TY - JOUR
T1 - Additive beneficial effects of lactotripeptides and aerobic exercise on arterial compliance in postmenopausal women
AU - Yoshizawa, Mutsuko
AU - Maeda, Seiji
AU - Miyaki, Asako
AU - Misono, Maiko
AU - Choi, Youngju
AU - Shimojo, Nobutake
AU - Ajisaka, Ryuichi
AU - Tanaka, Hirofumi
PY - 2009/11
Y1 - 2009/11
N2 - Central arterial compliance plays an important role in the functional abilities of the vasculature. Two active tripeptides, valine-proline-proline and isoleucine-proline-proline, were isolated from sour milk and were referred to as lactotripeptides (LTP). Because LTP appears to act as an angiotensin- converting enzyme inhibitor, it is plausible to hypothesize that LTP improves arterial compliance. We determined the effects of LTP ingestion alone or in combination with regular aerobic exercise on arterial compliance. A total of 55 postmenopausal women (50-65 yr old) were randomly divided into four groups: placebo, LTP, exercise and placebo (Ex + placebo), or exercise and LTP (Ex + LTP). LTP or placebo was administered orally for 8 wk. The exercise groups completed an 8-wk moderate aerobic exercise intervention. There were no differences in baseline arterial compliance and most other key dependent variables among the groups. Carotid arterial compliance increased significantly in the LTP (0.93 ± 0.07 vs. 0.99 ± 0.08 mm2/ mmHg·10-1), Ex + placebo (0.92 ± 0.04 vs. 1.00 ± 0.05 mm2/mmHg·10-1), and Ex + LTP groups (0.86 ± 0.06 vs. 1.00 ± 0.06 mm2/mmHg·10 -1), whereas no such changes were observed in the placebo control group (0.86 ± 0.06 vs. 0.85 ± 0.07 mm2/ mmHg·10-1). The magnitude of increases in carotid arterial compliance was significantly greater in the Ex + LTP group (19 ± 4%) than in other groups. The improvements in arterial compliance with LTP were associated with the corresponding reductions in arterial blood pressure and plasma angiotensin II concentrations. We concluded that LTP ingestion improves carotid arterial compliance and that the combination of LTP ingestion and regular exercise is additive and synergistic in improving arterial compliance in postmenopausal women.
AB - Central arterial compliance plays an important role in the functional abilities of the vasculature. Two active tripeptides, valine-proline-proline and isoleucine-proline-proline, were isolated from sour milk and were referred to as lactotripeptides (LTP). Because LTP appears to act as an angiotensin- converting enzyme inhibitor, it is plausible to hypothesize that LTP improves arterial compliance. We determined the effects of LTP ingestion alone or in combination with regular aerobic exercise on arterial compliance. A total of 55 postmenopausal women (50-65 yr old) were randomly divided into four groups: placebo, LTP, exercise and placebo (Ex + placebo), or exercise and LTP (Ex + LTP). LTP or placebo was administered orally for 8 wk. The exercise groups completed an 8-wk moderate aerobic exercise intervention. There were no differences in baseline arterial compliance and most other key dependent variables among the groups. Carotid arterial compliance increased significantly in the LTP (0.93 ± 0.07 vs. 0.99 ± 0.08 mm2/ mmHg·10-1), Ex + placebo (0.92 ± 0.04 vs. 1.00 ± 0.05 mm2/mmHg·10-1), and Ex + LTP groups (0.86 ± 0.06 vs. 1.00 ± 0.06 mm2/mmHg·10 -1), whereas no such changes were observed in the placebo control group (0.86 ± 0.06 vs. 0.85 ± 0.07 mm2/ mmHg·10-1). The magnitude of increases in carotid arterial compliance was significantly greater in the Ex + LTP group (19 ± 4%) than in other groups. The improvements in arterial compliance with LTP were associated with the corresponding reductions in arterial blood pressure and plasma angiotensin II concentrations. We concluded that LTP ingestion improves carotid arterial compliance and that the combination of LTP ingestion and regular exercise is additive and synergistic in improving arterial compliance in postmenopausal women.
KW - Arterial stiffness
KW - Fermented milk
KW - Lifestyle
KW - Peptide
KW - Physical activity
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U2 - 10.1152/ajpheart.00433.2009
DO - 10.1152/ajpheart.00433.2009
M3 - Article
C2 - 19783777
AN - SCOPUS:70350448855
SN - 0363-6135
VL - 297
SP - H1899-H1903
JO - American Journal of Physiology - Heart and Circulatory Physiology
JF - American Journal of Physiology - Heart and Circulatory Physiology
IS - 5
ER -