TY - JOUR
T1 - D-chiro-Inositol is absorbed but not synthesised in rodents
AU - Lin, Xiaobo
AU - Ma, Lina
AU - Gopalan, Chaya
AU - Ostlund, Richard E.
PY - 2009/11
Y1 - 2009/11
N2 - d-chiro-inositol (DCI) and pinitol (1d-3-O-methyl-chiro-inositol) are distinctive inositols reported to possess insulin-mimetic properties. DCI-containing compounds are abundant in common laboratory animal feed. By GCMS of 6m-HCl hydrolysates, Purina Laboratory Rodent Diet 5001 (diet 5001) contained 0.23% total DCI by weight with most found in the lucerne and soya meal components. In contrast, only traces of l-chiro-inositol were observed. The DCI moiety was present in a water-soluble non-ionic form of which most was shown to be pinitol. To measure the absorption of dietary inositols, rats were fed diet 5001 in a balance study or given purified pinitol or [2H6]DCI. More than 98% of the total DCI fed to rats as diet 5001, purified pinitol or [ 2H6]DCI was absorbed from the gastrointestinal tract. Rats chronically on diet 5001 consumed 921mol total DCI/kg body weight per d but excreted less than 5.3% in the stools and urine, suggesting that the bulk was metabolised. The levels of pinitol or DCI in plasma, stools or urine remained relatively stable in mice fed Purina PicoLab® Rodent Diet 20 5053 over a 5-week period, whereas these values declined to very low levels in mice fed a pinitol/DCI-deficient chemically defined diet. To test whether DCI was synthesised or converted from myo-inositol, mice were treated with heavy water or [2H6]myo-inositol. DCI was neither synthesised endogenously from 2H-labelled water nor converted from [2H6]myo-inositol. DCI and pinitol in rodents appear to be derived solely from the diet.
AB - d-chiro-inositol (DCI) and pinitol (1d-3-O-methyl-chiro-inositol) are distinctive inositols reported to possess insulin-mimetic properties. DCI-containing compounds are abundant in common laboratory animal feed. By GCMS of 6m-HCl hydrolysates, Purina Laboratory Rodent Diet 5001 (diet 5001) contained 0.23% total DCI by weight with most found in the lucerne and soya meal components. In contrast, only traces of l-chiro-inositol were observed. The DCI moiety was present in a water-soluble non-ionic form of which most was shown to be pinitol. To measure the absorption of dietary inositols, rats were fed diet 5001 in a balance study or given purified pinitol or [2H6]DCI. More than 98% of the total DCI fed to rats as diet 5001, purified pinitol or [ 2H6]DCI was absorbed from the gastrointestinal tract. Rats chronically on diet 5001 consumed 921mol total DCI/kg body weight per d but excreted less than 5.3% in the stools and urine, suggesting that the bulk was metabolised. The levels of pinitol or DCI in plasma, stools or urine remained relatively stable in mice fed Purina PicoLab® Rodent Diet 20 5053 over a 5-week period, whereas these values declined to very low levels in mice fed a pinitol/DCI-deficient chemically defined diet. To test whether DCI was synthesised or converted from myo-inositol, mice were treated with heavy water or [2H6]myo-inositol. DCI was neither synthesised endogenously from 2H-labelled water nor converted from [2H6]myo-inositol. DCI and pinitol in rodents appear to be derived solely from the diet.
KW - Defined diets
KW - Insulin
KW - Mass spectrometry
KW - Pinitol
UR - http://www.scopus.com/inward/record.url?scp=73749084111&partnerID=8YFLogxK
U2 - 10.1017/S0007114509990456
DO - 10.1017/S0007114509990456
M3 - Article
C2 - 19586572
AN - SCOPUS:73749084111
SN - 0007-1145
VL - 102
SP - 1426
EP - 1434
JO - British Journal of Nutrition
JF - British Journal of Nutrition
IS - 10
ER -