Key result
GAXGLXGP stimulates endothelial nitric oxide production by phosphorylating eNOS at Ser1179.
Why the study?
Does the octapeptide GAXGLXGP stimulate nitric oxide synthesis in vascular endothelial cells?
Does the octapeptide GAXGLXGP stimulate nitric oxide synthesis in vascular endothelial cells?
The octapeptide GAXGLXGP can be absorbed intact through intestinal epithelium and directly stimulates eNOS activity and NO synthesis in vascular endothelial cells, suggesting potential for improving vascular function.
Answers are grounded in this paper and cite their sources.
May support vascular peptide research; leaves open any endothelial benefit in humans pending clinical trials.
Gly-Ala-Hyp-Gly-Leu-Hyp-Gly-Pro (GAXGLXGP, X: Hyp), an octapeptide contained in chicken collagen hydrolysate, inhibits angiotensin I-converting enzyme activity in vitro. Intestinal Caco-2 and bovine aortic endothelial cells (BAECs) were used to investigate whether the transported GAXGLXGP improves vascular function. When GAXGLXGP was added to the apical side of Caco-2 monolayers, the intact form of GAXGLXGP was released to the basolateral side without incorporation into the cells. This transport was energy-independent but was associated with tight junction permeability. GAXGLXGP was then added to BAECs, and endothelial nitric oxide (NO) synthase (eNOS) activation was examined. GAXGLXGP at a concentration of 10 microM stimulated production of NO during a 1 h incubation. This event involved phosphorylation of eNOS at Ser(1179) without a change in the total eNOS protein level. These findings indicate that GAXGLXGP absorbed intact through the intestinal epithelium has direct effects on eNOS activity in vascular endothelial cells, leading to NO synthesis, thereby suggesting the potential for improvement in vascular function.
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Shimizu et al. (2010) studied this question. Gly-Ala-Hyp-Gly-Leu-Hyp-Gly-Pro (GAXGLXGP) was evaluated on Nitric oxide (NO) production and eNOS activation. GAXGLXGP at 10 microM stimulated production of nitric oxide in bovine aortic endothelial cells during a 1-hour incubation by phosphorylating eNOS at Ser(1179).
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