Your browser doesn't support javascript.
loading
Conjugated bile acids are nutritionally re-programmable antihypertensive metabolites.
Chakraborty, Saroj; Lulla, Anju; Cheng, Xi; Yeo, Ji-Youn; Mandal, Juthika; Yang, Tao; Mei, Xue; Saha, Piu; Golonka, Rachel M; Yeoh, Beng San; Mell, Blair; Jia, Wei; Putluri, Vasanta; Piyarathna, Danthasinghe Waduge Badrajee; Putluri, Nagireddy; Sreekumar, Arun; Meyer, Katie; Vijay-Kumar, Matam; Joe, Bina.
Afiliação
  • Chakraborty S; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Lulla A; Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina.
  • Cheng X; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Yeo JY; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Mandal J; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Yang T; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Mei X; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Saha P; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Golonka RM; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Yeoh BS; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Mell B; Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.
  • Jia W; University of Hawaii Cancer Center, Honolulu, Hawaii.
  • Putluri V; Dan L. Duncan Cancer Center, Advanced Technology Core.
  • Piyarathna DWB; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
  • Putluri N; Dan L. Duncan Cancer Center, Advanced Technology Core.
  • Sreekumar A; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
  • Meyer K; Dan L. Duncan Cancer Center, Advanced Technology Core.
  • Vijay-Kumar M; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
  • Joe B; Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina.
J Hypertens ; 41(6): 979-994, 2023 06 01.
Article em En | MEDLINE | ID: mdl-37071431
ABSTRACT

BACKGROUND:

Hypertension is the largest risk factor affecting global mortality. Despite available medications, uncontrolled hypertension is on the rise, whereby there is an urgent need to develop novel and sustainable therapeutics. Because gut microbiota is now recognized as an important entity in blood pressure regulation, one such new avenue is to target the gut-liver axis wherein metabolites are transacted via host-microbiota interactions. Knowledge on which metabolites within the gut-liver axis regulate blood pressure is largely unknown.

METHOD:

To address this, we analyzed bile acid profiles of human, hypertensive and germ-free rat models and report that conjugated bile acids are inversely correlated with blood pressure in humans and rats.

RESULTS:

Notably intervening with taurine or tauro-cholic acid rescued bile acid conjugation and reduced blood pressure in hypertensive rats. Subsequently, untargeted metabolomics uncovered altered energy metabolism following conjugation of bile acids as a mechanism alleviating high blood pressure.

CONCLUSION:

Together this work reveals conjugated bile acids as nutritionally re-programmable anti-hypertensive metabolites.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertensão / Anti-Hipertensivos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Hypertens Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertensão / Anti-Hipertensivos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Hypertens Ano de publicação: 2023 Tipo de documento: Article