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too much protein and fat causes insulin resistance

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This article originally posted April 21, 2009 and appeared in

Issue 465

Too Much Protein or Too Many Carbs?

Why is it that not everybody who is overweight develops diabetes, and not

every person with diabetes is overweight? That's where the disease gets

complicated

The next time you grab a glass full of protein shake remember this

admonition: too much protein, eaten along with fat, may lead to insulin

resistance.

In a paper published last week, Duke University researchers describe a new

finding that indicates diabetes could be affected by protein - not the usual

suspects of sugary carbohydrates. The Duke team found that obese people

metabolize protein differently than lean people, particularly when it's part

of

a high-fat diet.

When people eat too much protein and fat - think double cheeseburger - the

metabolic byproducts can't be fully absorbed, and they flood the

bloodstream.

Among those byproducts is an enzyme that affects insulin sensitivity. As a

result, a diet heavy on Big Macs creates a whole new way for the body to

become

insulin-resistant.

The study was led by Newgard of Duke Medical Center who reported

that rats fed high-fat (HF) diets supplemented with extra so-called branched

chain amino acids (BCAA) don't have to eat as much or gain as much weight to

develop insulin resistance as do chubbier animals fed a high-fat diet alone.

Moreover, those ill effects of branched chain amino acids, which include 3

of the 20 amino acids that are the building blocks of proteins, occurred

only

in the context of a high-fat diet.

" We've all made a big deal out of the fact that people in the U.S. eat too

much fat and sugar, but we've underestimated the protein component, " Newgard

said.

And indeed, he said, surveys have shown that most people who overeat don't

show any particular prejudice toward one food group or another.

By comparing the metabolic profiles of obese versus lean people in the new

study, the researchers found that key among the many differences between the

two groups were elevated levels of BCAA in those who were overweight.

They also showed that BCAA tend to climb along with insulin resistance, a

condition that is a precursor to diabetes. To further explore that

correlation,

they turned to studies of rats. Those controlled feeding studies revealed

that, despite having reduced food intake and a low rate of weight gain

equivalent

to animals on standard chow, rats that consume more fat and BCAA were as

insulin resistant as rats fed an HF diet. When added to a normal mouse diet,

extra

BCAA didn't result in insulin resistance.

The insulin resistance in the animals eating extra fat and BCAA was

accompanied by changes in molecular players in the insulin signaling

pathway, they report.

The ill effects of BCAA in combination with high fat might be explained in

part by a buildup of chemicals known as acylcarnitines in the animals'

skeletal

muscles, the researchers suggest. Consistent with their prior studies, they

report that high-fat feeding caused significant accumulation of multiple

acylcarnitines

in muscle relative to the standard chow or standard chow plus BCAA groups.

" Surprisingly, " they report, " the HF/BCAA diet caused accumulation of the

same array of muscle acylcarnitines, despite the fact that the HF/BCAA

animals

weighed less and consumed less food than the HF-fed animals. "

HF/BCAA feeding also led to levels of certain acylcarnitines exceeding those

in animals in all other feeding groups.

Overall, the results suggest that " in the context of a dietary pattern that

includes high-fat consumption, BCAA may make an independent contribution to

development of insulin resistance and diabetes, " they concluded.

Practice Pearls:

Explain to interested patients that the adverse impact of a high-fat diet on

insulin sensitivity is well known

Note that this study suggests that a diet including fat and branched-chain

amino acids -- found in dairy product and meats -- may also induce insulin

resistance

Cell Metabolism, April 2009

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