TY - JOUR
T1 - The impact of theaflavins on systemic-and microcirculation alterations
T2 - The murine and randomized feasibility trials
AU - Saito, Akiko
AU - Nakazato, Risa
AU - Suhara, Yoshitomo
AU - Shibata, Masahiro
AU - Fukui, Toshiki
AU - Ishii, Takeshi
AU - Asanuma, Toshimichi
AU - Mochizuki, Kazuo
AU - Nakayama, Tsutomu
AU - Osakabe, Naomi
N1 - Funding Information:
Supporting Information: This work was supported by a Grant-in-Aid for Scientific Research from the Japan Science and Technology Agency (JST) under the Broader Collaboration of Regional Entities for the Advancement of Technological Excellence (CREATE) Program, the Research Project on Development of Agricultural Products and Foods with Health-promoting Benefits from the National Agriculture and Food Research Organization (NARO) and the Grant of Cross-Ministerial Strategic Innovation Promotion Program (SIP), Urgent Project for Development and Diffusion of Innovative Technology towards Realization of the Aggressive Agriculture, Forestry, and Fisheries, Japan. CREAT:http://www.shizuoka-tiikikesshu.jp/outline/index.html SIP:http://www8.cao.go.jp/cstp/gaiyo/sip/ NARO:http://www.naro.affrc.go.jp/project/f_foodpro/index.html.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Theaflavins are polyphenols found in black tea; their physiological activities were not well investigated. The present study in rats evaluated the influence of theaflavins on circulation. In addition, an intervention pilot study examined the influence of a theaflavin drink on postprandial hemodynamic change. In an animal study, a single oral dose of theaflavin rich fraction (TF, 10 mg/kg) caused transient increase in mean blood pressure (MBP) and heart rate (HR). TF also elevated cremastric blood flow significantly, and the magnitude of this effect was in this order: theaflavin 3'-O-gallate (TF2B) > > theaflavin-3-O-gallate (TF2A) > > theaflavin (TF1) = theaflavin-3, 3'-di-O-gallate (TF3). In addition, these hemodynamic alterations in mammals totally disappeared when pretreated with carvedilol as an adrenaline blocker. We also treated 10-mg/kg/day TF to the rats for 2 weeks. At the end of the ingestion period, MBP was reduced significantly, and aortic eNOS level was elevated by the repeated ingestion of TF compared with distilled water. In the intervention trial, blood pressure of the volunteers was increased significantly 2 and 4 h after ingestion of the TF drink (45 mg/drink) compared with before treatment. A significant difference was observed in FMD between the placebo and theaflavin groups 4 h after ingestion. These results suggested that theaflavin has potent activity to alter hemodynamics in both murine and healthy subjects. Further studies is needed to elucidate the details; however, the results of animal study suggested that the possible involvement of sympathetic nervous system in the hemodynamic changes caused by TF.
AB - Theaflavins are polyphenols found in black tea; their physiological activities were not well investigated. The present study in rats evaluated the influence of theaflavins on circulation. In addition, an intervention pilot study examined the influence of a theaflavin drink on postprandial hemodynamic change. In an animal study, a single oral dose of theaflavin rich fraction (TF, 10 mg/kg) caused transient increase in mean blood pressure (MBP) and heart rate (HR). TF also elevated cremastric blood flow significantly, and the magnitude of this effect was in this order: theaflavin 3'-O-gallate (TF2B) > > theaflavin-3-O-gallate (TF2A) > > theaflavin (TF1) = theaflavin-3, 3'-di-O-gallate (TF3). In addition, these hemodynamic alterations in mammals totally disappeared when pretreated with carvedilol as an adrenaline blocker. We also treated 10-mg/kg/day TF to the rats for 2 weeks. At the end of the ingestion period, MBP was reduced significantly, and aortic eNOS level was elevated by the repeated ingestion of TF compared with distilled water. In the intervention trial, blood pressure of the volunteers was increased significantly 2 and 4 h after ingestion of the TF drink (45 mg/drink) compared with before treatment. A significant difference was observed in FMD between the placebo and theaflavin groups 4 h after ingestion. These results suggested that theaflavin has potent activity to alter hemodynamics in both murine and healthy subjects. Further studies is needed to elucidate the details; however, the results of animal study suggested that the possible involvement of sympathetic nervous system in the hemodynamic changes caused by TF.
KW - Adrenalin receptor blocker
KW - Circulation
KW - FMD
KW - Theaflavin
KW - eNOS
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U2 - 10.1016/j.jnutbio.2016.01.012
DO - 10.1016/j.jnutbio.2016.01.012
M3 - Article
C2 - 27142743
AN - SCOPUS:84962646556
SN - 0955-2863
VL - 32
SP - 107
EP - 114
JO - Journal of Nutritional Biochemistry
JF - Journal of Nutritional Biochemistry
ER -