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Angiotensin II and baroreflex control of heart rate.
Abstract
Angiotensin increases blood pressure without decreasing heart rate because it resets the baroreflex control of heart rate to a higher pressure. The resetting is mediated by central AT1 receptors and withdrawal of cardiac vagal tone. It is physiologically important because it minimizes baroreflex buffering and enhances the peptide's pressor activity.
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In the citing paper
“angiotensin II resets the baroreflex control of heart rate to a higher pressure (Reid, 1996)”
From Thoroughly Calibrated Modular Agent-Based Model of the Human Cardiovascular and Renal Systems for Blood Pressure Regulation in Health and Disease (2021) · cites this paper as Reid, 1996
In the citing paper
“At the same time, the action of angiotensin II in humans is associated either with no change in heart rate or with a reduction that is much smaller than that produced by other vasoconstrictors (Reid, 1996).”
From Thoroughly Calibrated Modular Agent-Based Model of the Human Cardiovascular and Renal Systems for Blood Pressure Regulation in Health and Disease (2021) · cites this paper as Reid, 1996
Citations
Cited by
THE KIDNEY IN BLOOD PRESSURE REGULATION AND DEVELOPMENT OF HYPERTENSION
Navar, L. G. (1997) · Medical Clinics of North America · doi:10.1016/s0025-7125(05)70573-3 · Cited by 85
Tan, P. S. P., Killinger, S., Horiuchi, J., et al. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00267.2007 · Cited by 60
Relationships Between Blood Pressure and Heart Rate in the Saltwater Crocodile Crocodylus Porosus
Altimiras, J., Franklin, C. E., & Axelsson, M. (1998) · Journal of Experimental Biology · doi:10.1242/jeb.201.15.2235 · Cited by 53
Hagensen, M. K., Abe, A. S., & Wang, T. (2010) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2010.03.028 · Cited by 31
Mass Transport: Circulatory System with Emphasis on Nonendothermic Species
Crossley, D. A., Burggren, W. W., Reiber, C. L., Altimiras, J., & Rodnick, K. J. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150010 · Cited by 27
Temperature effects on baroreflex control of heart rate in the toad, Rhinella schneideri
Zena, L. A., Gargaglioni, L. H., & Bícego, K. C. (2014) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2014.09.027 · Cited by 21
“Using GraphPad Prism, MAP (kPa) plotted against HR (bpm) data were fitted to a four-variable sigmoidal logistic function as described previously (Reid, 1996):”
MethodANG II and baroreflex control of heart rate in embryonic chickens (Gallus gallus domesticus)
Mueller, C. A., Burggren, W. W., & Crossley, D. A. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00298.2013 · Cited by 21
Martínez, N. I., Panciera, D. L., Abbott, J. A., & Ward, D. L. (2004) · Research in Veterinary Science · doi:10.1016/j.rvsc.2004.05.004 · Cited by 20
“It increases blood pressure without decreasing heart rate because it resets the baroreceptor reflex control of heart rate to a higher pressure.(31) Brain angiotensin II could be involved in the regulation of cardiac reflexes since cerebrospinal fluid angiotensin II concentration remained unchanged despite undetectable…”
BackgroundZena, L. A., Dantonio, V., Gargaglioni, L. H., et al. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.129130 · Cited by 18
“The relationship between PMA and fH for each tegu was analyzed using a four-variable sigmoidal logistic function as described previously by Reid (1996): fH ¼ ðA DÞ 1þ ðPMA=CÞB þ D; ð1Þ where A is the maximum fH (beats min −1), D is the minimum fH of the curve, B is the slope coefficient (beats…”
MethodKutumova, E., Kiselev, I., Sharipov, R., Lifshits, G., & Kolpakov, F. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.746300 · Cited by 16
“Such a decision was based on the facts that angiotensin II resets the baroreflex control of heart rate to a higher pressure (Reid, 1996) and increases the release of norepinephrine from the atria (Brasch et al., 1993).”
BackgroundBaroreflex function in anurans from different environments
Hedrick, M. S., McNew, K. A., & Crossley, D. A. (2014) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2014.10.001 · Cited by 17
Monument, M. J., & Smith, F. G. (2003) · Experimental Physiology · doi:10.1113/eph8802602 · Cited by 15
“For example, ANG II resets the arterial baroreflex control of HR towards higher pressures in conscious animals (Reid & Chou, 1990; Brooks et al. 1993; Wong et al. 1993; Reid, 1996).”
BackgroundEvaluation of the sequence method as a tool to assess spontaneous baroreflex in reptiles
Filogonio, R., Orsolini, K. F., Castro, S. A., et al. (2019) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2273 · Cited by 14
Baroreflex regulation affects ventilation in the cururu toad R hinella schneideri
Zena, L. A., da Silva, G. S. F., Gargaglioni, L. H., & Bícego, K. C. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.144774 · Cited by 14
“…against PMA (kPa) data obtained for each animal at each temperature and fitted to a four-variable sigmoidal logistic function as described previously by Reid (1996): fH ¼ ðA DÞ 1þ ðPMA=CÞB þ D; ð1Þ where A is maximum fH and D is minimum fH (beats min −1) of the curve, B is the slope coefficient…”
Crossley, D. A., Wearing, O. H., Platzack, B., et al. (2015) · Journal of Comparative Physiology B · doi:10.1007/s00360-015-0896-6 · Cited by 11
“The corresponding Pm and ƒH were analyzed for each animal using a four-variable sigmoidal logistic function (Altimiras et al. 1998; Reid 1996): where, max and min are the maximum and minimum ƒH (min−1), respectively, attained across the pressure range; B is the maximum slope of the linear portion…”
MethodArmelin, V. A., Braga, V. H. D. S., Teixeira, M. T., et al. (2021) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2021.110916 · Cited by 11
Armelin, V. A., Thomsen, M. T., Teixeira, M. T., Florindo, L. H., Bayley, M., & Wang, T. (2019) · Journal of Comparative Physiology B · doi:10.1007/s00360-019-01225-9 · Cited by 10
Armelin, V. A., Braga, V. H. D. S., Teixeira, M. T., et al. (2021) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2448 · Cited by 10
Hwang, K. Y., Phoon, P. H. Y., & Hwang, N. C. (2023) · Journal of Cardiothoracic and Vascular Anesthesia · doi:10.1053/j.jvca.2023.12.016 · Cited by 11
Baroreflex responses of decerebrate rattlesnakes (Crotalus durissus) are comparable to awake animals
Tavares, D., Matos, S. L. B. D. S., Duran, L. M., Castro, S. A., Taylor, E. W., Filogonio, R., Fernandes, M. N., & Leite, C. A. C. (2022) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2022.111286 · Cited by 10
Nelson, D., Crossley, D. A., Elsey, R. M., et al. (2018) · Journal of Comparative Physiology B · doi:10.1007/s00360-018-1144-7 · Cited by 6
Cardiovascular contributions and energetic costs of thermoregulation in ectothermic vertebrates
Parlin, A. F., & Schaeffer, P. J. (2022) · Journal of Experimental Biology · doi:10.1242/jeb.243095 · Cited by 6
Mueller, C. A., Eme, J., Tate, K. B., et al. (2018) · Journal of Comparative Physiology B · doi:10.1007/s00360-018-1157-2 · Cited by 6
El-Etriby, A. M. K., & Rakha, S. (2020) · Current Medical Research and Opinion · doi:10.1080/03007995.2020.1719394 · Cited by 4
A comparison of four common mathematical models to assess baroreflex sensitivity
Filogonio, R., & Leite, C. A. C. (2023) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2708 · Cited by 4
Slivkoff, M. D., & Warburton, S. J. (2003) · General and Comparative Endocrinology · doi:10.1016/s0016-6480(03)00058-3 · Cited by 3
The vasopressor action of angiotensin II (ANG II) in ball pythons (Python regius)
Hansen, L. M. B., & Wang, T. (2020) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2020.110839 · Cited by 2
Reprint of “Baroreflex function in anurans from different environments”
Hedrick, M. S., McNew, K. A., & Crossley, D. A. (2015) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2015.03.016 · Cited by 1
“Because changes in fH and blood pressure reach lower and upper limits at either end of the range (i.e. threshold and saturation, respectively), there is a sigmoidal, rather than linear, relationship between fH and Pm (Kent et al., 1972; Reid, 1996).”
BackgroundMethodInfluential
Metadata
- Authors
- Reid, I.
- Corresponding author
- Reid, IA
- Venue
- Physiology
- Publisher
- American Physiological Society
- Published
- 1996-12-01
- Volume
- 11
- Issue
- 6
- Pages
- 270-274
- ISSN
- 0886-1714 (ISSN-L)
- 1548-9213
- 1548-9221
- OpenAlex
- W2255753006
- Cited by
- 30
- References
- 0
- Citations by year
- 2023: 2 · 2022: 2 · 2021: 3 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 2 · 2014: 2 · 2013: 1
- FWCI
- 0.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Physiology (publishedVersion)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Rate Variability and Autonomic Control
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Health Sciences › Medicine › Surgery › Cardiovascular, Neuropeptides, and Oxidative Stress Research
- Keywords
- angiotensin II, baroreflex, heart rate, baroreflex resetting, angiotensin II type 1 receptor, cardiac vagal tone, blood pressure, pressor activity
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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