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1.
Arch Surg ; 134(10): 1079-81, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10522850

ABSTRACT

HYPOTHESIS: Treatment with anti-L-selectin monoclonal antibody will reduce venular neutrophil-endothelial rolling (flux and velocity) and adhesion associated with ischemia reperfusion injury in rat skeletal muscle. DESIGN: Prospective, randomized experimental trials. SETTING: Basic science research laboratory. MATERIALS: Male Wistar rats weighing 109 +/- 5 g (mean +/- SEM). INTERVENTIONS: Gracilis pedicle muscle flaps were elevated and microcirculation was observed by intravital microscopy. Two groups were evaluated: (1) the control group, which received 4 hours of global ischemia, and (2) the experimental group, which received 4 hours of global ischemia, plus treatment with anti-L-selectin monoclonal antibody 30 minutes before reperfusion. MAIN OUTCOME MEASURES: The number of rolling and adherent leukocytes in postcapillary venules were counted in the 2 groups at baseline and at 1 through 5, 10, 15, 20, 30, 45, and 60 minutes of reperfusion. RESULTS: Treatment with the monoclonal antibody to L-selectin significantly reduced the number of rolling leukocytes (flux) at 2 through 5, 20, 30, 45, and 60 minutes of reperfusion compared with controls (P<.05). Use of the monoclonal antibody significantly reduced the number of adherent neutrophils at 5, 10, 15, 20, 30, 45, and 60 minutes of reperfusion (P<.05). There was no significant difference in leukocyte velocity. CONCLUSION: L-Selectin plays a significant role in leukocyte rolling and adherence to venular endothelium in rat skeletal muscle ischemia reperfusion injury.


Subject(s)
L-Selectin/immunology , Muscle, Skeletal/blood supply , Neutrophils/physiology , Reperfusion Injury/immunology , Animals , Male , Random Allocation , Rats , Rats, Wistar
2.
J Prosthet Dent ; 78(1): 10-4, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9237140

ABSTRACT

PURPOSE: This study evaluated the ability of resin-bonded posts to reinforce teeth that are structurally weak in the cervical area against fracture. MATERIAL AND METHODS: Forty canine roots were endodontically treated and randomly distributed into four groups of 10. Parallel-sided preformed posts were cemented into the roots of these teeth after their crowns were removed. The cervical third of the canals were flared to simulate teeth weakened in this area as a result of caries or endodontic therapy. Three resin cements and a zine-phosphate cement, which was used as the control, were used to secure the posts into the roots. Cemented posts were loaded in an Instron testing machine with a gradually increasing force at a 60-degree angle to the long axis of the root until the root fractured. RESULTS: Roots in which the posts were cemented with Panavia were significantly more resistant to fracture than those where zinc phosphate was used (p < 0.05). Because of the inability to determine exactly the point of failure of the zinc-phosphate cement, no statistically significant difference was found when compared with the other two resin cements (ANOVA and Student-Newman-Keuls test).


Subject(s)
Dental Bonding , Post and Core Technique , Resin Cements , Tooth Root , Analysis of Variance , Boron Compounds/chemistry , Cementation , Cuspid/pathology , Dental Caries/therapy , Dental Stress Analysis/instrumentation , Dentin-Bonding Agents/chemistry , Humans , Materials Testing , Methacrylates/chemistry , Methylmethacrylates/chemistry , Phosphates/chemistry , Resin Cements/chemistry , Root Canal Therapy , Stress, Mechanical , Tooth Cervix/pathology , Tooth Fractures/physiopathology , Tooth Fractures/prevention & control , Tooth Root/pathology , Tooth Root/physiopathology , Zinc Phosphate Cement/chemistry
3.
J Surg Res ; 62(2): 255-9, 1996 May.
Article in English | MEDLINE | ID: mdl-8632648

ABSTRACT

Cholecystokinin-8 placed in the gallbladder lumen causes gallbladder contraction by a neurally mediated, tetrodotoxin-sensitive mechanism. We wished to determine whether other cholecystokinin-like peptides in the gallbladder lumen cause contraction and whether this response is inhibited by cholecystokinin-receptor antagonists. In this study, we measured gallbladder contraction induced by cholecystokinin-like peptides or by hepatic bile placed in the gallbladder lumen. Isolated gallbladders were suspended in an organ bath while luminal hormones were infused. Gallbladder contraction was measured by continuous monitoring of luminal pressure. Cholecystokinin-8, cholecystokinin-5, and gastrin-17 caused dose-related gallbladder contraction with similar potency when placed in the lumen. Each stimulated 70-80% maximal contraction at a luminal concentration of 10(-6) M. Cholecystokinin-receptor antagonists CR1409 and loxiglumide partially inhibited contraction caused by luminal cholecystokinin-8. Bile from fed animals, but not from fasted animals, stimulated gallbladder contraction to 36 +/- 4% of maximal when placed in the gallbladder lumen. We conclude that cholecystokinin and gastrin peptides in the gallbladder lumen cause contraction. This may be mediated through receptors of the cholecystokinin-B type, possibly on intrinsic nerves. Bile from fed animals also contains substances that stimulate gallbladder contraction when bile is placed in the gallbladder lumen. These findings suggest intrinsic nerves participate in the postprandial gallbladder response to cholecystokinin.


Subject(s)
Cholecystokinin/physiology , Gallbladder/innervation , Gallbladder/physiology , Gastrins/physiology , Receptors, Cholecystokinin/physiology , Sincalide/pharmacology , Animals , Bile/physiology , Female , Gastrins/pharmacology , Guinea Pigs , Hormone Antagonists/pharmacology , In Vitro Techniques , Muscle Contraction , Pentagastrin/pharmacology , Proglumide/analogs & derivatives , Proglumide/pharmacology
4.
Dig Dis Sci ; 40(9): 1982-9, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7555453

ABSTRACT

Acetylcholine may be released from gallbladder intrinsic nerves in response to cholecystokinin stimulation. This study characterized metabolites of [14C]choline produced in the gallbladder and released during incubation, with or without cholecystokinin-octapeptide. Radiolabeled [14C]choline was applied to the mucosal or muscle surface of intact guinea pig gallbladders in an organ bath. After radiolabeling, gallbladders were incubated with or without the contractile agonist cholecystokinin-octapeptide. Metabolites of [14C]choline were identified in gallbladder tissue and incubation buffers using HPLC and thin-layer chromatography. The major metabolites of [14C]choline were betaine and phosphocholine. [14C]Phosphocholine was incorporated slowly into [14C]phosphatidylcholine. [14C]Choline was released into buffers during incubation. [14C]Acetylcholine constituted less than 1% of radiolabel in the gallbladder. There was no identifiable [14C]acetylcholine released in buffers. Cholecystokinin-octapeptide did not affect choline metabolism. These studies showed that choline in the gallbladder is metabolized along pathways similar to those in the liver. Gallbladders released mostly choline, rather than acetylcholine, even during hormonally induced contraction.


Subject(s)
Acetylcholine/metabolism , Choline/metabolism , Gallbladder/metabolism , Animals , Betaine/metabolism , Carbon Radioisotopes , Female , Gallbladder/drug effects , Gallbladder/innervation , Guinea Pigs , Phosphorylcholine/metabolism , Sincalide/pharmacology , Time Factors
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