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BPC-157 is stable in gastric acid (unlike most peptides), which is one of its distinguishing pharmacologic properties 1

In addition, SS-31-treated cells exhibited increased eNOS expression, supporting a direct role of mitochondrial protection in improving nitric oxide bioavailability [49]

Based on the recent Fourier transform infrared (FTIR) spectroscopy vascular disturbance studies, particularly those after unilateral adrenalectomy in rats, the noted cytoprotective vascular recovery effect of the BPC 157 therapy may be useful