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The effects of palmitate and chicoric acid on diabetes

Investigation the effects of palmitate and cichoric acid on inflammation pathway in PBMCs of type2 diabetic patient and control group

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017071535085N1
Enrollment
40
Registered
2017-08-02
Start date
2017-09-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Group (4) treatments with palmitate (500 µM) plus chicoric acid (50 µM), the cells of this group are treated with palmitate at a concentration of 500 µM for 24 hours. Then, they are tr
Treatment - Drugs
Group (4) treatments with palmitate (500 µM) plus chicoric acid (50 µM), the cells of this group are treated with palmitate at a concentration of 500 µM for 24 hours. Then, they are treated with chico
Separation of the cells is according to the ficole protocol. In the next step, cell pellets are suspended in the 2 cc culture medium and cell count evaluates using trypan blue. The cells are cultured
Group (3) treatment with chicoric acid at a concentration of 50 µM. The chicoric acid was dissolved in dimethyl sulfoxide and then reached the desired volume using the culture medium. The cells of th
Group (2) treatment with palmitate with a concentration of 500 µM. Sodium palmitate was dissolved in 50% ethanol at 55 °C. Then, using a culture medium containing bovine serum albumin 1% reached th

Sponsors

Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: FBS greater than 126 mg/dL; 2 hours blood glucose greater than 200 mg/dl; HbA1C greater than 6.5%; The control group should have a fasting blood glucose less than 100 mg/dl. Exclusion criteria: Use of medications such as antihypertensive drugs (such as beta-blockers), anti-diabetic drugs, estrogen supplements, thyroxine, diuretics and hypolipemic drugs; Other chronic and acute inflammatory diseases such as chronic kidney disease, cardiovascular disease, hypertension and ...; Infectious diseases, cancer, allergies; Other Endocrine Disorders (Except Type 2 Diabetes); Pregnancy; Smoking

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
SIRT1. Timepoint: One day after the intervention, Two day after the intervention. Method of measurement: Gene expression of SIRT1 using Ct of gene.;IL-6. Timepoint: One day after the intervention, Two day after the intervention. Method of measurement: Gene expression of IL-6 using Ct of gene.;P-AMPK. Timepoint: One day after the intervention, Two day after the intervention. Method of measurement: concentration of p-AMPK using western blotting.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Ziamajidi

Hamadan University of Medical Sciences

n_ziamajidi@yahoo.com, n.majidi@umsha.ac.ir+98 912 672 2548

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026