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Influence of angiotensin II and telmisartan on in vivo high-resolution renal arterial impedance in rats.
Fukuda, Yukiko; Kawada, Toru; Kataoka, Yasuyuki; Peterson, Jon; Saku, Keita; Alexander, Joe; Sunagawa, Kenji.
Afiliación
  • Fukuda Y; Medical and Health Informatics Laboratories, NTT Research, Inc., Sunnyvale, California, United States.
  • Kawada T; Department of Cardiovascular Dynamics, National Cerebral and Cardiovascular Center, Osaka, Japan.
  • Kataoka Y; Medical and Health Informatics Laboratories, NTT Research, Inc., Sunnyvale, California, United States.
  • Peterson J; Medical and Health Informatics Laboratories, NTT Research, Inc., Sunnyvale, California, United States.
  • Saku K; Department of Cardiovascular Dynamics, National Cerebral and Cardiovascular Center, Osaka, Japan.
  • Alexander J; Bio Digital Twin Center, National Cerebral and Cardiovascular Center, Osaka, Japan.
  • Sunagawa K; Medical and Health Informatics Laboratories, NTT Research, Inc., Sunnyvale, California, United States.
Am J Physiol Regul Integr Comp Physiol ; 327(3): R349-R361, 2024 Sep 01.
Article en En | MEDLINE | ID: mdl-39005079
ABSTRACT
Angiotensin II (ANG II) is known to play an important role in regulating renal hemodynamics. We sought to quantify this effect in an in vivo rat model with high-resolution renal arterial (RA) impedance. This study examines the effects of ANG II and its type 1 receptor blocker telmisartan (TELM) on RA impedance. In baroreflex-deactivated rats, we measured RA pressure (Pr) and blood flow (Fr) during random ventricular pacing to induce pressure fluctuation at three different mean Pr (60, 80, and 100 mmHg). We then estimated RA impedance as the transfer function from Fr to Pr. The RA impedance was found to align with a three-element Windkessel model consisting of proximal (Rp) and distal (Rd) resistance and compliance (C). Our study showed Rd reflected the composite characteristics of afferent and efferent arterioles. Rd increased with increasing Pr under the baseline condition with a slope of 1.03 ± 0.21 (× 10-1) min·mL-1. ANG II significantly increased the slope by 0.72 ± 0.29 (× 10-1) min·mL-1 (P < 0.05) without affecting the intercept. TELM significantly reduced the intercept by 34.49 ± 4.86 (× 10-1) mmHg·min·mL-1 (P < 0.001) from the baseline value of 37.93 ± 13.36 (× 10-1) mmHg·min·mL-1, whereas it did not affect the slope. In contrast, Rp was less sensitive than Rd to ANG II or TELM, suggesting Rp may represent the characteristics of elastic large arteries. Our findings provide valuable insights into the influence of ANG II on the dynamics of the renal vasculature.NEW & NOTEWORTHY This present method of quantifying high-resolution renal arterial impedance could contribute to elucidating the characteristics of renal vasculature influenced by physiological mechanisms, renal diseases, or pharmacological effects. The present findings help construct a lumped-parameter renal hemodynamic model that reflects the influence of angiotensin II.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Arteria Renal / Circulación Renal / Resistencia Vascular / Angiotensina II / Ratas Sprague-Dawley / Bloqueadores del Receptor Tipo 1 de Angiotensina II / Telmisartán Límite: Animals Idioma: En Revista: Am J Physiol Regul Integr Comp Physiol Asunto de la revista: FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Arteria Renal / Circulación Renal / Resistencia Vascular / Angiotensina II / Ratas Sprague-Dawley / Bloqueadores del Receptor Tipo 1 de Angiotensina II / Telmisartán Límite: Animals Idioma: En Revista: Am J Physiol Regul Integr Comp Physiol Asunto de la revista: FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos