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Blood flow modeling reveals improved collateral artery performance during the regenerative period in mammalian hearts.
Anbazhakan, Suhaas; Rios Coronado, Pamela E; Sy-Quia, Ana Natalia L; Seow, Lek Wei; Hands, Aubrey M; Zhao, Mingming; Dong, Melody L; Pfaller, Martin R; Amir, Zhainib A; Raftrey, Brian C; Cook, Christopher K; D'Amato, Gaetano; Fan, Xiaochen; Williams, Ian M; Jha, Sawan K; Bernstein, Daniel; Nieman, Koen; Pașca, Anca M; Marsden, Alison L; Horse, Kristy Red.
Afiliación
  • Anbazhakan S; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
  • Rios Coronado PE; These authors contributed equally.
  • Sy-Quia ANL; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Seow LW; These authors contributed equally.
  • Hands AM; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Zhao M; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Dong ML; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Pfaller MR; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
  • Amir ZA; Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Raftrey BC; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
  • Cook CK; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
  • D'Amato G; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
  • Fan X; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Williams IM; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Jha SK; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Bernstein D; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Nieman K; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Pașca AM; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Marsden AL; Department of Biology, Stanford University, Stanford, CA 94305, USA.
  • Horse KR; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
Nat Cardiovasc Res ; 1(8): 775-790, 2022 Aug.
Article en En | MEDLINE | ID: mdl-37305211
ABSTRACT
Collateral arteries bridge opposing artery branches, forming a natural bypass that can deliver blood flow downstream of an occlusion. Inducing coronary collateral arteries could treat cardiac ischemia, but more knowledge on their developmental mechanisms and functional capabilities is required. Here we used whole-organ imaging and three-dimensional computational fluid dynamics modeling to define spatial architecture and predict blood flow through collaterals in neonate and adult mouse hearts. Neonate collaterals were more numerous, larger in diameter and more effective at restoring blood flow. Decreased blood flow restoration in adults arose because during postnatal growth coronary arteries expanded by adding branches rather than increasing diameters, altering pressure distributions. In humans, adult hearts with total coronary occlusions averaged 2 large collaterals, with predicted moderate function, while normal fetal hearts showed over 40 collaterals, likely too small to be functionally relevant. Thus, we quantify the functional impact of collateral arteries during heart regeneration and repair-a critical step toward realizing their therapeutic potential.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Nat Cardiovasc Res Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Nat Cardiovasc Res Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos