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Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inh...
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| Zeitschriftentitel: | Journal of Autonomic Pharmacology |
|---|---|
| Personen und Körperschaften: | , , , , , , |
| In: | Journal of Autonomic Pharmacology, 18, 1998, 5, S. 271-280 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
|
| Schlagwörter: |
| author_facet |
Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. |
|---|---|
| author |
Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. |
| spellingShingle |
Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. Journal of Autonomic Pharmacology Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors Pharmacology General Neuroscience |
| author_sort |
bernardi, m. |
| spelling |
Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. 0144-1795 1365-2680 Wiley Pharmacology General Neuroscience http://dx.doi.org/10.1046/j.1365-2680.1998.18593.x <jats:p> <jats:bold>1</jats:bold> Frequency‐domain spectral analysis of stationary ECG R‐R intervals was made by fast Fourier transformation (FFT) in conditions of monitored arterial blood pressure and respiratory activity in diethyl‐ether‐anaesthetized and pithed adult rats. This technique yields a number of parameters which allow quantitative evaluation of the non‐random distribution of the mean values obtained in time‐domain studies. The frequency‐analysis method enables the overall heart rate variability to be broken down into its various constituents, which are differently affected by physiological loading and capable of selective reactivity to pharmacological agents.</jats:p><jats:p> <jats:bold>2</jats:bold> The low‐frequency spectral component obtained by breaking down the total spectral density power, i.e. the appropriate variability signal (band width < 0.15 Hz) and a higher‐frequency band corresponding to spontaneous (0.80–1.60 Hz) or artificially imposed (0.75 Hz) respiratory activity were estimated and their integrated areas evaluated as absolute powers or normalized fractional values.</jats:p><jats:p> <jats:bold>3</jats:bold> The power of the high‐frequency spectral component increased in all animal preparations under treatment with prazosin, <jats:italic>dl</jats:italic>‐propranolol, endothelin‐1 and the angiotensin converting enzyme (ACE) inhibitors captopril, lisinopril, quinapril and ramipril. The power of the low‐frequency band increased under α‐r atriopeptin and ACE inhibitors in the pithed preparations only, and decreased in the anaesthetized animals.</jats:p><jats:p> <jats:bold>4</jats:bold> The new power spectrum features and trends detected indicate that these time‐independent, model‐dependent cardiovascular and respiratory markers are subject to some form of complex peptidergic control.</jats:p><jats:p> <jats:bold>5</jats:bold> The relative roles of the various factors operating in the genesis of these short‐term changes in spectral power in the low‐ and high‐frequency bands cannot be interpreted as indicating a reciprocal push–pull relationship between sympathetic and parasympathetic control.</jats:p><jats:p> <jats:bold>6</jats:bold> The study findings, however, can be interpreted as providing evidence of a different and to some extent alternative form of integrative cardiovascular control persisting in the pithed rats (i.e. in the ‘peripheral’, CNS‐destroyed preparations).</jats:p><jats:p> <jats:bold>7</jats:bold> New areas of theoretical and applied research are being developed in the (auto)classification of (iso)receptors and drug analogues through exploration of multiple physiological and pharmacokinetic parameters in the frequency‐domain. Furthermore, model‐independent frequency‐domain methods not requiring stationary data will afford scope for even more significant developments by separating the overlapping dynamic processes from a whole series of correlated effects.</jats:p> Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors Journal of Autonomic Pharmacology |
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1998 |
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Journal of Autonomic Pharmacology |
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49 |
| title |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_unstemmed |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_full |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_fullStr |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_full_unstemmed |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_short |
Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_sort |
spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ace‐inhibitors |
| topic |
Pharmacology General Neuroscience |
| url |
http://dx.doi.org/10.1046/j.1365-2680.1998.18593.x |
| publishDate |
1998 |
| physical |
271-280 |
| description |
<jats:p> <jats:bold>1</jats:bold> Frequency‐domain spectral analysis of stationary ECG R‐R intervals was made by fast Fourier transformation (FFT) in conditions of monitored arterial blood pressure and respiratory activity in diethyl‐ether‐anaesthetized and pithed adult rats. This technique yields a number of parameters which allow quantitative evaluation of the non‐random distribution of the mean values obtained in time‐domain studies. The frequency‐analysis method enables the overall heart rate variability to be broken down into its various constituents, which are differently affected by physiological loading and capable of selective reactivity to pharmacological agents.</jats:p><jats:p> <jats:bold>2</jats:bold> The low‐frequency spectral component obtained by breaking down the total spectral density power, i.e. the appropriate variability signal (band width < 0.15 Hz) and a higher‐frequency band corresponding to spontaneous (0.80–1.60 Hz) or artificially imposed (0.75 Hz) respiratory activity were estimated and their integrated areas evaluated as absolute powers or normalized fractional values.</jats:p><jats:p> <jats:bold>3</jats:bold> The power of the high‐frequency spectral component increased in all animal preparations under treatment with prazosin, <jats:italic>dl</jats:italic>‐propranolol, endothelin‐1 and the angiotensin converting enzyme (ACE) inhibitors captopril, lisinopril, quinapril and ramipril. The power of the low‐frequency band increased under α‐r atriopeptin and ACE inhibitors in the pithed preparations only, and decreased in the anaesthetized animals.</jats:p><jats:p> <jats:bold>4</jats:bold> The new power spectrum features and trends detected indicate that these time‐independent, model‐dependent cardiovascular and respiratory markers are subject to some form of complex peptidergic control.</jats:p><jats:p> <jats:bold>5</jats:bold> The relative roles of the various factors operating in the genesis of these short‐term changes in spectral power in the low‐ and high‐frequency bands cannot be interpreted as indicating a reciprocal push–pull relationship between sympathetic and parasympathetic control.</jats:p><jats:p> <jats:bold>6</jats:bold> The study findings, however, can be interpreted as providing evidence of a different and to some extent alternative form of integrative cardiovascular control persisting in the pithed rats (i.e. in the ‘peripheral’, CNS‐destroyed preparations).</jats:p><jats:p> <jats:bold>7</jats:bold> New areas of theoretical and applied research are being developed in the (auto)classification of (iso)receptors and drug analogues through exploration of multiple physiological and pharmacokinetic parameters in the frequency‐domain. Furthermore, model‐independent frequency‐domain methods not requiring stationary data will afford scope for even more significant developments by separating the overlapping dynamic processes from a whole series of correlated effects.</jats:p> |
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| description | <jats:p> <jats:bold>1</jats:bold> Frequency‐domain spectral analysis of stationary ECG R‐R intervals was made by fast Fourier transformation (FFT) in conditions of monitored arterial blood pressure and respiratory activity in diethyl‐ether‐anaesthetized and pithed adult rats. This technique yields a number of parameters which allow quantitative evaluation of the non‐random distribution of the mean values obtained in time‐domain studies. The frequency‐analysis method enables the overall heart rate variability to be broken down into its various constituents, which are differently affected by physiological loading and capable of selective reactivity to pharmacological agents.</jats:p><jats:p> <jats:bold>2</jats:bold> The low‐frequency spectral component obtained by breaking down the total spectral density power, i.e. the appropriate variability signal (band width < 0.15 Hz) and a higher‐frequency band corresponding to spontaneous (0.80–1.60 Hz) or artificially imposed (0.75 Hz) respiratory activity were estimated and their integrated areas evaluated as absolute powers or normalized fractional values.</jats:p><jats:p> <jats:bold>3</jats:bold> The power of the high‐frequency spectral component increased in all animal preparations under treatment with prazosin, <jats:italic>dl</jats:italic>‐propranolol, endothelin‐1 and the angiotensin converting enzyme (ACE) inhibitors captopril, lisinopril, quinapril and ramipril. The power of the low‐frequency band increased under α‐r atriopeptin and ACE inhibitors in the pithed preparations only, and decreased in the anaesthetized animals.</jats:p><jats:p> <jats:bold>4</jats:bold> The new power spectrum features and trends detected indicate that these time‐independent, model‐dependent cardiovascular and respiratory markers are subject to some form of complex peptidergic control.</jats:p><jats:p> <jats:bold>5</jats:bold> The relative roles of the various factors operating in the genesis of these short‐term changes in spectral power in the low‐ and high‐frequency bands cannot be interpreted as indicating a reciprocal push–pull relationship between sympathetic and parasympathetic control.</jats:p><jats:p> <jats:bold>6</jats:bold> The study findings, however, can be interpreted as providing evidence of a different and to some extent alternative form of integrative cardiovascular control persisting in the pithed rats (i.e. in the ‘peripheral’, CNS‐destroyed preparations).</jats:p><jats:p> <jats:bold>7</jats:bold> New areas of theoretical and applied research are being developed in the (auto)classification of (iso)receptors and drug analogues through exploration of multiple physiological and pharmacokinetic parameters in the frequency‐domain. Furthermore, model‐independent frequency‐domain methods not requiring stationary data will afford scope for even more significant developments by separating the overlapping dynamic processes from a whole series of correlated effects.</jats:p> |
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| spelling | Bernardi, M. Deslauriers, R. Docherty, J. Rossi, C. Rossini, L. Rossini, P. Tonnini, C. 0144-1795 1365-2680 Wiley Pharmacology General Neuroscience http://dx.doi.org/10.1046/j.1365-2680.1998.18593.x <jats:p> <jats:bold>1</jats:bold> Frequency‐domain spectral analysis of stationary ECG R‐R intervals was made by fast Fourier transformation (FFT) in conditions of monitored arterial blood pressure and respiratory activity in diethyl‐ether‐anaesthetized and pithed adult rats. This technique yields a number of parameters which allow quantitative evaluation of the non‐random distribution of the mean values obtained in time‐domain studies. The frequency‐analysis method enables the overall heart rate variability to be broken down into its various constituents, which are differently affected by physiological loading and capable of selective reactivity to pharmacological agents.</jats:p><jats:p> <jats:bold>2</jats:bold> The low‐frequency spectral component obtained by breaking down the total spectral density power, i.e. the appropriate variability signal (band width < 0.15 Hz) and a higher‐frequency band corresponding to spontaneous (0.80–1.60 Hz) or artificially imposed (0.75 Hz) respiratory activity were estimated and their integrated areas evaluated as absolute powers or normalized fractional values.</jats:p><jats:p> <jats:bold>3</jats:bold> The power of the high‐frequency spectral component increased in all animal preparations under treatment with prazosin, <jats:italic>dl</jats:italic>‐propranolol, endothelin‐1 and the angiotensin converting enzyme (ACE) inhibitors captopril, lisinopril, quinapril and ramipril. The power of the low‐frequency band increased under α‐r atriopeptin and ACE inhibitors in the pithed preparations only, and decreased in the anaesthetized animals.</jats:p><jats:p> <jats:bold>4</jats:bold> The new power spectrum features and trends detected indicate that these time‐independent, model‐dependent cardiovascular and respiratory markers are subject to some form of complex peptidergic control.</jats:p><jats:p> <jats:bold>5</jats:bold> The relative roles of the various factors operating in the genesis of these short‐term changes in spectral power in the low‐ and high‐frequency bands cannot be interpreted as indicating a reciprocal push–pull relationship between sympathetic and parasympathetic control.</jats:p><jats:p> <jats:bold>6</jats:bold> The study findings, however, can be interpreted as providing evidence of a different and to some extent alternative form of integrative cardiovascular control persisting in the pithed rats (i.e. in the ‘peripheral’, CNS‐destroyed preparations).</jats:p><jats:p> <jats:bold>7</jats:bold> New areas of theoretical and applied research are being developed in the (auto)classification of (iso)receptors and drug analogues through exploration of multiple physiological and pharmacokinetic parameters in the frequency‐domain. Furthermore, model‐independent frequency‐domain methods not requiring stationary data will afford scope for even more significant developments by separating the overlapping dynamic processes from a whole series of correlated effects.</jats:p> Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors Journal of Autonomic Pharmacology |
| spellingShingle | Bernardi, M., Deslauriers, R., Docherty, J., Rossi, C., Rossini, L., Rossini, P., Tonnini, C., Journal of Autonomic Pharmacology, Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors, Pharmacology, General Neuroscience |
| title | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_full | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_fullStr | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_full_unstemmed | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_short | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| title_sort | spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ace‐inhibitors |
| title_unstemmed | Spectral analysis of intercycle heart fluctuations in the diethyl‐ether‐anaesthetized or pithed rat treated with prazosin, dl‐propranolol, endothelin‐1, α‐r atriopeptin and ACE‐inhibitors |
| topic | Pharmacology, General Neuroscience |
| url | http://dx.doi.org/10.1046/j.1365-2680.1998.18593.x |