Home LiteratureArticle Details
PMID: 4170546 Published · ppublish English Journal Article

Fine structural alterations associated with venom action on squid giant nerve fibers.

The Journal of cell biology ·Vol. 36 ·No. 2 ·1968-02-00 ·Pages 341-53

Martin R, Rosenberg P

Abstract

(1) Block of conduction and marked increase in permeability of the squid giant axon, when surrounded by adhering small nerve fibers, is caused by the venoms of cottonmouth, ringhals, and cobra snakes and by phospholipase A (PhA). This phenomenon is associated with a marked breakdown of the substructure of the Schwann sheath into masses of cytoplasmic globules. Low concentrations of these agents which render the axons sensitive to curare cause less marked changes in the structure of the sheath. (2) Rattlesnake venom, the direct lytic factor obtained from ringhals venom, and hyaluronidase caused few observable changes in structure, correlating with the inability of these agents to increase permeability. (3) Cottonmouth venom did not alter the structure of giant axons freed of all adhering small nerve fibers. This is in agreement with previous evidence that the venom effects are due to an action of lysophosphatides liberated as a result of PhA action. Cetyltrimethylammonium chloride, a cationic detergent, produces effects that resemble those of venom and PhA. (4) The results provide evidence that PhA is the component of the venoms that is responsible for their effects. It also appears that the Schwann cell and possibly the axonal membrane are the major permeability barriers in the squid giant axon.

MeSH Terms
Action Potentials Animals Axons/drug effects Cell Membrane Permeability/drug effects Curare/pharmacology Cytoplasm Extracellular Space Histocytochemistry Microscopy, Electron Mollusca Neural Conduction/drug effects Phospholipases/pharmacology Quaternary Ammonium Compounds/pharmacology Schwann Cells/drug effects Snakes Staining and Labeling Venoms/pharmacology
Chemicals
Quaternary Ammonium Compounds Venoms Curare Phospholipases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Martin R
Rosenberg P
References (22)
22 references, click to expand
  1. Reversible block of axonal conduction by curare after treatment with cobra venom.
    Biochem Pharmacol. 1961 Sep;8:192-206 PMID: 14493974
  2. Demonstration of phospholipid splitting as the factor responsible for increased permeability and block of axonal conduction induced by snake venom. I. Study of lobster axons.
    Biochim Biophys Acta. 1967 Sep 9;135(4):669-81 PMID: 6048249
  3. Effects of venoms on the squid giant axon.
    Toxicon. 1965 Nov;3(2):125-31 PMID: 5867067
  4. Ultrastructure of the prawn nerve sheaths. Role of fixative and osmotic pressure in vesiculation of thin cytoplasmic laminae.
    J Cell Biol. 1967 Aug;34(2):407-20 PMID: 4166578
  5. Chemical control of the permeability cycle in excitable membranes during electrical activity.
    Ann N Y Acad Sci. 1966 Jul 14;137(2):877-900 PMID: 5229835
  6. Demonstration of increased permeability as a factor in the effect of acetylcholine on the electrical activty of venom-treated axons.
    J Gen Physiol. 1963 May;46:1065-73 PMID: 13974908
  7. Penetration of sugars, steroids, amino acids, and other organic compounds into the interior of the squid giant axon.
    J Gen Physiol. 1965 Sep;49(1):47-56 PMID: 5862505
  8. THE STRUCTURE OF THE SCHWANN CELL AND ITS RELATION TO THE AXON IN CERTAIN INVERTEBRATE NERVE FIBERS.
    Proc Natl Acad Sci U S A. 1954 Sep;40(9):863-70 PMID: 16589576
  9. Penetration of acetylcholine into squid giant axons.
    Biochem Pharmacol. 1965 Dec;14(12):1765-72 PMID: 5880534
  10. INCREASED CHOLINESTERASE ACTIVITY OF INTACT CELLS CAUSED BY SNAKE VENOMS.
    Biochem Pharmacol. 1964 Aug;13:1157-65 PMID: 14222513
  11. Experimentally altered structure related to function in the lobster axon with an extrapolation to molecular mechanisms in excitation.
    J Cell Physiol. 1958 Aug;52(1):89-125 PMID: 13630981
  12. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.
    J Cell Biol. 1963 Apr;17:208-12 PMID: 13986422
  13. ABILITY OF VENOMS TO RENDER SQUID AXONS SENSITIVE TO CURARE AND ACETYLCHOLINE.
    Biochim Biophys Acta. 1963 Jul 23;75:104-15 PMID: 14060117
  14. Morphogenesis of the Schwann channels in the squid nerve.
    J Ultrastruct Res. 1963 Apr;8:197-205 PMID: 13997301
  15. HEMOLYSIS AND SPLITTING OF HUMAN ERYTHROCYTE PHOSPHOLIPIDS BY SNAKE VENOMS.
    Biochim Biophys Acta. 1964 Feb 24;84:60-73 PMID: 14124757
  16. FACTORS IN VENOMS LEADING TO BLOCK OF AXONAL CONDUCTION BY CURARE.
    Biochim Biophys Acta. 1963 Jul 23;75:116-28 PMID: 14060118
  17. A relation between non-esterified fatty acids in plasma and the metabolism of glucose.
    J Clin Invest. 1956 Feb;35(2):150-4 PMID: 13286333
  18. Contrast between osmium-fixed and permanganate-fixed toad spinal ganglia.
    J Cell Biol. 1963 Jan;16:143-57 PMID: 13990905
  19. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  20. Schwann cell and axon electrical potential differences. Squid nerve structure and excitable membrane location.
    J Gen Physiol. 1963 May;46:1047-64 PMID: 13997308
  21. Block of conduction by acetylcholine and d-tubocurarine after treatment of squid axon with cottonmouth moccasin venom.
    J Pharmacol Exp Ther. 1962 Aug;137:249-62 PMID: 14493975
  22. The ultrastructure of the giant nerve fibre of the squid: axon-Schwann cell relationship.
    J Ultrastruct Res. 1960 Jun;3:362-73 PMID: 13842312
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1968-02-00
Pages
341-53
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2107363
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]