JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cohen, E. N.
Right arrow Articles by Hood, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cohen, E. N.
Right arrow Articles by Hood, N.
Journal of Pharmacology And Experimental Therapeutics, Vol. 157, Issue 1, 170-174, 1967
Copyright © 1967 by American Society for Pharmacology and Experimental Therapeutics


LOCALIZATION OF d-TUBOCURARINE-H3 AT THE MOTOR ENDPLATE

Ellis N. Cohen 1, Lucien J. Rubinstein 1, Aldo N. Corbascio 1, and Nancy Hood 1

1 Departments of Anesthesia and Pathology (Neuropathology), Stanford University School of Medicine, Palo Alto, California

The preparation of d-tubocurarine-H3 has permitted studies of its localization at the motor endplate through techniques of autoradiography. Five microcuries of d-tubocurarine-H3, equivalent to a dose of 0.6 µg/g b.wt., were injected into the tail vein of Swiss mice. The animals were sacrificed at the end of 1 min by decapitation and the diaphragm was removed. The latter was fixed in formalin vapor and sections were mounted after freezing in albumin. Cut sections (30 µ) were stained by a modification of the Koelle method adapted to prevent loss of the water-soluble d-tubocurarine. Autoradiography was performed with NTB3 emulsion. Development followed 10 to 21 days of exposure at 4°C. Localization of d-tubocurarine-H3 at the endplate was confirmed by light microscopy. Occasional evidence of strands of radioactivity leading into synaptic areas which contain dense radioactivity is suggestive of added preterminal localization of the drug.

Submitted on August 1, 1966
Accepted on February 7, 1967







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1967 by the American Society for Pharmacology and Experimental Therapeutics.