Naunyn-Schmiedeberg's Archives of Pharmacology

, Volume 356, Issue 3, pp 356–363

Capsaicin-sensitive local sensory innervation is involved in pacing-induced preconditioning in rat hearts: role of nitric oxide and CGRP?

  • P. Ferdinandy
  • Tamás Csont
  • Csaba Csonka
  • Marianna Török
  • Mária Dux
  • József Németh
  • László I. Horváth
  • László Dux
  • Zoltán Szilvássy
  • Gábor Jancsó
Original article

DOI: 10.1007/PL00005062

Cite this article as:
Ferdinandy, P., Csont, T., Csonka, C. et al. Naunyn-Schmiedeberg's Arch Pharmacol (1997) 356: 356. doi:10.1007/PL00005062

Abstract

Among several mediators, nitric oxide (NO) and calcitonin gene-related peptide (CGRP) were suggested to be involved in the mechanism of preconditioning. We examined the possible role of the cardiac capsaicin-sensitive sensory innervation in pacing-induced preconditioning, as well as in the cardiac NO and CGRP content. Wistar rats were treated subcutaneously with capsaicin or its solvent in the sequence of 10, 30, and 50 mg/kg increasing single daily doses for 3 days to deplete neurotransmitters of the sensory innervation. Isolated hearts from both groups were then subjected to either preconditioning induced by three consecutive periods of pacing at 600 beats per minute for 5 min with 5 min interpacing periods, or time-matched non-preconditioning perfusion, followed by a 10-min coronary occlusion. NO content of left ventricular tissue samples was assayed by electron-spin resonance, and CGRP release was determined by radioimmunoassay. CGRP immunohistochemistry was also performed. In the non-preconditioned, solvent-treated group, coronary occlusion decreased cardiac output (CO) from 68.1 to 32.1 mL/min, increased left ventricular end-diastolic pressure (LVEDP) from 0.58 to 1.90 kPa, and resulted in 200 mU/min/g LDH release. Preconditioning significantly increased ischaemic CO to 42.9 mL/min (P < 0.05), decreased ischaemic LVEDP to 1.26 kPa (P < 0.05) and decreased LDH release to 47 mU/min/g (P < 0.05) in the solvent-treated group. Preconditioning did not confer protection in the capsaicin-pretreated group (ischaemic CO: 35.6 mL/min; LVEDP: 1.76 kPa; LDH 156 mU/min/g). Capsaicin-treatment markedly decreased cardiac NO content, CGRP release, and CGRP-immunoreactivity. Conclusions: (i) The presence of an intact local sensory innervation is a prerequisite to elicit pacing-induced preconditioning in the rat heart. (ii) A significant portion of cardiac basal NO content may be of neural origin. (iii) Release of NO and CGRP from capsaicin-sensitive nerves may be involved in the mechanism of pacing-induced preconditioning.

Key words PreconditioningRapid pacingCapsaicinNitric oxideElectron-spin resonanceCalcitoningene-related peptideImmunohistochemistryRat heart

Copyright information

© Springer-Verlag Berlin Heidelberg 1997

Authors and Affiliations

  • P. Ferdinandy
    • 1
  • Tamás Csont
    • 1
  • Csaba Csonka
    • 1
  • Marianna Török
    • 1
  • Mária Dux
    • 4
  • József Németh
    • 2
  • László I. Horváth
    • 3
  • László Dux
    • 1
  • Zoltán Szilvássy
    • 2
  • Gábor Jancsó
    • 4
  1. 1.Department of Biochemistry, Albert Szent-Györgyi University Medical School, H-6701 Szeged, P.O.Box 415, HungaryHU
  2. 2.Department of Medicine I, Albert Szent-Györgyi University Medical School, Korányi fasor 8, H-6720 Szeged, HungaryHU
  3. 3.Department of Biophysics, Biological Research Center, Temesvári krt. 44, H-6726 Szeged, HungaryHU
  4. 4.Department of Physiology, Albert Szent-Györgyi University Medical School, Dóm tér 9, H-6720 Szeged, HungaryHU