TY - JOUR
T1 - Mucus Gel Thickness and Turnover in the Gastrointestinal Tract of the Rat
T2 - Response to Cholinergic Stimulus and Implication for Mucoadhesion
AU - Rubinstein, Abraham
AU - Tirosh, Boaz
PY - 1994/6
Y1 - 1994/6
N2 - The thickness of the mucus gel and its turnover rate were measured in the stomach, proximal jejunum, cecum and proximal colon of the rat, using microscopy and staining techniques. The specific mucus-secretory responses to carbachol-induced cholinergic stimulus in these locations were also studied. The mucus gel was found to be the thinnest (18 ±1 microns) in the cecum, and the thickest in the stomach (39 ±14 microns). The effect of carbachol on mucus secretion was profound and dose dependent in the stomach, and less profound, although still dose dependent, in the proximal jejunum. The least responsive organs were the cecum and the proximal colon, where no effect was observed after three doses of carbachol. Mucus secretion rate was significantly higher in the jejunum (1.1 ± 0.5 µg glucose equivalent min−1 cm−2) than in the colon (0.5 ± 0.2 µg glucose equivalent min−l cm−2). Also, the proximal jejunum was more responsive to the carbachol stimulus (mucus secretion rate of 5.4 ±2.2 µg glucose equivalent min−1 cm−2 after carbachol treatment) than the colon (mucus secretion rate of 1.0 ±0.4 µg glucose equivalent min−l cm−2 after carbachol treatment). In vitro mucoadhesion studies with Polycarbophil disks were performed in the mucosal tissues of the stomach, jejunum, cecum and proximal colon of the rat with and without cholinergic (carbachol) stimulus. The adhesion force in the cecum and the colon was significantly stronger than in the stomach and proximal jejunum when the studies were performed at pH 2. Carbachol treatment did not significantly change the mucoadhesion of Polycarbophil disks. It is concluded that in the gastrointestinal tract of the rat the colon and the cecum are more suitable locations for the mucoadhesion than the stomach and the jejunum because: (1) their mucus turnover is lower, (2) their sensitivity to mucus secretory stimulus is lower, and (3) their Polycarbophil adherence properties are stronger.
AB - The thickness of the mucus gel and its turnover rate were measured in the stomach, proximal jejunum, cecum and proximal colon of the rat, using microscopy and staining techniques. The specific mucus-secretory responses to carbachol-induced cholinergic stimulus in these locations were also studied. The mucus gel was found to be the thinnest (18 ±1 microns) in the cecum, and the thickest in the stomach (39 ±14 microns). The effect of carbachol on mucus secretion was profound and dose dependent in the stomach, and less profound, although still dose dependent, in the proximal jejunum. The least responsive organs were the cecum and the proximal colon, where no effect was observed after three doses of carbachol. Mucus secretion rate was significantly higher in the jejunum (1.1 ± 0.5 µg glucose equivalent min−1 cm−2) than in the colon (0.5 ± 0.2 µg glucose equivalent min−l cm−2). Also, the proximal jejunum was more responsive to the carbachol stimulus (mucus secretion rate of 5.4 ±2.2 µg glucose equivalent min−1 cm−2 after carbachol treatment) than the colon (mucus secretion rate of 1.0 ±0.4 µg glucose equivalent min−l cm−2 after carbachol treatment). In vitro mucoadhesion studies with Polycarbophil disks were performed in the mucosal tissues of the stomach, jejunum, cecum and proximal colon of the rat with and without cholinergic (carbachol) stimulus. The adhesion force in the cecum and the colon was significantly stronger than in the stomach and proximal jejunum when the studies were performed at pH 2. Carbachol treatment did not significantly change the mucoadhesion of Polycarbophil disks. It is concluded that in the gastrointestinal tract of the rat the colon and the cecum are more suitable locations for the mucoadhesion than the stomach and the jejunum because: (1) their mucus turnover is lower, (2) their sensitivity to mucus secretory stimulus is lower, and (3) their Polycarbophil adherence properties are stronger.
KW - cholinergic stimulation
KW - gastrointestinal tract
KW - mucoadhesion
KW - mucus turnover
UR - http://www.scopus.com/inward/record.url?scp=0028366107&partnerID=8YFLogxK
U2 - 10.1023/A:1018961204325
DO - 10.1023/A:1018961204325
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C2 - 7937516
AN - SCOPUS:0028366107
SN - 0724-8741
VL - 11
SP - 794
EP - 799
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 6
ER -