A popular fermented soybean food of Northeast India exerted promising antihyperglycemic potential via stimulating PI3K/AKT/AMPK/GLUT4 signaling pathways and regulating muscle glucose metabolism in type 2 diabetes.

This study examined the antidiabetic efficacy of popular fermented soybean foods (FSF) of Northeast (NE) India. Results showed that among different FSF, aqueous extract of Hawaijar (AEH), a traditional FSF of Manipur, NE India, significantly augmented glucose utilization in cultured myotubes treated with high glucose (HG, 25 mM). Furthermore, AEH also upregulated glucose uptake, glucose-6-phosphate level, and phopho-PI3K/phospho-AKT/phospho-AMPK/GLUT4 protein expression in HG-treated myotubes. In vivo studies demonstrated that AEH supplementation (50, 100, or 200 mg/kg body weight/day, oral gavaging, 16 weeks) reduced body weight, fasting blood glucose, glycated hemoglobin, insulin resistance, and glucose intolerance in rats fed with high-fat diet (HFD). AEH supplementation stimulated phopho-PI3K/phospho-AKT/phospho-AMPK/GLUT4 signaling cascades involved in glucose metabolism of muscle tissues in diabetic rats. Chemical profiling of AEH (SDS-PAGE, immunoblotting, and HRMS) suggests the possible role of bioactive proteins/peptides and isoflavones underlying the antihyperglycemic potential AEH. Results from this study will be helpful for developing food-based prophylactics/therapeutics in managing hyperglycemia. PRACTICAL APPLICATIONS: Fermented soybean foods are gaining acceptance due to multiple health benefits. This study for the first time reports the antidiabetic potential of Hawaijar, an indigenous fermented soybean food of North-East India. Higher abundance of bioactive compounds (isoflavones and proteins/peptides) in Hawaijar may be responsible for the alleviation of impaired glucose metabolism associated with diabetes. The findings may be helpful for the development of a novel therapeutic to achieve better control of hyperglycemia and improve the lives of the patient population with diabetes.

[1]  Zuhair M. Mohammedsaleh,et al.  Decapeptide from Potato Hydrolysate Induces Myogenic Differentiation and Ameliorates High Glucose-Associated Modulations in Protein Synthesis and Mitochondrial Biogenesis in C2C12 Cells , 2022, Biomolecules.

[2]  J. Jia,et al.  Butyrate ameliorates skeletal muscle atrophy in diabetic nephropathy by enhancing gut barrier function and FFA2‐mediated PI3K/Akt/mTOR signals , 2021, British journal of pharmacology.

[3]  Uttam Pal,et al.  Evaluation of therapeutic effect of Premna herbacea in diabetic rat and isoverbascoside against insulin resistance in L6 muscle cells through bioenergetics and stimulation of JNK and AKT/mTOR signaling cascade. , 2021, Phytomedicine : international journal of phytotherapy and phytopharmacology.

[4]  Prasenjit Manna,et al.  Beneficial effect of the methanolic leaf extract of Allium hookeri on stimulating glutathione biosynthesis and preventing impaired glucose metabolism in type 2 diabetes. , 2021, Archives of biochemistry and biophysics.

[5]  Xinli Hu,et al.  Negative regulation of AMPK signaling by high glucose via E3 ubiquitin ligase MG53. , 2020, Molecular cell.

[6]  Prasenjit Manna,et al.  Gamma‐glutamyl–carboxylated Gas6 mediates positive role of vitamin K on lowering hyperglycemia in type 2 diabetes , 2020, Annals of the New York Academy of Sciences.

[7]  W. Luo,et al.  High glucose inhibits myogenesis and induces insulin resistance by down-regulating AKT signaling. , 2019, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[8]  C. Witczak,et al.  Regulation of Skeletal Muscle Glucose Transport and Glucose Metabolism by Exercise Training , 2019, Nutrients.

[9]  Prasenjit Manna,et al.  Daidzein, its effects on impaired glucose and lipid metabolism and vascular inflammation associated with type 2 diabetes , 2018, BioFactors.

[10]  Guihua Liu,et al.  The PI3K/AKT pathway in obesity and type 2 diabetes , 2018, International journal of biological sciences.

[11]  Prasenjit Manna,et al.  Prophylactic role of vitamin K supplementation on vascular inflammation in type 2 diabetes by regulating the NF-κB/Nrf2 pathway via activating Gla proteins. , 2018, Food & function.

[12]  Nadeem Shafique Butt,et al.  Effect of diet on type 2 diabetes mellitus: A review , 2017, International journal of health sciences.

[13]  A. Rai,et al.  Production of bioactive peptides during soybean fermentation and their potential health benefits , 2016 .

[14]  C. Lammi,et al.  Three Peptides from Soy Glycinin Modulate Glucose Metabolism in Human Hepatic HepG2 Cells , 2015, International journal of molecular sciences.

[15]  G. Vistoli,et al.  Two Peptides from Soy β-Conglycinin Induce a Hypocholesterolemic Effect in HepG2 Cells by a Statin-Like Mechanism: Comparative in Vitro and in Silico Modeling Studies. , 2015, Journal of agricultural and food chemistry.

[16]  V. Ramachandran,et al.  Glucose uptake through translocation and activation of GLUT4 in PI3K/Akt signaling pathway by asiatic acid in diabetic rats , 2015, Human & experimental toxicology.

[17]  J. Tamang Naturally fermented ethnic soybean foods of India , 2015 .

[18]  M. Ibrahim,et al.  Glycolysis, tumor metabolism, cancer growth and dissemination. A new pH-based etiopathogenic perspective and therapeutic approach to an old cancer question , 2014, Oncoscience.

[19]  T. Yonezawa,et al.  Daidzein promotes glucose uptake through glucose transporter 4 translocation to plasma membrane in L6 myocytes and improves glucose homeostasis in Type 2 diabetic model mice. , 2014, The Journal of nutritional biochemistry.

[20]  Prasenjit Manna,et al.  L‐cysteine and hydrogen sulfide increase PIP3 and AMPK/PPARγ expression and decrease ROS and vascular inflammation markers in high glucose treated human U937 monocytes , 2013, Journal of cellular biochemistry.

[21]  Yizhen Wang,et al.  Soybean glycinin- and β-conglycinin-induced intestinal immune responses in a murine model of allergy , 2013 .

[22]  E. Gilbert,et al.  Anti-diabetic functions of soy isoflavone genistein: mechanisms underlying its effects on pancreatic β-cell function. , 2013, Food & function.

[23]  L. Ghimire,et al.  A Review about the Effect of Life style Modification on Diabetes and Quality of Life , 2012, Global journal of health science.

[24]  D. Kwon,et al.  Antidiabetic effects of fermented soybean products on type 2 diabetes. , 2010, Nutrition research.

[25]  M. Berhow,et al.  Protein hydrolysates from beta-conglycinin enriched soybean genotypes inhibit lipid accumulation and inflammation in vitro. , 2009, Molecular nutrition & food research.

[26]  J. Ahn,et al.  Genistein-derivatives from Tetracera scandens stimulate glucose-uptake in L6 myotubes. , 2009, Biological & pharmaceutical bulletin.

[27]  C. Beauséjour,et al.  Blockade of sensory abnormalities and kinin B(1) receptor expression by N-acetyl-L-cysteine and ramipril in a rat model of insulin resistance. , 2008, European journal of pharmacology.

[28]  J. Frías,et al.  Immunoreactivity reduction of soybean meal by fermentation, effect on amino acid composition and antigenicity of commercial soy products. , 2008, Food chemistry.

[29]  M. Lewis,et al.  Emulsifying properties of soy protein isolate fractions obtained by isoelectric precipitation , 2001 .

[30]  H. Tsuji,et al.  Reduction of the Soybean Allergenicity by the Fermentation with Bacillus natto , 1995 .

[31]  Khee Choon Rhee,et al.  Functional properties of proteolytic enzyme modified soy protein isolate , 1990 .

[32]  G. Grant Anti-nutritional effects of soyabean: a review. , 1989, Progress in food & nutrition science.