Українська English

ISSN 2522-9028 (Print)
ISSN 2522-9036 (Online)
DOI: https://doi.org/10.15407/fz

Fiziologichnyi Zhurnal

is a scientific journal issued by the

Bogomoletz Institute of Physiology
National Academy of Sciences of Ukraine

Editor-in-chief: V.F. Sagach

The journal was founded in 1955 as
1955 – 1977 "Fiziolohichnyi zhurnal" (ISSN 0015 – 3311)
1978 – 1993 "Fiziologicheskii zhurnal" (ISSN 0201 – 8489)
1994 – 2016 "Fiziolohichnyi zhurnal" (ISSN 0201 – 8489)
2017 – "Fiziolohichnyi zhurnal" (ISSN 2522-9028)

Fiziol. Zh. 2024; 70(6): 3-8


Action potentials of the superior cervical ganglion neurons in the rats in diabetes mellitus

A.O. Nastenko, H.E. Purnyn, S.A. Fedulova, N.S. Veselovsky

    Bogomoletz Institute of Physiology National Academy of Sciences of Ukraine, Kyiv, Ukraine
DOI: https://doi.org/10.15407/fz70.06.003


Abstract

It’s well known that sympathetic and sensory neurons are affected in the early stages of diabetes mellitus (DM). However, the functional disorders that occur in neurons of the superior cervical ganglion (SCG) under the conditions of DM remain insufficiently studied. Therefore, the aim of this study was to evaluate the effect of streptozotocin-induced diabetes mellitus (DM) of the rats on action potentials (AP) recorded in the superior cervical ganglion`s (SCG) neurons. Rats with blood sugar level more than 30 mM were taken into experiment. The SCG of healthy control rats (n=12), rats at week 4 (n=9), and rats at week 12 after streptozotocin injection (n=9) were studied in vitro. AP of the SCG neurons were registered by the microelectrode technique. Neurons of the SCG were stimulated directly with 150 ms depolarizing current in pulse of 100 pA. The AP parameters of 36 SCG neurons of control rats were alternately compared with the corresponding AP parameters of 22 neurons of rats at week 4 and 30 SCG neurons of rats at week 12 after streptozotocin injection. The data obtained demonstrate that the AP amplitude and overshoot of AP, maximum rise and fall rates, and afterhyperpolarization amplitude significantly decreased at 12 weeks after DM induction. At the same time, the rheobase value significantly increased, this may indicates decreasing of the neurons plasma membrane excitability. Only the AP maximum rate of fall decreased statistically significant at week 4, the maximum rate of rise had an insignificant tendency to decrease at that time. However, the resting membrane potential and excitation threshold didn’t change even at 12 weeks after the injection. Thus, functional disorders of rat SCG neurons were appeared at a quite late stage of DM. The differences in AP parameters may result from neurons’ membrane ionic conductivity alterations, decreasing of its excitability and reducing ion channels efficiency in later stages of DM. This suggests that SCG is an important target of pathophysiological disorders caused by DM.

Keywords: superior cervical ganglion; diabetic neuropathy; streptozotocin-induced diabetes; action potential; membrane conductivity.

References

  1. Snyder MJ, Gibbs LM, Lindsay TJ. Treating painful diabetic peripheral neuropathy: An update. Am Fam Phys. 2016 Aug 1;94(3):227-34.
  2. Nastenko AO, Purnyn HE, Veselovsky NS. Physiological functions disorders of the superior cervical ganglion neurons in diabetes mellitus. Fiziol Zh. 2022;68(1):74-86. CrossRef
  3. Radenković M, Stojanović M, Prostran M. Experimental diabetes induced by alloxan and streptozotocin: The current state of the art. J Pharm Toxicol Method. 2016 Mar-Apr;78:13-31. Savastano LE, Castro AE, Fitt MR, Rath MF, Romeo HE, Muñoz EM. A standardized surgical technique for rat superior cervical ganglionectomy. J Neurosci Method. 2010 Sep 30;192(1):22-33. CrossRef PubMed
  4. Campanucci V, Krishnaswamy A, Cooper E. Diabetes depresses synaptic transmission in sympathetic ganglia by inactivating nAChRs through a conserved intracellular cysteine residue. Neuron. 2010 Jun 24;66(6):827-34. CrossRef PubMed
  5. Cameron NE, Cotter MA. Diabetes causes an early reduction in autonomic ganglion blood flow in rats. J Diabet Complicat. 2001 Jul-Aug;15(4):198-202. CrossRef PubMed
  6. Silva-Dos-Santos NM, Oliveira-Abreu K, Moreira-Junior L, Santos-Nascimento TD, Silva-Alves KSD, Coelhode-Souza AN, Ferreira-da-Silva FW, Leal-Cardoso JH. Diabetes mellitus alters electrophysiological properties in neurons of superior cervical ganglion of rats. Brain Res. 2020 Feb15;1729:146599. CrossRef PubMed
  7. Krarup C, Moldovan M. Nerve conduction and excitability studies in peripheral nerve disorders. Current Opin Neurol. 2009 Oct;22(5):460-6. CrossRef PubMed
  8. Pathak D, Guan D, Foehring RC. Roles of specific Kv channel types in repolarization of the action potential in genetically identified subclasses of pyramidal neurons in mouse neocortex. J Neurophysiol. 2016 May 1;115(5):2317-29. CrossRef PubMed PubMedCentral
  9. Airapetian SN. Mechanism of trace hyperpolarization of the action potential of snail giant neurons. Biofizika. 1975 May-Jun;20(3):462-6.
  10. Benarroch EE. Na+, K+-ATPase: functions in the nervous system and involvement in neurologic disease. Neurology. 2011 Jan 18;76(3):287-93. CrossRef PubMed
  11. Greene DA, Mackway AM. Decreased myo-inositol content and Na+-K+-ATPase activity in superior cervical ganglion of STZ-diabetic rat and prevention by aldose reductase inhibition. Diabetes. 1986 Oct;35(10):1106-8. CrossRef PubMed
  12. Krishnaswamy A, Cooper E. Reactive oxygen species inactivate neuronal nicotinic acetylcholine receptors through a highly conserved cysteine near the intracellular mouth of the channel: implications for diseases that involve oxidative stress. J Physiol. 2012 Jan 1;590(1):39-47. CrossRef PubMed PubMedCentral
  13. Tomlinson DR, Gardiner NJ. Glucose neurotoxicity. Nat Rev Neurosci. 2008 Jan;9(1):36-45. CrossRef PubMed

© National Academy of Sciences of Ukraine, Bogomoletz Institute of Physiology, 2014-2025.