Neuropeptide depletion impairs postischemic recovery of the isolated rat heart

Role of substance p

Elena E. Ustinova, Dale Bergren, Harold D Schultz

Research output: Contribution to journalArticle

37 Citations (Scopus)

Abstract

Objectives: Ischemia of the myocardium stimulates cardiac sensory nerve endings resulting in the local release of neuropeptides. The significance of the release of neuropeptides, such as substance P (SP), for the function of the heart during ischemia and reperfusion is not known. We examined the effects of both chronic and acute neuropeptide depletion and of SP administration on contractile function and rhythmicity of the isolated rat heart during global ischemia and subsequent reperfusion. Methods: Experiments were conducted on the isolated perfused heart from vehicle and capsaicin-pretreated rats (100 mg/kg) to deplete neuropeptides from peripheral nerve terminals. The hearts were perfused with Krebs-Henseleit solution (95%O2 + 5% CO2, 37 °C, at constant pressure of 90 cmH2O). Left ventricular developed and diastolic pressures (LVDevP and LVEDP), heart rate (HR) and coronary flow (CF) were measured. Hearts were subjected to 20 min global no-flow ischemia and 30 min reperfusion. Results: Prior to interrupting coronary flow, LV pressures, HR and CF did not differ between vehicle and capsaicin-pretreated rats. However, throughout the reperfusion period, the recovery of LVDevP, HR and CF in hearts from capsaicin-pretreated rats was consistently less than in control hearts (P ` 0.05), and the incidence of fibrillation during reperfusion was higher (P ` 0.05). In other experiments, acute perfusion of isolated hearts with capsaicin (10−6 M) for 5 min before ischemia had a similar limiting effect during reperfusion. Administration of SP (10−6–10−9 M) to capsaicin-pretreated hearts before ischemia restored their ability to recover contractile function and CF during reperfusion. Administration of SP to untreated hearts before ischemia also improved their recovery above normal during reperfusion and decreased the incidence of fibrillation without affecting postischemic CF. The beneficial effects of SP were abolished by an NK-1 receptor antagonist, CP-96,345 (10−6 M). Conclusions: These data indicate that sensory neuropeptides play a role in protection of the isolated heart against ischemic damage and suggest a role of SP in the resistance of the myocardium to ischemia and reperfusion injury.

Original languageEnglish (US)
Pages (from-to)55-63
Number of pages9
JournalCardiovascular Research
Volume30
Issue number1
DOIs
StatePublished - Jan 1 1995

Fingerprint

Neuropeptides
Reperfusion
Substance P
Capsaicin
Ischemia
Heart Rate
Myocardium
Neurokinin-1 Receptors
Pressure
Incidence
Sensory Receptor Cells
Ventricular Pressure
Periodicity
Reperfusion Injury
Peripheral Nerves
Perfusion
Blood Pressure

Keywords

  • Capsaicin
  • Myocardial ischemia
  • Neuropeptides
  • Rat
  • Reperfusion
  • Substance P

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Cite this

Neuropeptide depletion impairs postischemic recovery of the isolated rat heart : Role of substance p. / Ustinova, Elena E.; Bergren, Dale; Schultz, Harold D.

In: Cardiovascular Research, Vol. 30, No. 1, 01.01.1995, p. 55-63.

Research output: Contribution to journalArticle

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abstract = "Objectives: Ischemia of the myocardium stimulates cardiac sensory nerve endings resulting in the local release of neuropeptides. The significance of the release of neuropeptides, such as substance P (SP), for the function of the heart during ischemia and reperfusion is not known. We examined the effects of both chronic and acute neuropeptide depletion and of SP administration on contractile function and rhythmicity of the isolated rat heart during global ischemia and subsequent reperfusion. Methods: Experiments were conducted on the isolated perfused heart from vehicle and capsaicin-pretreated rats (100 mg/kg) to deplete neuropeptides from peripheral nerve terminals. The hearts were perfused with Krebs-Henseleit solution (95{\%}O2 + 5{\%} CO2, 37 °C, at constant pressure of 90 cmH2O). Left ventricular developed and diastolic pressures (LVDevP and LVEDP), heart rate (HR) and coronary flow (CF) were measured. Hearts were subjected to 20 min global no-flow ischemia and 30 min reperfusion. Results: Prior to interrupting coronary flow, LV pressures, HR and CF did not differ between vehicle and capsaicin-pretreated rats. However, throughout the reperfusion period, the recovery of LVDevP, HR and CF in hearts from capsaicin-pretreated rats was consistently less than in control hearts (P ` 0.05), and the incidence of fibrillation during reperfusion was higher (P ` 0.05). In other experiments, acute perfusion of isolated hearts with capsaicin (10−6 M) for 5 min before ischemia had a similar limiting effect during reperfusion. Administration of SP (10−6–10−9 M) to capsaicin-pretreated hearts before ischemia restored their ability to recover contractile function and CF during reperfusion. Administration of SP to untreated hearts before ischemia also improved their recovery above normal during reperfusion and decreased the incidence of fibrillation without affecting postischemic CF. The beneficial effects of SP were abolished by an NK-1 receptor antagonist, CP-96,345 (10−6 M). Conclusions: These data indicate that sensory neuropeptides play a role in protection of the isolated heart against ischemic damage and suggest a role of SP in the resistance of the myocardium to ischemia and reperfusion injury.",
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N2 - Objectives: Ischemia of the myocardium stimulates cardiac sensory nerve endings resulting in the local release of neuropeptides. The significance of the release of neuropeptides, such as substance P (SP), for the function of the heart during ischemia and reperfusion is not known. We examined the effects of both chronic and acute neuropeptide depletion and of SP administration on contractile function and rhythmicity of the isolated rat heart during global ischemia and subsequent reperfusion. Methods: Experiments were conducted on the isolated perfused heart from vehicle and capsaicin-pretreated rats (100 mg/kg) to deplete neuropeptides from peripheral nerve terminals. The hearts were perfused with Krebs-Henseleit solution (95%O2 + 5% CO2, 37 °C, at constant pressure of 90 cmH2O). Left ventricular developed and diastolic pressures (LVDevP and LVEDP), heart rate (HR) and coronary flow (CF) were measured. Hearts were subjected to 20 min global no-flow ischemia and 30 min reperfusion. Results: Prior to interrupting coronary flow, LV pressures, HR and CF did not differ between vehicle and capsaicin-pretreated rats. However, throughout the reperfusion period, the recovery of LVDevP, HR and CF in hearts from capsaicin-pretreated rats was consistently less than in control hearts (P ` 0.05), and the incidence of fibrillation during reperfusion was higher (P ` 0.05). In other experiments, acute perfusion of isolated hearts with capsaicin (10−6 M) for 5 min before ischemia had a similar limiting effect during reperfusion. Administration of SP (10−6–10−9 M) to capsaicin-pretreated hearts before ischemia restored their ability to recover contractile function and CF during reperfusion. Administration of SP to untreated hearts before ischemia also improved their recovery above normal during reperfusion and decreased the incidence of fibrillation without affecting postischemic CF. The beneficial effects of SP were abolished by an NK-1 receptor antagonist, CP-96,345 (10−6 M). Conclusions: These data indicate that sensory neuropeptides play a role in protection of the isolated heart against ischemic damage and suggest a role of SP in the resistance of the myocardium to ischemia and reperfusion injury.

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