Access the full text.
Sign up today, get DeepDyve free for 14 days.
R. Wadsworth (1973)
Abolition of neurally evoked motor responses of the vas deferens by 6-hydroxydopamine.European journal of pharmacology, 21 3
Kosterlitz Hw, Waterfield Aa, Berthoud (1973)
Assessment of the agonist and antagonist properties of narcotic analgesic drugs by their actions on the morphine receptor in the guinea pig ileum.Advances in biochemical psychopharmacology, 8 0
H. Blumberg, Dayton Hb (1973)
Naloxone, naltrexone, and related noroxymorphones.Advances in biochemical psychopharmacology, 8 0
Kosterlitz Kosterlitz, Waterfield Waterfield (1975)
In vitro models in the study of structure‐activity relationships of narcotic analgesicsA. Rev. Pharmac., 15
J. Hughes (1973)
Inhibition of noradrenaline release by lysergic acid diethylamideBritish Journal of Pharmacology, 49
(1972)
Morphine receptor in the myenteric plexus of the guinea - pig ileum
Hughes Hughes, Kosterlitz Kosterlitz, Leslie Leslie (1974)
Assessment of the agonist and antagonist activities of narcotic analgesic drugs by means of the mouse vas deferensBr. J. Pharmac., 51
N. Ambache, L. Dunk, J. Verney, M. Zar (1972)
Inhibition of post‐ganglionic motor transmission in vas deferens by indirectly acting sympathomimetic drugsThe Journal of Physiology, 227
T. Adler (1963)
Comparative potencies of codeine and its demethylated metabolites after intraventricular injection in the mouse.The Journal of pharmacology and experimental therapeutics, 140
E. Gyand, H. Kosterlitz (1966)
Agonist and antagonist actions of morphine-like drugs on the guinea-pig isolated ileum.British journal of pharmacology and chemotherapy, 27 3
John Furness (1974)
TRANSMISSION TO THE LONGITUDINAL MUSCLE OF THE GUINEA‐PIG VAS DEFERENS: THE EFFECT OF PRETREATMENT WITH GUANETHIDINEBritish Journal of Pharmacology, 50
J. Hughes, H. Kosterlitz, F. Leslie (1974)
Proceedings: Assessment of the agonist and antagonist activities of narcotic analgesic drugs by means of the mouse vas deferens.British journal of pharmacology, 51 1
H. Kosterlitz, A. Watt (1968)
Kinetic parameters of narcotic agonists and antagonists, with particular reference to N-allylnoroxymorphone (naloxone).British journal of pharmacology and chemotherapy, 33 2
D. Jacobowitz, G. Koelle (1965)
HISTOCHEMICAL CORRELATIONS OF ACETYLCHOLINESTERASE AND CATECHOLAMINES IN POSTGANGLIONIC AUTONOMIC NERVES OF THE CAT, RABBIT, AND GUINEA PIG.The Journal of pharmacology and experimental therapeutics, 148
M. Boadle-Biber, J. Hughes, R. Roth (1970)
Acceleration of noradrenaline biosynthesis in the guinea‐pig vas deferens by potassiumBritish Journal of Pharmacology, 40
H. Kosterlitz, A. Waterfield (1975)
In vitro models in the study of structure-activity relationships of narcotic analgesics.Annual review of pharmacology, 15
Taber Ri (1973)
Predictive value of analgesic assays in mice and rats.Advances in biochemical psychopharmacology, 8
Jeffery Hughes (1972)
Evaluation of mechanisms controlling the release and inactivation of the adrenergic transmitter in the rabbit portal vein and vas deferensBritish Journal of Pharmacology, 44
C. Pert, S. Snyder (1973)
Properties of opiate-receptor binding in rat brain.Proceedings of the National Academy of Sciences of the United States of America, 70 8
G. Henderson, J. Hughes, H. Kosterlitz (1997)
A new example of a morphine‐sensitive neuro‐effector junction: Adrenergic transmission in the mouse vas deferensBritish Journal of Pharmacology, 120
1 Morphine inhibits the electrically evoked (0.1‐0.15 Hz, 1 ms) contractions of the longitudinal muscle of the mouse vas deferens but not of the rabbit, guinea‐pig, rat, cat, hamster or gerbil. This effect is stereospecific and is antagonized by naloxone or naltrexone. 2 Normorphine is equiactive with morphine but its effects are more rapid in onset and decline. 3 In the mouse vas deferens, the resting outflow of tritium‐labelled catecholamines is unaffected by morphine. The electrically evoked outflow is depressed by morphine or normorphine in a dose‐dependent manner. The ID50 for inhibition of contraction and for depression of outflow is 0.5 μM. 4 The relative agonist potencies of compounds without antagonist component (codeine, pethidine, morphine, normorphine, heroin, levorphanol, Ba‐20227, etorphine) show good correlation with the relative agonist potencies determined in the guinea‐pig ileum and for analgesia in man. 5 For compounds with dual agonist and antagonist properties, the dose‐response curves for agonist activity are shallow. When the lowest concentrations giving a depression of the contraction of the mouse vas deferens are used, a good correlation is obtained with the guinea‐pig ileum. 6 The relative antagonist potencies of naloxone, nalorphine, levallorphan and cyclazocine agree well with those obtained in the guinea‐pig ileum; these, in turn, correlate well with the values obtained in the morphine‐dependent monkey. 7 The fact that the agonist effects of drugs with dual agonist and antagonist action show little or no dependence on concentration, makes the mouse vas deferens particularly suitable for the assay of antagonist activity. 8 As an assay preparation, the mouse vas deferens is less robust and consistent in its responses than the guinea‐pig ileum.
British Journal of Pharmacology – Wiley
Published: Mar 1, 1975
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.