View Single Post
Old 09-18-2007, 02:52 AM   #4
fullofbeans
Senior Member
 
Join Date: Jan 2007
Location: UK
Posts: 617
Although referred as sugars there are different types: mainly glucose, fructose and galactose. The glucose itself can have various structure. Glucose can be absorbed by every cells whereas fructose has to be metabolised by the liver first. the liver will drop everything it is doing to metabolise fructose. Refined sugar (sucrose=glucose+fructose) are 'absorbed' quickly produces and as a result produces a sharp rise in your blood sugar and impact on insuline production; Their Glycemic Index reflect this.

However the GI index is not really appropriate to see the effect of fructose on the blood sugar (since GI is standardised for glucose). However studies have shown that fructose increases the blood sugar by almost as much as glucose:

A good paper to read to understand the fructose vs glucose:
http://www.obesityresearch.org/cgi/c...2/suppl_2/124S

Another interesting paper:

http://www.ajcn.org/cgi/content/abstract/49/4/658

Basically if you think that refined sugar is poison and feeds cancer then perhaps you should extend this to fruits, .., except that at least with fruit you are getting anti oxidant & enzymes that are good for you.

The quoted 110mg is first thing in the morning (before breakfast) which is often referred as the fasting blood sugar, the lowest blood sugar level of the day. But it is not trully the fasting (absence of food) amount (which occur after 24hr after the last meal, once your liver has use its stock of glycogen). The fasting blood sugar is then around 50-70.

Anyhow since we talking about sugars I now use what I think is a better alternative for sugar than Stivia (which I do not like so much ): Xylitol which taste great is natural and comes with an array of good side effect from being tooth friendly& prevent weakening of the bone

http://en.wikipedia.org/wiki/Xylitol


Hope this help
__________________

35 y/o
June 06: BC stage I
Grade 3; ER/PR neg
Her-2+++; lumpectomies

Aug 06: Stage IV
liver mets: 6 tumours
July 06 to Jan 07: 2*FEC+6*Taxotere; 3*TACE; LITT
March 07- Sept 07: Vaccination trial (phase 2, peptide based) at the UW (Seattle).
Herceptin since 2006
NED til Oct 09
Recurrence Oct 2009: to internal mammary gland since October 2009 missed on Oct and March 2010 scan.. palpable nodes in May 2010 when I realised..
Nov 2011:7 mets to lungs progressing fast failed hercp/tykerb/xeloda combo..

superior vena cava blocked: stent but face remains puffy

April 2012: Teresa Trial, randomised to TDM1
Nov 2012 progressing on TDM1
Dec 2012 blockage of my airways by tumours, obliteration of these blocking tumours breathing better but hoping for more- at mo too many tumours to count in the lungs and nodes.

Dec 2012 Starting new trial S-222611 phase 1b dual egfr her2+ inhibitor.



'Under no circumstances should you lose hope..' Dalai Lama
fullofbeans is offline   Reply With Quote