We all know that common approaches to dieting
don’t work. This is partly because they are, no matter how they wrap it
up, still based on the overly simplistic and erroneous
notion of ‘calorie balance'. It’s a lot more complicated than that, and
if you go down that path, then you’ll continually struggle to control
your weight (fat). A new piece of research has given us a glimpse into
one mechanism that is part of this problem.
Imagine you are
driving a car, and the harder you press on the accelerator, the harder
an invisible foot presses on the brake. That's what happens when people
diet – the less food they eat, the less energy they use, and the less
fat they lose.
Neuropepetide Y (NPY) is best known for its
powerful stimulation of food intake and its effects on reducing energy
expenditure; this has been known for a good while now, but we didn’t
quite know how it worked. Now thanks to the scientists at Sydney's
Garvan Institute of Medical Research and the University of NSW we have a
better understanding.
When you don't eat, or dramatically
curtail your energy intake, levels of NPY rise sharply. High levels of
NPY signal to the body that it is in 'starvation mode' and should try to
replenish and conserve as much energy as possible. As a result, the
body reduces processes that are not absolutely necessary for survival.
In a nutshell, your hunger drive goes into overdrive, your heat output
is reduced and your libido and general energy levels get pummelled.
The researchers found that NPY produced in a particular region of the
brain called the ‘arcuate nucleus (Arc) of the hypothalamus’ inhibits
the activation of 'brown fat', one of the primary tissues where the body
generates heat (*see links below). This study is the first to identify
the neurotransmitters and neural pathways that carry signals generated
by NPY in the brain to brown fat cells in the body. It is also the first
to show a direct connection between Arc NPY, the sympathetic nervous
system and the control of energy expenditure.
Reference:
Yan-Chuan Shi et al. Arcuate NPY Controls Sympathetic Output and BAT
Function via a Relay of Tyrosine Hydroxylase Neurons in the PVN. Cell
Metabolism, Volume 17, Issue 2, 236-248, 5 February 201
* http://humanperformanceconsulting-uk.blogspot.co.uk/2011/11/hpc-uks-top-tips-for-fat-loss-tip-no9.html
* http://humanperformanceconsulting-uk.blogspot.co.uk/2012/01/ive-got-chills-theyre-multiplying.html
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