Digested wheat gluten inhibits binding between leptin and its receptor

被引:7
作者
Jonsson, Tommy [1 ]
Memon, Ashfaque A. [1 ]
Sundquist, Kristina [1 ]
Sundquist, Jan [1 ]
Olsson, Stefan [2 ]
Nalla, Amarnadh [3 ,4 ]
Bauer, Mikael [5 ]
Linse, Sara [5 ]
机构
[1] Lund Univ Reg Skane, Ctr Primary Hlth Care Res, Skane Univ Hosp, Malmo, Sweden
[2] Univ Copenhagen, Dept Plant & Environm Sci, DK-1871 Frederiksberg C, Denmark
[3] Univ Copenhagen, Inst Biomed Sci, Fac Hlth & Med Sci, DK-2200 Copenhagen, Denmark
[4] Odense Univ Hosp, Danish Diabet Acad, DK-5000 Odense, Denmark
[5] Lund Univ, Dept Biochem & Struct Biol, Lund, Sweden
关键词
Gluten; Leptin; Leptin resistance; Obesity; UNDEGRADED DIETARY ANTIGEN; SIZE DISTRIBUTION; HEALTHY-ADULTS; RESISTANCE; OBESE; GLIADIN; PASSAGE; WEIGHT; BLOOD;
D O I
10.1186/s12858-015-0032-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Leptin resistance is considered a primary risk factor for obesity. It has been hypothesized that dietary cereal grain protein could cause leptin resistance by preventing leptin from binding to its receptor. Non-degraded dietary wheat protein has been found in human serum at a mean level of 41 ng/mL. Here, we report our findings from testing whether enzymatically digested gluten from wheat prevents leptin from binding to the leptin receptor in vitro. Gluten from wheat was digested with pepsin and trypsin under physiological conditions. Pepsin and trypsin activity was removed from the gluten digest with a 10 kDa spin-filter or by heat treatment at 100 degrees C for 30 min. Binding to the leptin receptor of leptin mixed with gluten digest at a series of concentrations was measured using surface plasmon resonance technology. Results: Binding of the gluten digest to the leptin receptor was not detected. Spin-filtered gluten digest inhibited binding of leptin to the leptin receptor, with 50% inhibition at a gluten digest concentration of similar to 10 ng/mL. Heat-treated gluten digest did not inhibit leptin binding. Conclusions: Digested wheat gluten inhibits binding of leptin to the leptin receptor, with half-maximal inhibition at 10 ng/mL. The inhibition is significant at clinically relevant concentrations and could therefore serve as a novel pathway to investigate to understand the molecular basis of leptin resistance, obesity and associated disorders.
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页数:5
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