Duplex ultrasound measurement of changes in mesenteric flow velocity with pharmacologic and physiologic alteration of intestinal blood flow in man. 1989

M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
Department of Surgery, Northwestern University Medical School, Chicago, IL 60611.

Duplex ultrasound scanning has been used to assess mesenteric blood flow in normal and disease states. To investigate this technique we studied nine normal volunteers at rest and under conditions known to modify intestinal blood flow. After a baseline mesenteric duplex scan, each subject was given one of three treatments in random order: (1) test meal (710 kcal), (2) intravenous glucagon (40 micrograms/min), or (3) intravenous vasopressin (0.2 units/min). Peak systolic and diastolic velocities and vessel diameters were measured at intervals after treatment in the celiac and the superior mesenteric arteries (SMAs) and the right common carotid artery. Resting velocities did not differ among the groups. Peak systolic velocity increased significantly in both celiac and SMAs after the meal, with maximal changes in the celiac artery preceding those in the SMA in most subjects. Early diastolic flow reversal in the SMA was consistently lost after the meal (eight of nine subjects). Velocity changes after glucagon closely paralleled those after the meal. Vasopressin produced significant decreases in peak systolic velocity in both visceral vessels. No changes in vessel diameter were noted after any treatment. Coefficient of variation for repeated measures of peak velocities was 19% in the celiac and 12% to 16% in the SMA and the common carotid. The coefficient of variation for repeated measurements of arterial diameter was 6% to 8% in the SMA and 11% in the celiac artery. Clinically relevant changes in mesenteric hemodynamics can be reproducibly detected and quantitated by means of current duplex ultrasound technology. The similarities between the visceral arterial responses to a meal and glucagon are of interest.(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D007422 Intestines The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE. Intestine
D008297 Male Males
D008638 Mesenteric Arteries Arteries which arise from the abdominal aorta and distribute to most of the intestines. Arteries, Mesenteric,Artery, Mesenteric,Mesenteric Artery
D012039 Regional Blood Flow The flow of BLOOD through or around an organ or region of the body. Blood Flow, Regional,Blood Flows, Regional,Flow, Regional Blood,Flows, Regional Blood,Regional Blood Flows
D001783 Blood Flow Velocity A value equal to the total volume flow divided by the cross-sectional area of the vascular bed. Blood Flow Velocities,Flow Velocities, Blood,Flow Velocity, Blood,Velocities, Blood Flow,Velocity, Blood Flow
D002339 Carotid Arteries Either of the two principal arteries on both sides of the neck that supply blood to the head and neck; each divides into two branches, the internal carotid artery and the external carotid artery. Arteries, Carotid,Artery, Carotid,Carotid Artery
D002445 Celiac Artery The arterial trunk that arises from the abdominal aorta and after a short course divides into the left gastric, common hepatic and splenic arteries. Arteries, Celiac,Artery, Celiac,Celiac Arteries
D004435 Eating The consumption of edible substances. Dietary Intake,Feed Intake,Food Intake,Macronutrient Intake,Micronutrient Intake,Nutrient Intake,Nutritional Intake,Ingestion,Dietary Intakes,Feed Intakes,Intake, Dietary,Intake, Feed,Intake, Food,Intake, Macronutrient,Intake, Micronutrient,Intake, Nutrient,Intake, Nutritional,Macronutrient Intakes,Micronutrient Intakes,Nutrient Intakes,Nutritional Intakes
D005260 Female Females
D005934 Glucagon A 29-amino acid pancreatic peptide derived from proglucagon which is also the precursor of intestinal GLUCAGON-LIKE PEPTIDES. Glucagon is secreted by PANCREATIC ALPHA CELLS and plays an important role in regulation of BLOOD GLUCOSE concentration, ketone metabolism, and several other biochemical and physiological processes. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p1511) Glucagon (1-29),Glukagon,HG-Factor,Hyperglycemic-Glycogenolytic Factor,Proglucagon (33-61),HG Factor,Hyperglycemic Glycogenolytic Factor

Related Publications

M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
December 1991, Ultraschall in der Medizin (Stuttgart, Germany : 1980),
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
March 1986, Journal of vascular surgery,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
January 1986, Gut,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
November 1988, Gastroenterology,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
September 1993, Pediatric research,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
January 1985, Advances in cardiology,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
February 2001, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
September 1988, European journal of obstetrics, gynecology, and reproductive biology,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
July 2001, Journal of neuroimaging : official journal of the American Society of Neuroimaging,
M P Lilly, and T R Harward, and W R Flinn, and D R Blackburn, and P M Astleford, and J S Yao
August 1951, The Journal of physiology,
Copied contents to your clipboard!