Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1971 Apr;214(1):159–171. doi: 10.1113/jphysiol.1971.sp009425

Noradrenaline release from isolated muscles of the nictitating membrane of the cat

S Z Langer, Marthe Vogt
PMCID: PMC1331828  PMID: 4324985

Abstract

1. When the splanchnic nerves were stimulated in the cat for periods of up to 2 hr, the amount of adrenaline taken up by the nictitating membrane was very small; the highest figure was 0·37 μg/g, corrected for losses.

2. The noradrenaline (NA) stores of the isolated medial muscle of the nictitating membrane were labelled with [3H]NA, and field stimulation of single muscles was carried out in a small organ bath. A stimulation period of 5 min with supramaximal shocks delivered at a frequency of 25/sec produced a mean release of NA into the bath fluid of 0·46 ± 0·13 μg/g (uncorrected). Phenoxybenzamine, 10 μg/ml., increased this figure by a factor of 2-3·6. When corrections were made for the amount of transmitter metabolized before it could be collected, 47% of the tissue content of NA were shown to be released during the 5 min stimulation of the normal membrane, and about 55% in the presence of phenoxybenzamine. Prolonged stimulation of a phenoxybenzamine-treated membrane was apt to lead to loss of tissue stores of NA.

3. Calculation of the degree of labelling of the NA in the tissue, and of NA released by stimulation, indicated that about 21% of endogenous NA had been replaced by labelled compound both in the tissue and in the overflow.

4. Transmitter release per pulse was estimated by applying 720-1330 shocks at frequencies of 4 or 6/sec to membranes exposed to phenoxybenzamine. Mean release of NA per shock and per g tissue was 1·3 ng (corrected for losses). This represents 3·5 × 10-4 of the tissue content determined at the end of the experiment.

Full text

PDF
159

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Folkow B., Häggendal J., Lisander B. Extent of release and elimination of noradrenaline at peripheral adrenergic nerve terminals. Acta Physiol Scand Suppl. 1967;307:1–38. [PubMed] [Google Scholar]
  2. Gillis C. N., Schneider F. H., Van Orden L. S., Giarman N. J. Biochemical and microfluorometric studies of norepinephrine redistribution accompanying sympathetic nerve stimulation. J Pharmacol Exp Ther. 1966 Jan;151(1):46–54. [PubMed] [Google Scholar]
  3. Haefely W., Hürlimann A., Thoenen H. Relation between the rate of stimulation and the quantity of noradrenaline liberated from sympathetic nerve endings in the isolated perfused spleen of the cat. J Physiol. 1965 Nov;181(1):48–58. doi: 10.1113/jphysiol.1965.sp007744. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. KIRPEKAR S. M., CERVONI P., FURCHGOTT R. F. Catecholamine content of the cat nicitating membrane following procedures sensitizing it to norepinephrine. J Pharmacol Exp Ther. 1962 Feb;135:180–190. [PubMed] [Google Scholar]
  5. Langer S. Z. The metabolism of (3H)noradrenaline released by electrical stimulation from the isolated nictitating membrane of the cat and from the vas deferens of the rat. J Physiol. 1970 Jul;208(3):515–546. doi: 10.1113/jphysiol.1970.sp009135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. STROMBLAD B. C. Effects of insulin on adrenaline and noradrenaline content of some rat tissues. Proc Soc Exp Biol Med. 1961 Nov;108:345–347. doi: 10.3181/00379727-108-26934. [DOI] [PubMed] [Google Scholar]
  7. STROMBLAD B. C., NICKERSON M. Accumulation of epinephrine and norepinephrine by some rat tissues. J Pharmacol Exp Ther. 1961 Nov;134:154–159. [PubMed] [Google Scholar]
  8. Stjärne L., Hedqvist P., Bygdeman S. Neurotransmitter quantum released from sympathetic nerves in cat's skeletal muscle. Life Sci. 1969 Feb 1;8(3):189–196. doi: 10.1016/0024-3205(69)90093-9. [DOI] [PubMed] [Google Scholar]
  9. Trendelenburg U., Draskóczy P. R., Pluchino S. The density of adrenergic innervation of the cat's nictitating membrane as a factor influencing the sensitivity of the isolated preparation to l-norepinephrine. J Pharmacol Exp Ther. 1969 Mar;166(1):14–25. [PubMed] [Google Scholar]
  10. VANOV S., VOGT M. CATECHOLAMINE-CONTAINING STRUCTURES IN THE HYPOGASTRIC NERVES OF THE DOG. J Physiol. 1963 Oct;168:939–944. doi: 10.1113/jphysiol.1963.sp007232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. VOGT M. The secretion of the denervated adrenal medulla of the cat. Br J Pharmacol Chemother. 1952 Jun;7(2):325–330. doi: 10.1111/j.1476-5381.1952.tb01329.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. VOGT M. Vasopressor, antidiuretic, and oxytocic activities of extracts of the dog's hypothalamus. Br J Pharmacol Chemother. 1953 Jun;8(2):193–196. doi: 10.1111/j.1476-5381.1953.tb00777.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES