Dihydroberberine Powder Manufactury,1kg Dihydroberberine Powder,Bulk Dihydroberberine Powder
Dihydroberberine Description
Dihydroberberine, abbreviated as DHB, CAS number 483-15-8, is the reduced metabolic form of the traditional Chinese medicine component berberine. Dihydroberberine appears as a yellow crystalline powder. Compared to traditional berberine, dihydroberberine powder exhibits superior bioavailability and absorption.
In the latter half of 2022, a consumer documented their weight loss journey using berberine on TikTok, propelling this ingredient to viral fame online. Berberine, or dihydroberberine, gained recognition as a natural weight loss product.
Function
Berberine promotes transcription of the glucagon-like peptide-1 receptor gene and enhances proliferation of intestinal L cells, while also increasing GLP-1 secretion.
It activates the bitter taste receptor TAS2R38 in the intestine, thereby triggering L cells to release GLP-1.
Berberine regulates blood glucose metabolism by inhibiting hepatic gluconeogenesis.
Berberine promotes energy expenditure and benefits intestinal metabolism.
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Dihydroberberine Powder Factory
Dihydroberberine Powder Manufacturer Direct Supply. Our Dihydroberberine offers consistent quality. Jinan Sinov provides 1kg Dihydroberberine Powder in premium packaging, ideal for laboratory research or sample testing. We also support bulk Dihydroberberine Powder supply for factory production and long-term procurement.
Reference:
YU Y, HAO G, ZHANG Q, et al. Berberine induces GLP-1 secretion through activation of bitter taste receptor pathways [J]. Biochem Pharmacol, 2015, 97(2): 173-7.
XIA X, YAN J, SHEN Y, et al. Berberine improves glucose metabolism in diabetic rats by inhibition of hepatic gluconeogenesis [J]. PLoS One, 2011, 6(2): e16556.
REN G, GUO J H, QIAN Y Z, et al. Berberine Improves Glucose and Lipid Metabolism in HepG2 Cells Through AMPKalpha1 Activation [J]. Front Pharmacol, 2020, 11: 647.
ZHU X, BIAN H, WANG L, et al. Berberine attenuates nonalcoholic hepatic steatosis through the AMPK-SREBP-1c-SCD1 pathway [J]. Free Radic Biol Med, 2019, 141: 192-204.
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