Table 3.
Description of the principal clinical effects of hop isomerized compounds.
Compound | Clinical Investigation | Biological Effect | Ref. | |
---|---|---|---|---|
Dose | Time of Treatment | |||
Iso-humulone | 16–32–48 mg 80mg |
12 weeks 8 weeks |
↓body weight ↓total fat area ↓BMI ↓fasting blood glucose ↓HbA1c ↓systolic blood pressure ↓GPT, GOT, GTP blood levels |
[24,26,65] |
IHE | Capsules containing 10.8 mgIHE/10 kg body weight | 30 and 120 min after ingestion | ↓triglyceride levels ↓glucose levels ↓insulin levels ↑FDM ↑NO ratio |
[12] |
Bitter hop extract | 100 or 250 mg | 24 h | ↓hunger reduction | [66] |
KDT501 | escalating doses from 200 to a maximum dose of 1000 mg every 12 h | From 7 days to 28 days | ↓total cholesterol ↓post-meal triglycerides ↑adiponectin ↓TNF-α ↓ACACA mRNA expression ↓DGAT mRNA expression |
[69] [70] |
THIAA | 940 mg | Single oral dose | ↓systematic inflammation ↓TNF-α ↓IL-6 |
[53] |
RIAA | 600 mg 500 mg 450 mg |
Single oral dose 6 weeks 14 days |
↓iCOX-2 ↓PGE2 ↓WOMAC Global score ↓VAS score ↓CYP2C9 (IC50 = 0,25 µg/mL) ↓CYP2C19 (IC50 = 6.1 µg/mL) ↑PGI-M/TXB2 ratio |
[59,72] |
Abbreviations: Rho-iso-α-acids RIAA; Tetrahydro-iso-α-acids THIAA; Potassium salt of the n-(isobutyl) congener of a tetrahydro iso-α-acid KDT501.