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At 42 hours after conditioning, control diazepam-treated rats showed shortened preconvulsive latencies (indicating tolerance), while BPC-157 groups maintained longer latencies with prolonged residual anticonvulsive activity
BPC-157 shows protective effects on the stomach lining by supporting mucosal integrity and promoting healing of ulcers in gastrointestinal models
The weekly total assumes the five weekday doses in the schedule, so adding both weekend doses takes it to 350 700 mg
Experiments using FITC-phalloidin staining have revealed that BPC-157 is a potent stimulator of F-actin formation in fibroblasts [11]
It should not be used as a human, veterinary, or model-animal dosing guide
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