The first primary research objective of the study is to determine whether high-fat load (150 g of fat) induces increase in hepatic fat content (HFC) three and six hours after meal in insulin-sensitive subjects with normal HFC (\<5% of fat) and in non-diabetic subjects with an increased HFC (\>5% of fat). Furthermore, the other objective of the study is to determine whether the response of HFC to a high-fat load is affected by coadministration of glucose or fructose.
The epidemic of non-alcoholic fatty liver disease (NAFLD) is becoming a major challenge faced by health system worldwide. The hepatic fat comes from the major sources - non-esterified fatty acids (NEFA) released from adipose tissue, dietary fat and de novo lipogenesis. Fat accumulation in the liver then occurs when triglycerides (TG) that are formed are not rapidly enough oxidized or secreted from the liver in very low density lipoproteins (VLDL). It can be hypothesized that the capacity of the liver to eliminate TG can be overcome after high load of dietary fat. High-fat load should induce an immediate accumulation of hepatic fat that could be detected using 1H magnetic resonance spectroscopy (1H-MRS). The accumulation of liver fat can be also affected by coadministration of simple carbohydrates - glucose and fructose. The administration of these carbohydrates can have a pronounced impact on the availability of particular sources of hepatic fat.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
18
Subjects will consume dairy cream (150 g of fat) at time 0 hours.
Subjects will fast throughout the experiment.
Subjects will consume dairy cream (150 g of fat) at time 0 hours. At the same time and 2 and 4 hours later they will drink herbal tea containing 50 g of glucose.
Institute for Clinical and Experimental Medicine
Prague, Czechia
Hepatic fat content
Change in hepatic fat content as determined by proton magnetic resonance spectroscopy (%) between 0 and 6 hours
Time frame: Before time 0 hour, 3 hours, 6 hours
TG
Plasma triglyceride concentration
Time frame: before 0, 0.5, 1, 2, 2.5, 3, 4, 4.5, 5, and 6 hours
NEFA
Plasma non-esterified fatty-acid concentration
Time frame: before 0, 0.5, 1, 2, 2.5, 3, 4, 4.5, 5, and 6 hours
Glucose
Plasma glucose concentration
Time frame: before 0, 0.5, 1, 2, 2.5, 3, 4, 4.5, 5, and 6 hours
Insulin
Plasma insulin concentration
Time frame: before 0, 0.5, 1, 2, 2.5, 3, 4, 4.5, 5, and 6 hours
Glucagon
Plasma glucagon concentration
Time frame: before 0, 0.5, 1, 2, 2.5, 3, 4, 4.5, 5, and 6 hours
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Subjects will drink herbal tea containing 50 g of glucose at times 0, 2 and 4 hours.
Subjects will consume dairy cream (150 g of fat) at time 0 hours. At the same time and 2 and 4 hours later they will drink herbal tea containing 50 g of fructose.
Subjects will drink herbal tea containing 50 g of fructose at times 0, 2 and 4 hours.