High plasma free fatty acids decrease splanchnic glucose uptake in patients with non-insulin-dependent diabetes mellitus

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Abstract

It has been proposed that high plasma free fatty acid (FFA) levels observed in patients with non-insulin dependent diabetes mellitus (NIDDM) contribute to the development of their insulin resistance. We examined patients with NIDDM to find whether maintaining plasma FFA levels in the fasting range with a euglycemic hyperinsulinemic clamp combined with an oral glucose load (clamp OGL) would affect insulin-mediated peripheral glucose uptake (PGU) and splanchnic glucose uptake (SGU). Nine NIDDM subjects (age, 55 ± 3 years; duration of diabetes, 11 ± 2 years; body mass index, 21.0 ± 0.4 kg/m2; hemoglobin A1c, 9.0 ± 0.3%; fasting plasma glucose, 9.4 ± 3.0 mmol/l, means ± SEM) were hospitalized and treated with diet, oral hypoglycemic agents or insulin for at least 2 weeks to maintain fasting plasma glucose < 8 mmol/l. All the patients were subjected to two different protocols in a random order. On one protocol, under the hyperinsulinemic condition, FFAs were maintained at the their fasting levels (1.19 ± 0.08) by triglyceride emulsion infusion (Lipid infusion study, L), and on the other protocol, FFAs were made to fall (0.26 ± 0.06 mmol/l) with saline instead of triglyceride emulsion infusion (Saline infusion study, S). During euglycemic (L, 5.4 ± 0.2; S, 5.1 ± 0.2 mmol/l) hyperinsulinemic (L, 1377 ± 108; S, 1328 ± 67 pmol/l) clamp, high FFA levels significantly reduced PGU (L, 26.7 ± 3.6; S, 32.1 ± 3.4 μmol · kg-1-min-1, P<0.05) and SGU (L, 12.1 ± 4.2; S, 27.5 ± 5.6%, P<0.05). In conclusion, high FFA levels in patients with NIDDM impaired insulin-mediated glucose uptake in the splanchnic as well as peripheral tissues.

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Tomita, T., Yamasaki, Y., Kubota, M., Tohdo, R., Katsura, M., Ikeda, M., … Hori, M. (1998). High plasma free fatty acids decrease splanchnic glucose uptake in patients with non-insulin-dependent diabetes mellitus. Endocrine Journal, 45(2), 165–173. https://doi.org/10.1507/endocrj.45.165

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