Effect of goat milk protein hydrolysates on antidiabetic activity and its insulin resistance in HepG2 cells

Authors

  • Nouran Hussein Dairy Unit, Department of Animal Breeding, Desert Research Center, Matariya, 11753, Cairo, Egypt.
  • K.A. Soryal Dairy Unit, Department of Animal Breeding, Desert Research Center, Matariya, 11753, Cairo, Egypt.
  • M.A. El- Nawawy Food Science. Department, Faculty of. Agriculture, Ain Shams University, P.O. Box 68, Hadayek Shoubra 11241, Cairo, Egypt.
  • I.E. Aumara Food Science. Department, Faculty of. Agriculture, Ain Shams University, P.O. Box 68, Hadayek Shoubra 11241, Cairo, Egypt.

Keywords:

Goat milk protein hydrolysates, Proteolytic enzymes, Diabetes, α-amylase activity, Insulin resistance, HepG2 cells

Abstract

Goat milk protein hydrolysates (Acid casein, Rennet casein, and Total milk protein) were prepared using different proteolytic enzymes (pancreatin, pepsin, and trypsin) throughout 8 hrs of hydrolysis time. The degree of hydrolysis (DH) of goat milk protein hydrolysate was estimated by OPhthaldialdehyde (OPA) method at different hydrolysis times (0, 1, 2, 4, 6, and 8 hrs). The effect of different three types of goat milk protein hydrolysates on antidiabetic activity was investigated by testing the inhibition of α-amylase activity and glucose consumption rate in HepG2 cells. The types of goat milk protein hydrolysates, proteolytic enzymes, and hydrolysis time had a significant effect on DH. The highest DH was in rennet casein hydrolysates treated with pancreatin enzyme at 8 hrs, followed by acid casein hydrolysates treated with pancreatin enzyme at 6 and 8 hrs. While TMP hydrolysates treated with pepsin enzyme had the highest DH at 4 hrs. The highest hydrolysis time was at 2, 4, and 8 hrs by trypsin, pepsin, and pancreatin enzymes, respectively. The rennet casein hydrolysates by the pancreatin enzyme had the highest anti-diabetic impact of exhibiting its action by inhibiting the
enzymes which have the main role in carbohydrate metabolism as the α-amylase enzyme and dramatically increased the glucose consumption rate in insulin-resistant HepG2 cells, followed by TMP hydrolysate treated with pepsin enzyme.

Published

30.06.2023