Activation of submucosal but not myenteric plexus of the gastrointestinal tract accompanies reduction of food intake by camostat

2008 ◽  
Vol 150 (1-3) ◽  
pp. 73-80 ◽  
Author(s):  
Shannon J. Raboin ◽  
Joseph R. Reeve ◽  
Marvis S. Cooper ◽  
Gary M. Green ◽  
Ayman I. Sayegh
2015 ◽  
Vol 5 (1) ◽  
Author(s):  
David Grundmann ◽  
Markus Klotz ◽  
Holger Rabe ◽  
Matthias Glanemann ◽  
Karl-Herbert Schäfer

1959 ◽  
Vol 37 (12) ◽  
pp. 1475-1491 ◽  
Author(s):  
Carl Peraino ◽  
Quinton R. Rogers ◽  
Minoru Yoshida ◽  
Mou-Liang Chen ◽  
Alfred E. Harper

The effects of various dietary changes on the emptying of solids and nitrogen from the stomach and on the disappearance of nitrogen from the gastrointestinal tract of rats trained to consume a single meal daily are described. When the animals were fed 5 g of food the presence of casein in the diet caused a general deceleration of stomach-emptying and altered the shape of the stomach-emptying curve. The presence of 50% of casein in the diet did not result in an accumulation of nitrogen in the intestine much above the amount found when a protein-free diet was fed. When dextrin was the dietary carbohydrate the diet emptied from the stomach as a homogeneous mixture, whereas when sucrose was the dietary carbohydrate the casein emptied from the stomach more slowly than did the other components of the diet. Raising the dietary level of fat to 50% caused a general deceleration of emptying and abolished the above-mentioned carbohydrate effect. No delay in stomach-emptying due to the presence of casein in the diet was noted when only 1.5 g of diet was fed. As the level of food intake was raised the total quantity of nitrogen emptying from the stomach per unit time increased although a greater percentage of the amount ingested emptied from the stomach when the level of food intake was low.


Nutrients ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 2366
Author(s):  
Alba Miguéns-Gómez ◽  
Carme Grau-Bové ◽  
Marta Sierra-Cruz ◽  
Rosa Jorba-Martín ◽  
Aleidis Caro ◽  
...  

In this study we compare the interaction of three protein sources—insect, beef, and almond—with the gastrointestinal tract. We measured the enterohormone secretion ex vivo in human and pig intestine treated with in vitro digestions of these foods. Insect and beef were the most effective in inducing the secretion of CCK, while almond was the most effective in inducing PYY in pig duodenum. In the human colon, almond was also the most effective in inducing PYY, and GLP-1 levels were increased by insect and beef. The three digested proteins reduced ghrelin secretion in pig duodenum, while only insect reduced ghrelin secretion in human colon. We also found that food intake in rats increased in groups fed a raw insect pre-load and decreased when fed raw almond. In conclusion, the insect Alphitobius diaperinus modulates duodenal and colonic enterohormone release and increases food intake in rats. These effects differ from beef and almond.


Author(s):  
Francesco Cavagnini

Appetite is regulated by a complex system of central and peripheral signals that interact in order to modulate eating behavior according the individual needs, i.e. the fasting or fed condition and the general nutritional status. Peripheral regulation includes adiposity signals and satiety signals, while central control is accomplished by several effectors, including the neuropeptidergic, monoaminergic and endocannabinoid systems. Adiposity signals inform the brain of the general nutritional status of the subject as indicated by the extent of fat depots. Indeed, leptin produced by the adipose tissue and insulin, whose pancreatic secretion tends to increase with the increase of fat mass, convey to the brain an anorexigenic message. Satiety signals, including cholecystokinin (CCK), glucagon-like peptide-1 (GLP-1) and peptide YY (PYY), originate from the gastrointestinal tract during a meal and, through the vagus nerve, reach the nucleus tractus solitarius (NTS) in the caudal brainstem. From NTS afferents fibers project to the arcuate nucleus (ARC) of the hypothalamus, where satiety signals are integrated with adiposity signals and with several hypothalamic and supra-hypothalamic inputs, thus creating a complex network of neural circuits that finally elaborate the most appropriate response, in terms of eating behavior. In more detail, ARC neurons secrete a number of neuropeptides with orexigenic properties, such as neuropeptide Y (NPY) and agouti-related peptide (AGRP), or anorexigenic effects such as pro-opiomelanocortin (POMC) and cocaine- and amphetamine-regulated transcript (CART). Other brain areas involved in the control of food intake are located downstream the ARC: among these, the paraventricular nucleus (PVN), which produces anorexigenic peptides such as thyrotropin releasing hormone (TRH), corticotrophin releasing hormone (CRH) and oxytocin, the lateral hypothalamus (LHA) and perifornical area (PFA), secreting the orexigenic substances orexin-A (OXA) and melanin concentrating hormone (MCH). Recently, a great interest has developed for endogenous cannabinoids, important players in the regulation of food intake and energy metabolism. In the same context, increasing evidence is accumulating for a role played by the microbiota, the trillion of microorganism populating the human gastrointestinal tract. The complex interaction between the peripheral organs and the central nervous system has generated the concept of gut-brain axis, now incorporated into the physiology. A better understanding of the mechanisms governing the eating behavior will allow the development of drugs capable of reducing or enhancing food consumption.


1989 ◽  
Vol 256 (5) ◽  
pp. G884-G896 ◽  
Author(s):  
T. Gonda ◽  
E. E. Daniel ◽  
T. J. McDonald ◽  
J. E. Fox ◽  
B. D. Brooks ◽  
...  

The distribution of nerves containing galanin-immunoreactive (GAL-IR) material was compared to the distribution of neurons containing vasoactive intestinal polypeptide (VIP) immunoreactivity in the canine gastrointestinal tract. The actions of intra-arterially administered galanin and VIP on motility in the gastric antrum and corpus and the intestines were also studied. All sphincter muscles contained galanin- and VIP-immunoreactive nerve profiles. VIP-immunoreactive nerve profiles were present in all layers of the stomach, small intestine, and colon. GAL-IR nerve somata were common in the submucous plexus of ileum and colon and in the myenteric plexus of the terminal antrum, as were nerve processes in various layers. In the small intestine, galanin inhibited contractile responses to field stimulation of intrinsic nerves and also reduced the contractions after nerve blockade with tetrodotoxin (TTX). VIP often enhanced field-stimulated contractions at low doses but inhibited these and the contractions after TTX at higher doses. In the stomach and colon, both peptides inhibited responses to field stimulation; whether these effects were due to actions on smooth muscle was not tested. The distribution and actions of galanin in gut are consistent with the hypothesis that it acts at smooth muscle sites and possibly at prejunctional sites.


1983 ◽  
Vol 85 (4) ◽  
pp. 890-899 ◽  
Author(s):  
James Christensen ◽  
Gary A. Rick ◽  
Bryce A. Robison ◽  
Michael J. Stiles ◽  
Mark A. Wix

2007 ◽  
Vol 192 (2) ◽  
pp. 313-323 ◽  
Author(s):  
Angela S Bang ◽  
Steven G Soule ◽  
Tim G Yandle ◽  
A Mark Richards ◽  
Chris J Pemberton

Ghrelin is a 28 amino acid stomach peptide, derived from proghrelin(1–94), that stimulates GH release, appetite and adipose deposition. Recently, a peptide derived from proghrelin(53–75) – also known as obestatin – has been reported to be a physiological antagonist of ghrelin in the rat. Using four specific RIAs, we provide the first characterisation of proghrelin(1–94) peptides in human plasma, their modulation by metabolic manipulation and their distribution in mammalian tissues. ghrelin(1–28) immunoreactivity (IR) in human plasma and rat plasma/stomach consisted of major des-octanoyl and minor octanoylated forms, as determined by HPLC/RIA. Human plasma ghrelin(1–28) IR was significantly suppressed by food intake, oral glucose and 1 mg s.c. glucagon administration. ghrelin(1–28) IR and proghrelin(29–94) IR peptide distributions in the rat indicated that the stomach and gastrointestinal tract contain the highest amounts of the peptides. Human and rat plasma and rat stomach extracts contained a major IR peak of proghrelin(29–94)-like peptide as determined by HPLC/RIA, whereas no obestatin IR was observed. Human plasma proghrelin(29–94)-like IR positively correlated with ghrelin(1–28) IR, was significantly suppressed by food intake and oral glucose and shared with ghrelin(1–28) IR a negative correlation with body mass index. We found no evidence for the existence of obestatin as a unique, endogenous peptide. Rather, our data suggest that circulating and stored peptides derived from the carboxyl terminal of proghrelin (C-ghrelin) are consistent in length with proghrelin(29–94) and respond to metabolic manipulation, at least in man, in similar fashion to ghrelin(1–28).


Sign in / Sign up

Export Citation Format

Share Document