How can you die early
if your mother fed adequate protein in pregancy period?? Foetal
programming of etilogy of diabetes?? Recent studies show that hepatic
metabolism and even longevity of a person can be
programmed by events during early life. The hepatic metabolism and even longevity of
a person can be programmed by events during early foetal life which is
programmed chiefly by maternal nutrition ..
How important is maternal nutrition in prepregnancy period
and in pregancy period??
Ans:-Fetal growth and development is understandably dependent
upon the nutritional, hormonal and metabolic environment provided by the
mother. Any disturbance in this environment can modify early fetal development
with possible long-term outcomes as demonstrated by extensive work on
‘programming’. Growth restriction resulting from a deficit in tissue/organ cell number (as
measured by tissue DNA content) is irrecoverable. However, when the cell size (or cell protein content) is reduced, the
effects on growth may not be permanent.
There is a strong statistical association between these
indices of early development and diseases in later life. It has been hypothesized
that the processes explaining these associations involve adaptive changes in fetal organ development in response
to maternal and fetal malnutrition. These adaptations may permanently
alter adult metabolism in a way which is beneficial to survival under continued
conditions of malnutrition but
detrimental when nutrition is abundant.
- It
is presumed that there is permanent
growth retardation in offspring where mother ingested a low-protein diet.
- (ii)
Permanent and selective changes in organ growth. Essential organs like the brain and lungs are
relatively protected from reduction in growth at the expense of
visceral organs such as the liver, pancreas, muscle and spleen.
- (iii)
Programming of liver metabolism as reflected by permanent changes in
activities of key hepatic enzymes of glycolysis and gluconeogenesis
(glucokinase and phosphoenolpyruvate carboxykinase) in a direction which
would potentially bias the liver towards a ‘starved’ setting. We have
speculated that these changes could be a result of altered periportal and
perivenous regions of the liver which may also affect other aspects of
hepatic function.
- (iv)
Deterioration in
glucose tolerance with age.
- (v)
An increase in the life span of offspring exposed to maternal protein
restriction only during the lactation period, and a decrease in life span
when exposed to maternal protein restriction only during gestation.
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