» Articles » PMID: 27882216

Intake of Kale Suppresses Postprandial Increases in Plasma Glucose: A Randomized, Double-blind, Placebo-controlled, Crossover Study

Overview
Journal Biomed Rep
Specialty Biochemistry
Date 2016 Nov 25
PMID 27882216
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Kale ( var. ), a vegetable in the family Brassicaceae, has beneficial effects on health, including hypoglycemic effects. In our previous study with a limited number of subjects, intake of kale-containing food at a dose of 14 g decreased postprandial plasma glucose levels. In the present study, the effective dose of kale-containing food was investigated in a randomized, double-blind, placebo-controlled, crossover trial. The trial was conducted on 42 Japanese subjects aged 21-64 years with fasting plasma glucose levels of ≤125 mg/dl and 30-min postprandial plasma glucose levels of 140-187 mg/dl. The subjects consumed placebo or kale-containing food [7 or 14 g; low-dose (active-L) or high-dose (active-H) kale, respectively] together with a high-carbohydrate meal. At 30-120 min after the test meal intake, the plasma levels of glucose and insulin were determined. The postprandial plasma glucose levels in subjects with intake of active-L or active-H were significantly lower than those in subjects with intake of placebo, with the maximum plasma concentration (C; 163±24 mg/dl for active-L and 162±23 mg/dl for active-H compared with 176±26 mg/dl for placebo [values presented as means ± standard deviation (SD); P<0.01]. The area under the plasma glucose concentration-time curve for 0-2 h (AUC) values (means ± SD) were significantly lower for active-L (268±43 mg/h/dl) and active-H (266±42 mg/h/dl) than for the placebo (284±43 mg/h/dl; P<0.05). No significant differences were identified in the postprandial plasma insulin levels between the three conditions. No adverse events associated with intake of either dose of kale were observed. Our findings suggest that intake of kale suppresses postprandial increases in plasma glucose levels at a single dose of 7 g, and that a dose as high as 14 g is safe.

Citing Articles

Effects of incorporating green leafy vegetables with meals on starch and lipid digestibility under simulated gastrointestinal digestion.

Kaewpradup T, Kamonsuwan K, Chusak C, Siervo M, Adisakwattana S Sci Rep. 2025; 15(1):5282.

PMID: 39939724 PMC: 11822116. DOI: 10.1038/s41598-025-89573-1.


Beneficial Effects of a Freeze-Dried Kale Bar on Type 2 Diabetes Patients: A Randomized, Double-Blinded, Placebo-Controlled Clinical Trial.

Jeppesen P, Dorner A, Yue Y, Poulsen N, Andersen S, Aalykke F Nutrients. 2024; 16(21).

PMID: 39519473 PMC: 11547987. DOI: 10.3390/nu16213641.


Before or Concomitant Drinking Greenleaf Juice with Rice Reduces Postprandial Blood Glucose Levels in Healthy Young Women.

Sera N, Taguchi F, Hanamura I, Hongo R Nutrients. 2024; 16(19).

PMID: 39408193 PMC: 11478157. DOI: 10.3390/nu16193226.


Is freeze-dried superfood kale supplementation healthier than common green peas? Outcomes of a cross-over trial.

Aldisi D, Sabico S, Almiman A, Al-Farraj A, Basaeed T, Wani K Front Nutr. 2024; 11:1370677.

PMID: 39114118 PMC: 11303336. DOI: 10.3389/fnut.2024.1370677.


Improving the Health-Benefits of Kales ( L. var. DC) through the Application of Controlled Abiotic Stresses: A Review.

Ortega-Hernandez E, Antunes-Ricardo M, Jacobo-Velazquez D Plants (Basel). 2021; 10(12).

PMID: 34961097 PMC: 8706317. DOI: 10.3390/plants10122629.

References
1.
Grundy S . Pre-diabetes, metabolic syndrome, and cardiovascular risk. J Am Coll Cardiol. 2012; 59(7):635-43. DOI: 10.1016/j.jacc.2011.08.080. View

2.
Sikora E, Bodziarczyk I . Composition and antioxidant activity of kale (Brassica oleracea L. var. acephala) raw and cooked. Acta Sci Pol Technol Aliment. 2012; 11(3):239-48. View

3.
Ramachandran A, Snehalatha C, MARY S, Mukesh B, Bhaskar A, Vijay V . The Indian Diabetes Prevention Programme shows that lifestyle modification and metformin prevent type 2 diabetes in Asian Indian subjects with impaired glucose tolerance (IDPP-1). Diabetologia. 2006; 49(2):289-97. DOI: 10.1007/s00125-005-0097-z. View

4.
Tabak A, Herder C, Rathmann W, Brunner E, Kivimaki M . Prediabetes: a high-risk state for diabetes development. Lancet. 2012; 379(9833):2279-90. PMC: 3891203. DOI: 10.1016/S0140-6736(12)60283-9. View

5.
Heianza Y, Hara S, Arase Y, Saito K, Fujiwara K, Tsuji H . HbA1c 5·7-6·4% and impaired fasting plasma glucose for diagnosis of prediabetes and risk of progression to diabetes in Japan (TOPICS 3): a longitudinal cohort study. Lancet. 2011; 378(9786):147-55. DOI: 10.1016/S0140-6736(11)60472-8. View