Professional Documents
Culture Documents
glycemia,
Jetis J Hoist, and Ante Astrup ie, diabetes, is still not stanch-is
in the small
Joop on postpran-
ABSTRACT
dial plasma
The
concentrations
of resistant
of glucose,
(RS)
and
hormones,
and
overknown. not
intestine
on subjective 10 healthy,
sisted of 50
palatability young
starch
in cong raw
sweet-
However,
gested
nonresistant
as glucose
digly-
(5)
on 50
of healthy
cemia and
humans
insulinemia
in both
after
postprandial
the intake of
potato
starch
(54%
RS)
(R) together
with
500 g
artificially
RS
After the R meal postprandial plasma concentrations lactate, insulin, gastric inhibitory polypeptide (GIP),
compared
beneficial mechanisms
with
in the
digestible
control of to those
starch.
diabetes. exerted
Such
by
an effect
RS soluble
of RS
may dietary
may
through fiber
be
in-
Moreover,
glucagon-like peptideI , and epinephnine were significantly lower compared with after the S meal. Moreover, subjective scores for satiety and fullness were significantly lower after the R meal palatability
sion, significant the
similar
fluence the amount the diet, ie, glucose trol of glycemia The potential from
and rate of absorption of other and fat, which may be beneficial agent been
than
after may
the have
S meal. been
of digestible
Differences in these
starch
in GIP, findings.
with RS
texture,
resulted
and
in
involved
replacement reductions
of 1 g RS, has
as
in postprandial sensations
glycemia of satiety.
and Am
fermentation
and
in the
subjective
I.
ofdigestible
a weight-loss
I994;60:544-5
of RS on macnonutrient beneficial
recently
balance regulation.
on
appetite hypoth-
KEY WORDS
insulin, gastric
Potato
inhibitory
starch,
polypeptide,
appetite,
palatability,
lactate,
to weight
developed
catecholamines
is based
concepts
regulation
Introduction
Until recently, stanch was believed to be 100% digested in the small intestineindependent of the source, type, and preparation of the starch. However, within the past 10 y it has been found that, despite the fact that pancreatic a-amylase
of the ingested
of energy and macnonutrient balance. Thus, there close regulation between the bodys macronutrient three macronutnents (fat, protein, and carbohydrate)
(1 1, 12). The maintenance of the bodys relatively small carbohydrate stones seems especially crucial to overall energy balance ( I I ). Moreover, recent studies have shown that the control of appetite may be influenced by the amount of available carbohydrate in the diet ( 13, 14) and that consumption of carbohydrate (or protein) in a meal
achieve with satiation a resultant
is present
starch
in the
passes
gut in ample amounts ( I ), a fraction undigested to the large bowel (2-4). a more and or less complete of short-chain fermentation, fatty acids uptake
the
starch acid,
in the production
(15).
decreased
Increasing
amount ratio
the
amount
in the
in the
thus lead
diet
and to
of absorbed
carbohydrate
and propionic acid) (5, 6). This fraction of the starch has been named resistant starch (RS) and has been defined by the European FLAIR Concerted Action on Resistant Starch (EURESTA) the sum of starch and products of starch hydrolysis not sorbed in the small intestine of healthy individuals. The amount of RS present in starch-rich foods depends
as
a decreased
carbohydrate-to-fat
abon
Food
sity
From the Research Department of Human Nutrition. Research. The Royal Veterinary and Agricultural
Denmark: Italy: the the Department of of Internal Human Medicine Nutrition. and of Pavia, Department
Fredeniksberg.
several factors, ic, the source, ripeness, processing, preparation, and storage of the foods. It has been shown that stanch from white bread, porridge oats, and cornflakes is almost completely digested in the small intestine (4) whereas native starch from banana and uncooked potato is highly resistant to hydrolysis in vitro
(7) and in vivo (8). When the potato is cooked the starch granules
ology.
2
Henley
Supported
Hospital.
Denmark:
and
The Danish
the
Department Denmark.
Research and
of
Physiology.
Development
The Panum
Institute,
by Food
University
grants from
of Copenhagen. 1990to A
Technology
Medical
of
grant Centre
I 2-9537-3.
Raben.
Address
reprint
University.
requests
25
Human
Agricultural
Nutrition,
for Food
Rolighedsvej.
Research,
The Royal
DK-1958
Veterinary
C.
and
and reverses
become this
readily gelatinization
of the I 2% of
Frcderiksberg
Received
November
2. 1993.
resistant
to small
Accepted
1994;60:544-5 I . Printed
for publication
in USA.
May 9. 1994.
1994 American Society for Clinical Nutrition
RESISTANT TABLE
Subject
STARCH,
AND
SATIETY
545
I
characteristics Denmark
(ii
=
reference
starch
materials
Cal culated starch values
Italy 5) 1.9
3.0 1.1
(ii
=
All 5) 0.7
(ii
=
10)
Food
Age
Height Weight
DM %
TS
RDS (;y b z
SDS
RS
(y)
(m) (kg)
25.6
1.80 71.2
21.2
1.78 74.0 23.2
23.4
1.79 72.6 22.6
1.2
t 0.01
BMI2
Fat mass (%)
22.0
Raw potato
starch
83.4
95.1
81.3
92.9
6.0
87.9
21.2
5.2
54.1
-
18.6 2.4
20.8
1.3
19.7
1.3
Pregelatinizedpotatostarch
,.
SEM. In kg/m.
DM, dry matter: TS. total starch: RDS. rapidly digestible SDS, slowly digestible starch: RS. resistant starch. Analyzed Dunn Clinical Nutrition Centre. Methods described by Englyst and Englyst and Cummings (22).
starch:
a reduction
in the
satiating
power
of
the
diet.
This
may
result
in
subsequent
weight
effect in the diet
gain.
on may
However,
satiety be ( I 6beneficial
if RS
1 8) an to
positive RS
from Nantes,
while an
lInstitut France.
of
consumption
mixing increase in
The effects
changes tions of
purpose of RS
in hunger
study nonresistant
was
to investigate starch
and starches
a hand
mixer the
speed
on
glycemia,
subjective
ways meals.
were
tested
before stanch
deciding could
on these not
test
pregelatinized
as pure
se without
a form
the
as possible
interference
to clarify
from other
the
role
of the starches
pen
nutrients.
of the raw starch, a cold-meal preparation had to be used. The starches could thus not be baked into a bread or used in a pasta.
Subjects
The EURESTA ducted Nutrition, Denmark, of Pavia, Subjects In each normal-weight,
obesity or
and methods
experiment framework. at two The and Italy. centers: Royal the was performed Exactly the as a joint same study within was the con-
for these two starches was therefore to mix For the R meal this resulted in a drinkable was
syrup
whereas
Although
the S meal
the
a porridge-like
was sweetened naturally sugars
gel to be eaten
with artificial in occurring
experiment
it contained some and fruits (Table test day was preceded diet (60% of energy
and 3.5
fruit
3).
by 3 d on an identical as carbohydrate, 28%
fiber/Mi), prepared
Department
as
protein. from
g dietary
partments
center
diabetes,
five
healthy
subjects athletes)
(20-31
y of age,
nonsmokers, included
The
were
strual
not
cycle.
with no history of participated in the study (Table 1). Females to avoid possible differences due to the menenergy needs during the study were
energy subjects
food items according to each subjects individual requirements. and adjusted to the nearest 0.5 Mi. The were instructed to adhere strictly to the diet. If subjects
subjects
to age, weight, was used to acsubjects (19). The by the bioimInc. Odense) in Italy.
Deunenberg Ethical
TABLE 3 Carbohydrate
(50 g potato
and energy
starch +
contents
in the fruit
two
test
meals
500
mL diluted
syrup)
for medium
physical
Test meal R S
46.5
and
calculated study
109 (Ril
by using approved and
Systems,
the by equation the
Detroit)
of Municipal
Fat-free
et Comwith al
Total
starch
in 50 g potato
starch
(g)
40.7
of Copenhagen
Fredeniksbeng
to be in accordance
27.1
3.0
0.0
44.0 2.6
8.4
10.6
8.4
declaration
and procedure
gave
written
consent
the experimental
explained
to them.
Glucose Fructose
Sucrose(g)
2.9 4.4
1.1
2.9 4.4
1.1
The two test meals consisted RS) (R) on 50 g pregelatinized (5) mixed 2).
from
Total Total
into The
black
500
syrup
mL
current,
diluted
was based and
sweetened
grape. commercially
fruit
red
syrup
current, pun-
starch:
digestible
S. pregelatinized
starch: SDS,
starch:
digestible
(Table
elderberry, chased
starch:
2 3
Not taking
16.7 kJ/g.
fermentation
into consideration.
Irma,
Denmark.
The
starches
were
produced
and
546 could was not deducted consume from all the the diet hod, during they and had to bring the The
ET
AL centrifuged for 10 mm at 300f x g and 4 #{176}C and stoned at -80 #{176}C until determination of catecholamines method measured Novo, glucagon-like on (27-29). from and (26). Immunoreactive with Gastric I (GLPextracted for insulin radioimmunoassay inhibitory I ) were with the GIP polydeterethanol and were (GIP) by in plasma Copenhagen. peptideplasma the con-
for weighing
registration.
the following
preexpenimental
The subjects were instructed activity for the 2 d before diet this should ensure
to abstain from strenuous the test days. Together with equally filled glycogen stones
the standard
peptide
mined as GLPjects. Nutrition
scnibed
and similar macnonutnient puter databases of foods Denmark of energy E.qeriitieiztal The two (Dankost) and nutrient prok)co/ test meals were and
balance on the 2 test days. The comfrom the National Food Agency of Italy (INN) were used in the calculations diets. of the test
Samples
composition
by
Englyst
the
methods
(22).
de-
Cummings
given
in a crossover
design
on
sethe at
sub-
parate days with I wk and no more test days. On the test day the subjects
0800, with having a minimum fasted for of physical the
Statistical
analyses Data are presented as by using the second Responses analysis to the of variance
activity,
or train
All results are given as means SEM. changes from basal fasting concentrations fasting two blood test meals sample were as the basal compared pained nested and the 5-h concentration. measures into diet. degrees measurement by parametric
after
jects
12 h from
voided
and
were
weighed
ance was measured. The subjects then rested in the supine position on a bed covered with an antidecubitus mattress with slight elevation of the head. A Venflon catheter (Viggo. Gothenborg. Sweden) was inserted in an antecubital arm vein. After a 10-mm rest a fasting blood sample was taken and after a further 20-mm rest nesting metabolic by using a ventilated taken
within
(ANOVA) for repeated, factors and with subject sented the with F or t values (AUCs) for curves
with time and diet as The key results are preof freedom. periods Areas were under calthe area
t test same
rate was measured by indirect hood. A second fasting blood the test
the
culated separately for each subject as the difference between integrated area of the response curve and the rectangular determined was used subject. between by the basal values ( = net response). A paired in the comparisons between two means on the Regression analyses were (referred performed to as S-R) peak/nadir to account the S and R meals
hereafter
10 mm.
and
Exactly
meal
same
was
time
then
was
served
spent
on
on the differences for the 5-h AUCs values, and peak/ for the data being
meals for each individual subject. tune was measured for 5 h (1000were taken IS, 30, 45, 60, 75, 90, and dial
energy expendi1500 h), and blood samples 105, 120, 150, 180, 210, 240,
Postprandial
and means for the VAS scores, Lnadir values. This was done paired.
ics
3(X) mm
after measurements
movies,
consumed. During the postpnanwere allowed to watch light ena break of a maximum of 5
The software
tertainment
mm
after 2 and 4 h. During the break the subjects could sit, walk quietly, or go to the toilet. The exact time schedule was noted and repeated on the following test days. Water consumption duning the test period was allowed, but the total amount consumed
Rockville, Institute,
MD) and the Statistical Analysis Cany, NC) were used in the statistical
Results
Glucose Fasting mmol/L and lactate glucose the S meal concentrations and 4.91 averaged 0.07 mmolIL 4.97 0.08 the
was
noted
and
repeated
on the second
test day.
100-mm
were visual
by each subject. Ratings were made scales (VAS) with words anchored
plasma before
before
each end, expressing the most positive (ie, good, pleasant) or the most negative ratings (ie, bad, unpleasant) (23). Immediately aften the test meals the palatability, taste, aftertaste, texture, and
visual using lished appeal VAS of the scones. two Data (A test on meals energy A were recorded by are ML the being Heijnen, subjects pubP expenditure Raben,
R meal observed
ing nine
(NS). A significant interaction between diet and after the test meals with glucose concentrations
times as much after the S meal as after the
0.29 79.53
mmol/L
=
after
25.2,
R,
15 mm)
(F1122151
separately
Tagliabue,
min/L
the R
E Pasquali,
Astrup,
unpublished
observations,
S meal
0.0015).
area with
13.37
analyses was
cannula
meal
Blood
tecubital
sampled
by
without
using iced
stasis
through
the
Plasma
indwelling
glucose
anand
mmol min/L) (t5 = 7. 1 1 , P < Plasma lactate concentrations with and tion from than a peak after 45 mm
increased
syringes.
(1 .36
mmolIL),
lactate Plasma
enzymatic tnichlonacetic
after 15 mm for the R meal ( 1 . I 8 0.10 mmol/L) (interacdiet-time: F,,215, = 25.2, P < 0.0001) (Fig I). The increase basal was twice after the R meal 10.0 as high after the S (0.52 (0.24 0.06 mmol/L). mmol min/L after after the R meal (t9 the
=
as described by Chernick (25). Blood for deplasma catecholamines was collected in tubes glycol-bis(fl-aminoethyl and glutathione. ether)-N.N.N,NSamples were imme(EGTA)
ethylene
3.70,
0.005).
RESISTANT
STARCH,
GLYCEMIA, Insulin,
SATIETY GLPI concentrations averaged and 75.4 10.0 pmolIL 53.7 before
547
Plasma
mmolL
glucose
5-hour
mmol
#{149}
AUC
#{149}
mm
E
-2.0 -1.0
0.0 1.0 2.0 3.0 4.0 5.0
Fasting plasma insulin pmol/L before the S meal meal (NS). served after trations
pmol/L
plasma
after
increased
but
of six to 355.4
7.2 pmollL
(interaction AUCs
diet-time:
F1514, after
15.14,
.
averaged I .2 nmol
.
min/L
R meal and the
the S meal
=
-6.6
0.0008).
min/L
the
4.90, (-1.4
Also,
Plasma
mmol
lactate
5-hour mmol ,
<
0.9*71
between
AUC mm L
the S (18.4
1.1 nmolmin/L) (t9 = 5.34, P = 0.0005). Plasma GIP showed the same response pattern sulin
served <
inobP
(Fig
after
I ). Thus of
the R
fasting whereas
values,
by a factor
.20! .40 R S
10 after
meal
diet-time: and
14.6,
0.0001).
The
AUC
positively
-2.0
-1.0
0.0
1.0
2.0
3.0
4.0
5.0
the S meal
whereas diet-time:
the R meal
(interaction
Plasma
pmol L
insulin
5-hour
nmol
AUC L
mm
F18.71 4.7, P = 0.0002) (Fig I ). The difference in the AUCs after the R and the S meals was nearly significant O = 2.56, P = 0.06). The AUC S-R for GLP-l was negatively correlated with GIP (r = -0.94, P 0.02) and lactate (r - -0.88, P
=
<
OMJO1
with
0.052) GIP
and (r =
S-R P
=
for 0.03).
GLP-l
negatively
correlated
the two test meals (Fig 2). both meals with a nadir after effect, were F,9151 = significantly
Thus, TG decreased 2.5 h and returned to 4.1, P < 0.001). Tricorrelated with in-
Plasma
pmolL
GIP
5-hour nm mm AUC L
baseline glyceride
sulin for L.peak/Lnadir
40
I
20
(r = 0.65, P = 0.04) and the S-R (r = 0.83, P = 0.006). A tendency to a different response pattern for plasma glycerol was found after the two test meals. Thus plasma glycerol decreased after was observed
=
the S meal to a nadir after the R meal 0.06) (Fig 2). After with different mmolIL for the
after I .5 h whereas no decrease (interaction diet-time: F15 5 h glycerol S meal after the concentrations and two by test 39.8 The meals. mmolIL AUCs
Js$j
-2.0
1 .9, P
had
by 59.3 significantly
compared
fasting
The
Plasma
pmolL it
i(
GLP-l
5-hour nm mm AUC i#{149}
AUC (r =
for glycerol was negatively P = 0.01), whereas peak correlated with peak S-R
positively P = 0.02).
0.72,
-2.0
-1.0
0.0
1.0
2.0
3.0
4.0
5.0
<
interaction
between
diet
and
F,,,5,
time:
=
F,,2,5, P
25.2,
Hours FIG
gastric
after
test
(GIP),
meal of glucose,
glucagon-like
<
plasma
diet
lactate
and
(diet effect:
time:
F,,2,5,
I . Change
inhibitory
in plasma
polypeptide
concentrations
and
lactate,
peptide-l
insulin,
(GLP-
action
starch meal 154% resistant stanch (RS)] (R) and a starch meal (0% RS) (5) in 10 healthy, normalAll data arc mean (SEM), expressed as diffe-
rcnccs
effect:
from
P
fasting
0.0001);
concentrations.
plasma glucose
Left (diet
panel
<
all (time
=
25. 1. P
sulin (diet effect: F,,.,5, = 39.9, P < and time: F,5,43, = 15.1, P < 0.0001); plasma GIP (is = 5) (diet effect: F,,.5, = 27.3, P < 0.0001 : interaction between diet and time: F,5.53, = 14.6, P < 0.0001): plasma GLP-1 (, = 5) (interaction between diet and time: F,5..,7, = 4.7, P < 0.0001 ). Right panel: areas under the curves (AUC). D < 0.05. ** < 0.01, * p < 0.001.
0.0001:
548
RABEN
ET
AL and
=
Plasma
mmol L
triglycerides
5-hour
-.--
AUC L
mean
satiety
and fullness
(r
0.65,
0.04), P
=
hunger
0.049).
(r
0.62,
0.054).
inmol mm
-s
-0.1
-2.0 -1.0 0.0 1.0 2.0 3.0 4.0 5.0 A S
Discussion
Marked hormones
served after
differences as well
the two
in
test
plasma
concentrations
of substrates
and
as in palatability
meals.
and
Overall,
satiety
the
scores
S meal
were
greatly
obsti-
mulated
plasma
hormones
concentrations
whereas no
of glucose,
or only
insulin.
and
stimulation
gastroof
Plasma
I
glycerol
5-hour inmol mm
8
intestinal
AUC L
a modest
jnolL
100
these indexes was observed Plasma glucose increased after the R meal. of the analytical This data
after the R meal. nine times more after unexpected of the two
the S meal
than
50
0
. . .
fr_:::;_2:_::ii:
6i 4
TT
1.0 2.0 3.0 4.0 5.0 R S
-2.0
1.0
0.0
after
test
meal
of triglycerides
resistant 07 mean RS) (S) starch in 10 and glycerol
ratio was
in the
be1:5
sti-
in plasma
starch starch All
g) (Table
but may
3). The
be
IRSI)
healthy,
(R)
and
connected
normalas changes
of
gastrointestinal increase
and
insulin
( SEM
) expressed
from
<=
fasting 1.9.
Left
panel
areas
(ANOVA):
between diet
curves the
all (time
and
AUC).
0(8)1);
P
=
(interaction
glucose
after
the R meal,
under
amounted to 50% of be due to the fructose of the glucose being in the splanchnic
after speak response the S compared of 30: 1
meal
via nonoxidative
increased a ratio
pathways
markedly between in insulin
Epinephriu
Ploref)iPleJ)hri?le
region
No nephnine nificantly
differences after the two response changes R meal, S meal 3). The
Also, the
values is far
( I 82/6
difference
greater
meals. Thus, no served after the 2 to 4 h after the = 0.0()64) (Fig cantly
Satiet
in plasma E concentrations were obwhereas E increased significantly from (interaction diet-time: F,5,..,, = 2.68, P differences in AUCs were not signifi-
Plasma
pg #{149} ml 40
norepinephrme
-.--
5-hour
ngminL
AUC
different scores
for E on NE.
-.&-s
2:H*/i:::,Ac>f
Significant teraction P
=
were
=
found
1.95,
and
fullness
=
(in2.30,
0.03
and Thus
-2.0
-1.0
0.0
1.0
2.0
3.0
4.0
5.0
0.012) satisfied
(Fig4).
felt R
more meal.
S meal
Plasma
showed no correlations and the blood indexes between when 5-h pg
40 2:
#{149}
epinephrine
5-hour nQ mm p<OJJJ 6
L
Simple regression analysis any of the mean satiety scores AUCs mean for
nadir
correlated
ml
AUC
used. S-R
=
nadir values were included, correlated with peak S-R whereas peak P
= -
0.03) (r
=
GIP
0.057)
S-R
and
was
with
peak
food
fullness
-0.87,
prospective
consumption
(r
0.88,
0.046).
-2.0
-1.0
0.0
1.0
2.0
3.0
4.0
5.0
:I!1
and IRSI) expressed
(time effect:
F,,,,
Evaluation
of
t/,t
test
necil
after
test
meal
of norepinephrine
(54% resistant starch
The
=
3.52.
subjects found that the S meal looked P < 0.001 ). had a more unpleasant and had a firmer texture
(t
=
appetizing
(t,
=
(t
FIG 3. Changes
nephrine after a raw
in plasma
potato
concentrations
starch meal
epi(R) noras
2.84,
P than or rebe-
and
a pregelatinized male
from fasting
P
potato subjects.
<
starch All
(0%
Plasma
RS)
(5)
in 10 healthy,
<
0.05),
-5.38,
0.0004)
mal-weight.
differences
mean between
(SEM),
epinephrine
concentrations.
F,,
=
44)
8.37.
P
=
0.00()l Right
interaction areas
diet curves
and
time:
showed
2.7.
0.0064).
panel:
under
the
(AUC).
AND 4
evaluation
SATIETY
549
would be useful
did
in glucose to explain
response
In trying in gastrointestinal
lower
this
of the test
meal
at the changes
meal
a much
R
Visual appeal (0: good. 10: bad) 5.3 5.4 7.7
S
0.7 8.1 7.2 7.0 3.4 0.5 0.8 0.7 OW
response seemed
compared
with
but
time
there
to be no effect
proximal
on distal
Taste
Aftertaste
(0: pleasant.
(0: none,
10: unpleasant)
10: much)
6.0 t).8
I. I 0.8
with the increase in these hormones and GLP- I are known to be potent (3 1 ). The
may
Texture
Palatability
(0: firm.
10: loose)
10: bad) starch meal: R (unpaired
of
meals
secretion
hormones
large
therefore
difference
explain
bethe
(0: good.
7.4
0.6
8.2
potato
0.6
starch
O.O()7.
can
be
expected insulin
the
glucosethe sigthe
in
iT i: SEM.
4
R, raw potato
differentfrom
-
S. pregelatinized
ltest,
between were
meal
meal.
2 3P
=
Significantly 0.02.
4P
df=
9):
O.OO()4.
of satiety
digestible
and
potato
also Thus,
resulted
of the starch. compared Already, scones power changes were with back
and potato
slowly starch
the rate of nonoxidative glucose carbohydrate was the only energy because
be that
an
the
increased
differences
energy
load satiating
also
due
been
concentrations, It has
to result
in an increased load
(33),
to a
h postprandially.
in satiety
previously
net energy
in the meals.
A firmer
may,
require more direct measurements of glycogen stores disposal in order to explain changes in subjective sahormones
and obesity (34,
and
studies
have
demonstrated
scones. have
35).
of carbohydrate per se ( 14). We found no signibetween the changes in plasma glucose and in scores. In a recent study from our department in a low-fiber for glucose either
between the
Gastrointestinal
satiety
previously
In the present
been
study
connected
some con-
given scores
were
found between GIP and satiety scones but not beand satiety. The correlations found indicate that
correlated
ratings
study
in fact
decrease satiety and increase hunger, which is in conthe previously suggested satiating power of GIP. In the study, The however, correlations data on GIP were must therefore only available be considered for five with
with
differences
in Lspeak
which
may
re-
present subjects.
How
I have
never been
hungry
more hungry
are
you?
I
How
cannot
satisfied
bite
do
you
feel?
-.-
eat another
5.0 I
5.0
2.5
0.0 -2.5 1
56
I am not hungry at at
I
-1
am completely
0
empty
How
Nothing
much
at all
do you
think
you
can
eat?
Totally full
How
5.0 2.5
full
do
you
feel?
_j1
A lot
0.0 -2.5
-1
Not at aM hit
I
0 1 2 3 4 5 6
after scores
(5)
test
meal starch
effect:
F,,,,,,,
after starch
data satiety
test
meal
satiety
(0% fasting RS)
resistant
All
<
starch
meal from
in 10 healthy.
normal-weight.
subjects.
P
as
differences
=
values.
F,,,.,951.
=
0.0001):
=
4.94,
between
between
=
1.95,
0.03).
Fullness
(right
bottom):
interaction
2.30.
550 some caution, and need to be confirmed of the the test meals were before and any the further
RABEN conon
ET
AL 4. Englyst HN. Cummings JH. Digestion of the polysaccharidcs of some cereal foods in the human small intestine. Am I Clin Nutr I 985:42:778-87. 5. Cummings IH. Englyst HN. Fermentation in the large intestine and the available substrates. Am I Clin Nutr 1987:45:1243-55. 6. Cummings IH. Pomare EW. Branch WI, Naylon CPE, Macfarlane GT. Short-chain fatty acids in the human large intestine. portal. hepatic 7. ules and by venous amylascs. and blood. In: Gut Marshall 1987:28:1221-7.
clusions can be made. Because the volume consuming the meals cannot have influenced However, the gelatinization
time these
spent
similar,
factors
satiating power of the two meals. of the S meal and the fact that it was in gastric emptying and fullness after Also, the different
a solid meal may have resulted in a reduction rate (36) and in increased feelings of satiety this ratings satiety found meal compared with the liquid R meal.
Fuwa H. Takaya
polymerization 1980:73-100.
T. Sugimoto
Y. Degradation
Ii, ed. New
of various
of York:
starch
granPress.
Mechanisms
saccharide
of taste, visual appeal, and texture may have influenced and fullness ratings. In fact, positive correlations were between aftertaste and satiety and fullness. et at (23) preference This partly constudy by Hill with increased in which increased (palatability) of a fullness may be
I I. 12. 9. 10.
depolymerization.
Academic
8. Englyst
nana
HN. Cummings IH. Digestion of the carbohydrates (Musa paradisiaca sapientum) in the human small Am I Clin Nutr 1986:44:42-50.
Englyst in the Mathers HN, small IC. Cummings intestine Digestion JH. of man. Digestion Am I Clin of polysaccharidcs Nutr 1987:45:423-31. polysaccharides
of baintestine. of potato
meal. However, in their study there was no effect on ratings of the meal preference (23). The effect of RS on satiety shown in the present study considered lation starch increasing cause crease with a negative also nondigestible the a high-fat, energy overall intake effect weight starch of RS with control. in the diet weight regard Replacement diet has under may ratio been to appetite pose in the shown ad libitum and perhaps
of non-starch
by non-rumi-
of digestible diet.
1991:50:161-72.
balance,
an inherited
and weight
metabolic
maintenance.
deficiency
in
low-carbohydrate
of macronutnient
IE, Burley VI.
balance?
Eur
I Clin
Nutr
power
1992:46:
of dietary
Blundell in obesity
Evaluation Iohn
tions, whereas a low-fat, high-carbohydrate to decrease spontaneous food intake and weight reductions (37-39), a replacement with RS may be undesirable Whether RS in a mixed meal in long-term has the same
diet has been shown result in unexpected of digestible starch weight regulation. effect on appetite as
T, eds. Progress
London:
14. van Amelsvoort JMM, van Stratum P. Kraal JH, Lussenburg RN, Dubbelman GP. Minor difference in postprandial responses of men between starch and sugar when replacing fat in a normal meal. Br I
Nutr 1990:63:37-51.
in the present study remains, however, to be elucidated. Moreover, it is not possible to predict the effect on 24-h appetite sensations from the present 5-h results. The RS not digested in the small intestine will at a later stage, digested and fermented by bacteria
in the production and uptake
15. Tremblay A, Lavall#{233}e N, Almeras N, Allard L, Despr#{233}s I-P. Bouchard C. Nutritional determinants of the increase in energy intake associated with a high-fat diet. Am I Clin Nutr 1991:53:11347.
16. Ponikos
preload young
17.
K, Hagamen
on men. In: subsequent Appetite Kritchevsky
of short-chain
Whether elucidated.
this
may
contribute
to increasing
satiety
S. Is fibre satiating? Effects of a high fibre food intake of normal-weight and obese
1986:7:153-62.
Burley
cade. Press,
VI. BlundeIl
JE. Action
D, Bonfleld
of dietary C.
fiber
on the JW,
satiety eds.
casDietary
Anderson
In conclusion, the intake of RS resulted in significantly postprandial plasma glucose, lactate, insulin, GIP, and responses and with digestible
correlated with
fiber. Chemistry.
1990:227-46. A. Christensen 18. Raben
physiology,
NI,
and health
Madsen and
effects.
New York:
Plenum
A. Decreased fullness
postpnandial
thermogenesis
increased
GIP
and
satiety
scores.
Differences
and
pal-
also have influenced the subjective are needed to clarify the effect of and long term. the laboratory
Bente
after a high-fiber meal compared with a low-fiber meal. Am I Clin Nutr 1994:59:1386-94. 19. FAO/WHOIUNU. Energy and protein requirements. Report of a joint FAOIWHOIUNU Expert Consultation. WHO Tech Rep Sen
1985:74. 20.
RS in a mixed
We gratefully
nicians Bente
both Lene
Inge
acutely Mellem,
Timmermann,
U
tech-
Kjas Dcnsen,
John Lind,
Mathiasen. 21
.
Deuncnberg P. van den Kooy K, Leenen R, Weststnate IA, IC. Sex and age specific prediction formulas for estimating composition from bioclectnical impedance: a cross-validation
IntlObes Englyst HN, 1991:15:17-25. Kingman SM. Cummings IH. Classification and
and Karen Klausen: the dietitians Claudia Trcntani and Caterina Mamini: and lngcr-Lise Gr#{248}nfeldt and her kitchen staff for expert technical assistance as well as Grethe Thorbek for consultive assistance.
sunement
22.
of nutritionally
important
starch
fractions.
I992:46(suppl):S33-50.
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