Gw. Tang et al., GASTRIC-ACIDITY INFLUENCES THE BLOOD RESPONSE TO A BETA-CAROTENE DOSEIN HUMANS, The American journal of clinical nutrition, 64(4), 1996, pp. 622-626
The effect of gastric acidity on the blood response to a single dose o
f 120 mg beta-carotene in humans was investigated in 12 normal subject
s (5 women, 7 men) aged 23-68 y. Omeprazole was used for 7 d to oblite
rate gastric acid secretion and to raise gastric pH to > 4.5. In a cro
ssover design, six subjects were randomly assigned to take beta-carote
ne with omeprazole either at the beginning (day 9) or at the end (day
26) of the study. The beta-carotene response in blood was not altered
by the experimental order. Results from the high-gastric-pH phase (ie,
with omeprazole) were analyzed together and compared with the results
from the low-gastric-pH phase (ie, without omeprazole). The increases
of serum concentrations of both trans beta-carotene and cis beta-caro
tene 6 and 24 h after the beta-carotene dose were significantly greate
r at a low gastric pH (pH = 1.3 +/- 0.1, ie, without omeprazole) than
those at a high gastric pH (pH = 6.4 +/- 0.3, ie, with omeprazole), P
< 0.02. Similarly, 24 h after beta-carotene administration, the area u
nder the blood beta-carotene response curve (trans plus cis beta carot
ene) was significantly greater at a low gastric pH (6825 +/- 760 nmol
. h/L) than at a high gastric pH (3390 +/- 550 nmol . h/L), P < 0.002.
In investigations of bacterial overgrowth, gelatin capsule disintegra
tion and isomeric profiles associated with high and low pH, we could n
ot identify factors to explain the differences observed in the blood r
esponse curves between low-gastric-pH and high-gastric-pH conditions.
A suppressed blood response of beta-carotene at a high intraluminal pH
may have been due to the slower movement of negatively charged micell
es through the unstirred water layer and cell membrane.