Cefaclor, a cephalosporin antibiotic, delays gastric emptying rate by a CCK-A receptor-mediated mechanism in the rat

التفاصيل البيبلوغرافية
العنوان: Cefaclor, a cephalosporin antibiotic, delays gastric emptying rate by a CCK-A receptor-mediated mechanism in the rat
المساهمون: Bozkurt, A, Deniz, M, Yegen, BC
بيانات النشر: NATURE PUBLISHING GROUP
سنة النشر: 2000
مصطلحات موضوعية: cephalosporins, gastric emptying, cholecystokinin (CCK), CCK-A receptors, capsaicin, STIMULATE CHOLECYSTOKININ SECRETION, PANCREATIC ENZYME SECRETION, TRYPSIN-INHIBITOR, DIABETIC GASTROPARESIS, FEEDBACK-REGULATION, SENSORY NEURONS, MONITOR PEPTIDE, BINDING-SITES, STC-1 CELLS, ERYTHROMYCIN
الوصف: 1 Studies in vitro suggest that cephalosporin antibiotics release the gut hormone cholecystokinin. Cholecystokinin is known to inhibit gastric emptying. Here we examine the effects of cefaclor on gastric emptying and intestinal motility. 2 Male Sprague-Dawley rats were fitted with gastric cannulas. Following a 3-week recovery, the rate of gastric emptying of saline, peptone (4.5%) or cefaclor was determined after instillation into the gastric cannula, while intestinal transit was measured by using the propagation of arabic gum + charcoal mixture given intraduodenally. 3 Gastric emptying of saline was significantly delayed by the addition of cefaclor (3, 10, 30 or 100 mM). The CCK-A antagonist SR-27897B (1 mg kg(-1), i.p.) reversed the delay induced by 10 mM cefaclor, whereas the CCK-B antagonist CI-988 (1 mg kg(-1), i.p.) had no significant effect. In capsaicin-treated rats, 10 mM cefaclor emptied more rapidly than in vehicle-treated animals. 4 Thirty-minute intestinal transit was increased at 30 and 100 mM of cefaclor, while the gastric acid secretion following cefaclor instillation was no different than the group which received saline. 5 The cephalosporin antibiotic cefaclor appears to be a potent stimulant of CCK release from gut endocrine cells, resembling the effects of peptone. Cefaclor delays gastric emptying via capsaicin-sensitive afferent pathways, which involve CCK-A receptor interaction.
نوع الوثيقة: conference object
اللغة: English
تدمد: 0007-1188
العلاقة: BRITISH JOURNAL OF PHARMACOLOGY; https://hdl.handle.net/11424/263565Test; WOS:000089716100003
DOI: 10.1038/sj.bjp.0703585
الإتاحة: https://doi.org/10.1038/sj.bjp.0703585Test
https://hdl.handle.net/11424/263565Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.DE6B8449
قاعدة البيانات: BASE
الوصف
تدمد:00071188
DOI:10.1038/sj.bjp.0703585