported. The adenomatous stomach lesions have been produced in 3 different strains of rats.
Publikováno v:
Experimental Biology and Medicine. 118:763-766
SummaryIn a comparison of 6 narcotic antagonists, the analgesic potencies found on the phenylquinone writhing test, in both mice and rats, roughly paralleled the analgesic potencies reported in man. The analgesic potencies did not correlate with the
Publikováno v:
Journal of the American Pharmaceutical Association (Scientific ed.). 45:330-333
A comparison was made of aqueous tubocurarine and a repository D-tubocurarine chloride suspension (Tubadi®) for muscle relaxant effectiveness and toxicity in rabbits. As compared with intravenous aqueous tubocurarine on the basis of lethal dose, int