Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1979 Mar;76(3):1501–1505. doi: 10.1073/pnas.76.3.1501

A peptide as a possible transmitter in sympathetic ganglia of the frog.

Y N Jan, L Y Jan, S W Kuffler
PMCID: PMC383282  PMID: 35789

Abstract

A search was made in sympathetic ganglia of the bullfrog for a noncholinergic, nonaminergic transmitter that is released by a distinct group of preganglionic axons. These initiate a late slow excitatory postsynaptic potential which lasts for many minutes. The most promising candidate for the role of transmitter is a peptide that resembles luteinizing hormone-releasing hormone (LHRH; luliberin). The reasons are: (i) LHRH (1 muM) and some of its analogs cause a slow depolarization of ganglion cells. (ii) Radioimmunoassays established that 100-800 pg of a LHRH-like substance is contained in the lumbar chain of sympathetic ganglia. (iii) The LHRH-like material is specifically distributed in those spinal nerves that contain axons that initiate the slow noncholinergic synaptic responses. (iv) Five days after ipsilateral preganglionic axons are cut, 95% of the LHRH-like substance disappears from ganglia, while the LHRH immunoreactivity triples in the spinal nerves proximal to the cut region. (v) About 0.6% of the LHRH-like material within ganglia can be collected from the perfusate after 30 min of incubation in isotonic KC1; this release is Ca dependent. (vi) The candidate for transmitter has several chemical characteristics of a peptide and has a Mr near 1000.

Full text

PDF
1501

Images in this article

Selected References

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

  1. Arimura A., Sato H., Kumasaka T., Worobec R. B., Debeljuk L., Dunn J., Schally A. V. Production of antiserum to LH-releasing hormone (LH-RH) associated with gonadal atrophy in rabbits: development of radioimmunoassays for LH-RH. Endocrinology. 1973 Nov;93(5):1092–1103. doi: 10.1210/endo-93-5-1092. [DOI] [PubMed] [Google Scholar]
  2. ECCLES R. M. Intracellular potentials recorded from a mammalian sympathetic ganglion. J Physiol. 1955 Dec 29;130(3):572–584. doi: 10.1113/jphysiol.1955.sp005428. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Feldberg W., Gaddum J. H. The chemical transmitter at synapses in a sympathetic ganglion. J Physiol. 1934 Jun 9;81(3):305–319. doi: 10.1113/jphysiol.1934.sp003137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Guillemin R. Peptides in the brain: the new endocrinology of the neuron. Science. 1978 Oct 27;202(4366):390–402. doi: 10.1126/science.212832. [DOI] [PubMed] [Google Scholar]
  5. Hökfelt T., Elfvin L. G., Schultzberg M., Goldstein M., Nilsson G. On the occurrence of substance P-containing fibers in sympathetic ganglia: immunohistochemical evidence. Brain Res. 1977 Aug 19;132(1):29–41. doi: 10.1016/0006-8993(77)90704-1. [DOI] [PubMed] [Google Scholar]
  6. Iversen L. L., Jessell T., Kanazawa I. Release and metabolism of substance P in rat hypothalamus. Nature. 1976 Nov 4;264(5581):81–83. doi: 10.1038/264081a0. [DOI] [PubMed] [Google Scholar]
  7. Katayama Y., North R. A. Does substance P mediate slow synaptic excitation within the myenteric plexus? Nature. 1978 Jul 27;274(5669):387–388. doi: 10.1038/274387a0. [DOI] [PubMed] [Google Scholar]
  8. Libet B., Chichibu S., Tosaka T. Slow synaptic responses and excitability in sympathetic ganglia of the bullfrog. J Neurophysiol. 1968 May;31(3):383–395. doi: 10.1152/jn.1968.31.3.383. [DOI] [PubMed] [Google Scholar]
  9. Libet B., Kobayashi H. Adrenergic mediation of slow inhibitory postsynaptic potential in sympathetic ganglia of the frog. J Neurophysiol. 1974 Jul;37(4):805–814. doi: 10.1152/jn.1974.37.4.805. [DOI] [PubMed] [Google Scholar]
  10. Libet B., Tosaka T. Slow inhibitory and excitatory postsynaptic responses in single cells of mammalian sympathetic ganglia. J Neurophysiol. 1969 Jan;32(1):43–50. doi: 10.1152/jn.1969.32.1.43. [DOI] [PubMed] [Google Scholar]
  11. McMahan U. J., Kuffler S. W. Visual identification of synaptic boutons on living ganglion cells and of varicosities in postganglionic axons in the heart of the frog. Proc R Soc Lond B Biol Sci. 1971 Apr 27;177(1049):485–508. doi: 10.1098/rspb.1971.0044. [DOI] [PubMed] [Google Scholar]
  12. Neild T. O. Slowly-developing depolarization of neurones in the guinea-pig inferior mesenteric ganglion following repetitive stimulation of the preganglionic nerves. Brain Res. 1978 Jan 27;140(2):231–239. doi: 10.1016/0006-8993(78)90457-2. [DOI] [PubMed] [Google Scholar]
  13. Nett T. M., Adams T. E. Further studies on the radioimmunoassay of gonadotropin-releasing hormone: effect of radioiodination, antiserum and unextracted serum on levels of immunoreactivity in serum. Endocrinology. 1977 Oct;101(4):1135–1144. doi: 10.1210/endo-101-4-1135. [DOI] [PubMed] [Google Scholar]
  14. Nett T. M., Akbar A. M., Niswender G. D., Hedlund M. T., White W. F. A radioimmunoassay for gonadotropin-releasing hormone (Gn-RH) in serum. J Clin Endocrinol Metab. 1973 May;36(5):880–885. doi: 10.1210/jcem-36-5-880. [DOI] [PubMed] [Google Scholar]
  15. Nishi S., Koketsu K. Early and late after discharges of amphibian sympathetic ganglion cells. J Neurophysiol. 1968 Jan;31(1):109–121. doi: 10.1152/jn.1968.31.1.109. [DOI] [PubMed] [Google Scholar]
  16. Nishi S., Soeda H., Koketsu K. Studies on sympathetic B and C neurons and patterns of pregnaglionic innervation. J Cell Physiol. 1965 Aug;66(1):19–32. doi: 10.1002/jcp.1030660103. [DOI] [PubMed] [Google Scholar]
  17. Otsuka M., Takahashi T. Putative peptide neurotransmitters. Annu Rev Pharmacol Toxicol. 1977;17:425–439. doi: 10.1146/annurev.pa.17.040177.002233. [DOI] [PubMed] [Google Scholar]
  18. Schally A. V. Aspects of hypothalamic regulation of the pituitary gland. Science. 1978 Oct 6;202(4363):18–28. doi: 10.1126/science.99816. [DOI] [PubMed] [Google Scholar]
  19. Takahashi T., Otsuka M. Regional distribution of substance P in the spinal cord and nerve roots of the cat and the effect of dorsal root section. Brain Res. 1975 Apr 4;87(1):1–11. doi: 10.1016/0006-8993(75)90774-x. [DOI] [PubMed] [Google Scholar]
  20. Weight F. F., Padjen A. Acetylcholine and slow synaptic inhibition in frog sympathetic ganglion cells. Brain Res. 1973 May 30;55(1):225–228. doi: 10.1016/0006-8993(73)90506-4. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES