Exp Clin Endocrinol Diabetes 2015; 123(05): 272-281
DOI: 10.1055/s-0035-1547258
Article
© Georg Thieme Verlag KG Stuttgart · New York

Analysis of Heart Rate Variability and Cardiac Autonomic Nerve Remodeling in Streptozotocin-induced Diabetic Rats

X. Li*
1   Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
Y.-H. Jiang*
1   Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
P. Jiang
2   Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
H.-Q. Lin
1   Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
J.-L. Yang
2   Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
D.-f. Ma
2   Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
X. Wang
2   Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
,
C.-H. Yang
1   Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Ji’nan, Shandong, P. R.China
› Author Affiliations
Further Information

Publication History

received 25 September 2014
first decision 12 February 2015

accepted 18 February 2015

Publication Date:
21 April 2015 (online)

Abstract

Background: Diabetes mellitus (DM) is associated with both cardiovascular and autonomic nervous system dysfunction. Spectral analysis of heart rate variability (HRV) can be used to monitor changes in response to autonomic innervation and stimulation of the heart. In this study, conducted in a rat model of diabetes, HRV and changes in associated neurotransmitters and neurotrophic factors in the right atrium (RA) were monitored.

Methods: Diabetes was induced by streptozotocin (STZ) (60 mg/kg) in male Wistar rats, and HRV data were collected for 10 weeks by telemetry. Time and frequency domains of HRV data were analyzed using established metrics. The levels of various neural enzymes in the RA were determined by enzyme-linked immunosorbent assay (ELISA) and immunofluorescence to characterize autonomic nerve remodeling. Insulin and methycobal were used to block the effects of STZ.

Results: HRV parameters reflecting parasympathetic tone (SDNN, RMSSD and HF domains) sharply decreased in the first 3 weeks after STZ administration; measures of sympathetic tone (SDANN) increased. After a series of adjustments, cardiac autonomic nerve innervation reached a new equilibrium, with a dominance of sympathetic tone. RA levels of tyrosine hydroxylase (TH) increased, and choline acetyltransferase (ChAT) decreased, indicating autonomic nerve remodeling. Levels of growth associated protein-43 (GAP43) and nerve growth factor (NGF) increased during the period of diabetes-induced cardiac-nerve damage; however, the level of ciliary neurotrophic factor (CNTF) decreased. The physical condition and indexes of rats were normalized in different degree after administration of the insulin and methycobal, but not completely recovered.

Conclusion: STZ-induced diabetes was associated with cardiac autonomic nerve dysfunction at both the organ and molecular levels. Parasympathetic nerves exhibited severe damage and/or weak recovery; remodeling of sympathetic nerves predominated during 10-weeks of STZ-induced diabetes.

* These authors contributed equally to this work and are both first authors.


 
  • References

  • 1 Kawano H, Okada R, Yano K. Histological study on the distribution of autonomic nerves in the human heart. Heart Vessels 2003; 18: 32-39
  • 2 From AM, Scott CG, Chen HH. The development of heart failure in patients with diabetes mellitus and pre-clinical diastolic dysfunction a population-based study. J Am Coll Cardiol 2010; 55: 300-305
  • 3 Whaley-Connell A, Habibi J, Panfili Z et al. Angiotensin II activation of mTOR results in tubulointerstitial fibrosis through loss of N-cadherin. Am J Nephrol 2011; 34: 115-125
  • 4 Kleiger RE, Stein PK, Bosner MS et al. Time domain measurements of heart rate variability. Cardiol Clin 1992; 10: 487-498
  • 5 Lee HW, Han TH, Yi KJ et al. Time course of diurnal rhythm disturbances in autonomic function of rats with myocardial infarction. Auton Neurosci 2013; 179: 28-36
  • 6 Zulfiqar U, Jurivich DA, Gao W et al. Relation of high heart rate variability to healthy longevity. Am J Cardiol 2010; 105: 1181-1185
  • 7 Cygankiewicz I, Zareba W. Heart rate variability. Handb Clin Neurol 2013; 117: 379-393
  • 8 Aubert AE, Ramaekers D, Beckers F et al. The analysis of heart rate variability in unrestrained rats. Validation of method and results. Comput Methods Programs Biomed 1999; 60: 197-213
  • 9 Howarth FC, Jacobson M, Naseer O et al. Short-term effects of streptozotocin-induced diabetes on the electrocardiogram, physical activity and body temperature in rats. Exp Physiol 2005; 90: 237-245
  • 10 Mabe AM, Hoover DB. Structural and functional cardiac cholinergic deficits in adult neurturin knockout mice. Cardiovasc Res 2009; 82: 93-99
  • 11 Otake H, Suzuki H, Honda T et al. Influences of autonomic nervous system on atrial arrhythmogenic substrates and the incidence of atrial fibrillation in diabetic heart. Int Heart J 2009; 50: 627-641
  • 12 Schaan BD, Dall’Ago P, Maeda CY et al. Relationship between cardiovascular dysfunction and hyperglycemia in streptozotocin-induced diabetes in rats. Braz J Med Biol Res 2004; 37: 1895-1902
  • 13 Wang Y, Xue M, Xuan YL et al. Mesenchymal stem cell therapy improves diabetic cardiac autonomic neuropathy and decreases the inducibility of ventricular arrhythmias. Heart Lung Circ 2013; 22: 1018-1025
  • 14 Yang B, Chon KH. Assessment of diabetic cardiac autonomic neuropathy in type I diabetic mice. Conf Proc IEEE Eng Med Biol Soc 2011; 2011: 6560-6563
  • 15 Chen PS, Chen LS, Cao JM et al. Sympathetic nerve sprouting, electrical remodeling and the mechanisms of sudden cardiac death. Cardiovasc Res 2001; 50: 409-416
  • 16 Cao JM, Chen LS, KenKnight BH et al. Nerve sprouting and sudden cardiac death. Circ Res 2000; 86: 816-821
  • 17 Hiltunen JO, Arumäe U, Moshnyakov M et al. Expression of mRNAs for neurotrophins and their receptors in developing rat heart. Circ Res 1996; 79: 930-939
  • 18 Kimura K, Ieda M, Fukuda K. Development, maturation, and transdifferentiation of cardiac sympathetic nerves. Circ Res 2012; 110: 325-336
  • 19 Lockhart ST, Mead JN, Pisano JM et al. Nerve growth factor collaborates with myocyte-derived factors to promote development of presynaptic sites in cultured sympathetic neurons. J Neurobiol 2000; 42: 460-476
  • 20 Korsching S, Thoenen H. Nerve growth factor in sympathetic ganglia and corresponding target organs of the rat: correlation with density of sympathetic innervation. Proc Natl Acad Sci USA 1983; 80: 3513-3516
  • 21 Zhou S, Chen LS, Miyauchi Y et al. Mechanisms of cardiac nerve sprouting after myocardial infarction in dogs. Circ Res 2004; 95: 76-83
  • 22 Schmid H, Forman LA, Cao X et al. Heterogeneous cardiac sympathetic denervation and decreased myocardial nerve growth factor in streptozotocin-induced diabetic rats: implications for cardiac sympathetic dysinnervation complicating diabetes. Diabetes 1999; 48: 603-608
  • 23 Wang X, Halvorsen SW. Reciprocal regulation of ciliary neurotrophic factor receptors and acetylcholine receptors during synaptogenesis in embryonic chick atria. J Neurosci 1998; 18: 7372-7380