1912
CORRESPONDENCE
this technique similar
GASTROENTEROLOGY Vol. 107, No. 6
has advantages
over current
alternatives
that provide
information?
the smooth
muscle
significantly
lower quantities
sphincters
cent nonsphincteric
E. E. DANIEL
The studies
Department of Biomedical Sciences
comparing
Faculty of Health Sciences
motility
We appreciate
SUSHANTA
tinal polypeptide gene expression is characteristically higher in opossum gastrointestinal sphincters. Gastroenterology 1994; 106:1467-1476.
Reply.
The issue raised by Dr. Daniel
studies
using
important study
molecular
to keep in mind
of VIP mRNA
the neuropeptide bodies.
biology
transcripts,
but
disorders
are transported
try usually
requires
nocytochemical reason
studies
there
tent.
RIA
will
in these
simply
content
without
any relationship
problem
of antibody
The present
recognition
studies
muscle sphincteric importance concerns
would
to the tissue
definitely
The main message transcripts
apply
VIP mRNA
transcripts
it is clear (Figure the myenteric
the differences
to minimize
the
approaches.
The
out
The Vagus, Motilin, Motor Complex Dear Sir: In a recent paper, Yamamoto cation
at pH
the intact
1 inhibits
dog stomach
not in the extrinsically
by Dr.
the VIP mRNA
reflex whereby
denervated
fibers would neurons
vagal efferent
inhibit
We would like to suggest
We would
sensory
arising
information
continued
bowel migrating
tissues.
To pinpoint
the
ance ofphase
to compare
the
is, with
muscle
is coming
cells, suggesting
transcripts
in smooth
from
may not be ex-
muscle
mass of two
differences
in VIP
cycling
III-like
gastric
activity
acidification,
with vagal blockade small
bowel
efferent ticularly
phase
(absent
vagal pathways
cells of Cajal,
excitation)
ance of gastric Cal3 and/or
in sphincteric actin
vs. nonsphincteric
tis-
is a novel idea but may not be
our recent
studies2
increases
acidification,
types of cells is not known. muscle
blockade
have shown
that
of inhibitory
more
tonic,
probably
into play with chronic Whether inhibition
in response
to mot&n is identical
acidification
reflects
injections.2
That shown
phase III with persistence
of the
blockade
neither
afferent
Thus, vagal integrity whether other
responds
such
is cycli-
as a cyclical
this activity.4X’ The fact to the motilin
and is not influenced the adaptive
nor
(and par-
for the normal appearthis excitation
factors
levels to produce pouch
the small the appear-
to that
vagal
allowing
to
phase III activity
the picture
activity
of vagal input,
is primarily
of the vagal nerves
levels with
appears to be a prerequisite
phase III-like
that in our view
gastric
mot&n
are operative.
in the absence
of interstitial
activation
(MMC) but also prevents
gastric
III). With
the differences.
the contribution
to the low pH
acidification
Cooling
motor complex
gastric
Interestingly,
from gastric
of plasma
types of cells. From our studies’
propose
that the effect of the vagal
the spontaneous
that the message
in but
these vagal efferent
explanation
propose
turn off vagal efferent excitation.
motilin
sues based on smooth
through
an alternate
is even more likely.
in plasma
always practical.
fibers responding
the stomach
pouch
is a long vagovagal
fibers. Presumably
in dogs not only abolishes
than
gastric
pouch.’ The authors
despite
there were no apparent
the VIP content
gastric
acidifi-
activity
in the stomach.
that the denervated
To compare
innervated
vs. nonsphincteric)
in all the sphincteric
III-like
for this inhibition
vagal sensory afferent
in turn activate
phase
and the vagally
mRNA levels in the tissues with or without mucosa, suggesting a minimal contribution of submucosal neurons and the mucosa toward blood vessels, and other
et al. showed that intragastric
motilin-induced
show that the levels
in the VIP mRNA
However,
and the Migrating
(sphincteric
and not the smooth
Likewise,
Street
The studies muscle
in different
Waht
1025
Philadelphia, Pennsylvania 19107
it will be important
smooth
on the basis of the differences
types of tissues.
they
tract for VIP mRNA
as pointed
higher
6 in our paper)
neurons
Thomas Jeffwson University
that the most likely explanation
levels.
to RIA and immunocytochemistry.
were reproducibly
nonsphincteric
of the neuro-
new because
was never
composition
of tissues
basis for the differences,
in the tissues
to scan all smooth
of the study’ was to compare
in two types
the adjacent
that
and
investigations
the
origin
Then there is a
and breakdown
important
of the tissue composition.
of VIP mRNA
plained
neurons.
in the neuropeptide
of the study
con-
without
extrinsic
of the RIA and immunocytochemistry related
regardless
of the peptide
regions of the gastrointestinal
The purpose
immunocyto-
by the VIP variants
are both
for this
of the peptide
of unknown
These limitations
results.
VIP RIA may include
to the intramural
the first comprehensive
expression.
cellular
Therefore,
may lead to wide variations
constitute
In addition,
the presence
M.D.
D.V.M.
tinal polypeptide gene expression is characteristically higher in opossum gastrointestinal sphincters. Gastroenterology 1994; 106:1467-1476. 2. Liddell RA, Chakder S, Rattan S, McHugh K. Differential isoactin gene expression in the sphincteric and nonsphincteric gastrointestinal smooth muscles of the opossum. Proc Sot Exp Biol Med 1994;205:321-326.
the
for immu-
Perhaps
PH.D. PH.D.
on the neuropeptide
quantitation
of the nerve terminals
investigation.
peptide
Daniel
show
variable
difficult
thickness.
regions.
provide
the site of its origin.
peptide
under
of their
lack of information
does not readily
revealing
with
and
addressed.
1. Bandyopadhyay A, Chakder S, Lynn RB, Rattan S. Vasoactive intes-
the synthesis,
are notoriously
because
is a relative
immunocytochemistry chemistry
pretreatment,
VIP neuro-
cell
down the axon to the nerve terminal.
regions
affecting
raised by Dr. Daniel
are im-
of the cell bodies, immunocytochemis-
colchicine
the sphincteric
for
tissues in the
Division of Gastroenterologyand Hepatolog3i
is to be able to examine
Following
B. LYNN,
groundwork
Department of Medicine
In the
level in the neuronal
limitations.
for the visualization
Moreover,
the merit
RICHARD
It is
(RIA) and immunocytochemistry
have certain
neuropeptides Therefore,
approaches.
CHAKDER,
SATISH RATTAN,
to most of the
newer
of each approach.
at the transcriptional
Radioimmunoassay
portant
is applicable
and other
the strengths
important
the questions
ALOK BANDYOPADHYAY,
1. Bandyopadhyay A, Chakder S, Lynn RB, Rattan S. Vasoactive intes-
express
than the adja-
gastrointestinal
hope that these have been appropriately
Hamibon, Ontario, Canada L8N 325
tract
mRNA
tissues.
provide
in different
of certain
transmission.
1200 Main Street West
muscle
above
the VIP mRNA
pathophysiology
McMaster University
smooth
discussed
of the gastrointestinal of total isoactin
injection
by the gastric
mechanisms
that
come
denervation.* of the stomach
of the stomach
through
can induce
sympathetic
active adrenergic pathways
was not
December 1994
studied
CORRESPONDENCE
in the paper
is mentioned
by Yamamoto
in the abstract
is also less likely.
With
et al., although
summary.
and motilin
injections
in the presence
vagal blockade,
absence
personal
do not produce
of pharmacological
this possibility
We suspect
phase III of the MMC is not due to unopposed
this mechanism
phase
Dear Sir:
of the spontaneous
adrenergic
adrenergic
Lieverse et al. report that in human
inhibition6
III-like
activity
blockade
(unpublished
even
3.
4.
5.
6.
of cholecystokinin plasma ings,
observations).
of Phase III activity by acidifying stomach in vagally denervated and innervated dogs with gastric pouches. Gastroenterology 1994; 106:1533-1541. Hall KE, Greenberg GR, El-Sharkawy TY, Diamant NE. Relationship between porcine motilin-induced migrating motor complex-like activity, vagal integrity, and endogenoug motilin release in dogs. Gastroenterology 1984;87:76-85. Miolan JP, Roman C. Discharge of efferent vagal fibers supplying gastric antrum: indirect study by nerve suture technique. Am J Physiol 1978;235:E366-E373. Andrews PLR, Bingham S. Adaptation of the mechanisms controlling gastric motility following chronic vagotomy in the ferret. Exp Physiol 1990:75:811-825. Grundy D, Hutson D, Scratcherd T. A permissive role for the vagus nerves in the genesis of antrc-antral reflexes in the anaesthetized ferret. J Physiol 1986;381:377-384. Chung SA, Valdez DT, Diamant NE. Adrenergic blockade does not restore the canine gastric migrating motor complex during vagal blockade. Gastroenterology 1992; 103:1491-1497.
concentrations,
dance
with
conclusions
McLaughlin Pavihon
Toronto, Ontario MST 2S8, Camah
very much the comments
et al., and we basically
agree with
that the effect of the vagal sensory acidification paper,
is primarily
however,
the stomach
the mechanism stomach
activation
by which
through
the present from gastric
study
elucidated
from gastric
that
the vagally indicate
neurons
induces
phase
in the stomach.
decreases
feeding
decrease
Furthermore,
in food intake
is in accor-
The results
to those of their with
saline infusion.
subjective
criteria
such as desire to eat, hunger
fullness, and prospective
feeding
intentions
Lieverse
et al. conclude
in this former
CCK-33
to plasma
meal does not have a major hunger recent
feelings.” paper
unclear
They
“.
effect on food intake findings
infusion
of
after a fatty
and postprandial
in the discussion
of their
and conclusions
which
are
to us.
Our own studies
support
a role for endogenous
satiety.3 We have also given a CCK-8 dial plasma intake
that
to those observed
do not comment
on these different
feelings,
were not affected by CCK.
study
levels comparable
and
previous
did not produce
CCK-33
compared
feel-
compared
thar “This finding
work in which the same dose of intravenous a significant
in hunger
intentions
effect of CCK.”
are in contrast
infusion
physiological
concentrations
compared
infusion
CCK in control
to reproduce
and shown a significant
of
postpran-
reduction
in food
with saline infusion4
A. B. BALLINGER M. L. CLARK
cholinergic
that activation
pathway. of sensory
that
similar
and that this problem
of motilin’s
action
action
in the is finally
Our findings neurons
in
arising
to turn off the vagal efferent excita-
on the pathway
are identical
us.
that includes
the mechanism
findings,
cannot
the vagova-
by which
antral
be substantially
only because
Lieverse RJ, Jansen JBMJ, Masclee AM, Lamers CBHW. Satiety effects of cholecystokinin in humans. Gastroenterology 1994; 106:1451-1454. Lieverse RJ, Jansen JBMJ, Zwan A vd, Samson L, Masclee AAM, Lamers CBHW. Effects of a physiological dose of cholecystokinin on food intake and postprandial satiation in man. Regul Pept 1993; 43:83-89. Ballinger AB, Clark ML. L-Phenylalanine releases cholecystokinin and is associated with reduced food intake in humans: Evidence for a physiological role of CCK in control of eating. Metabolism 1994;43:735-738. Ballinger AB, McLaughlin L, Medbak S, Clark ML. Cholecystokinin is a satiety hormone at physiological postprandial concentrations. Gut 1993; 34:AlOl.
the pictures
is closely related to the mechanism
Reply.
The regulation
of appetite
control
is complex.
in animals,
regulation
Like Drs. Ballinger
and Clark, we are interested
in the regulation
of food
in humans.
in the role of CCK The recent allowing
development
measurement
and the availability
We have studied plasma
in fasting
subjects,’
Gastrointestinal Research Laboratory
CCK on satiety
Gunma University
decreases
Maebashi, Japan
intentions
CCK-receptor
control
antagonists
delineating
in humans.
subjects.i
of CCK that produced
satiety
we have studied
feelings,
have enabled
the physiological
on preprandial
and on postprandial
after stimulation
in fasting
its
in both lean and obese subjects.
concentrations
in this journal,
in hunger
intake
about
and specific radioimmunoassays
the effect of an infusion
meal.’ In addition
As reported
is known
of the low plasma CCK levels in human plasma of potent
role of CCK in appetite
a preload
of sensitive
a series of experiments
us to perform
physiological
and very little
Most studies
have been performed
0. YAMAMOTO 2. ITOH Institute of Endominology
7BE, England
At present,
III activity
that motilin’s
blocks phase III in the stomach by comparing
In our
fibers inhibit
draw such a conclusion.
appears
We believe
excitation.
these vagal
of inhibitory
motilin
somewhere
gal reflex center. acidification
arising
but it is certain
acidification
tion by motilin
explanation
information
et al. seem to have misunderstood
we cannot
is not known,
mediated
alternate
to turn off vagal efferent
Drs. Diamant
From our experiment
made by Drs. Dia-
their
we did not propose
through
In this respect,
satiety
of this study
London EClA
3 99 Bathurst Street
We appreciate
significant
They conclude
a physiological
produced
Department of Gastroenterology
Toronto Hospital (Wartern Division)
Reply.
induced
an intravenous
which
St. Bartbo/omew’s Hospital
Gastrointestinal Motility Research Laboratory
mant
subjects
(CCK-33),
the wish to eat, and prospective
N. E. DIAMANT S. A. CHUNG K. E. HALL
12-419
33
with saline infusion.’
1. Yamamoto 0, Matsunaga Y, Haga N, Mizumoto A, ltoh Z. Inhibition
2.
1913
with
satiety parameters without,*
intraduodenal
the infusion
and with
the effect of endogenous fat.*
of CCK induced
significant
the wish to eat, and prospective No clear differences
between
feeding lean an