The effect of single doses of pramlintide on gastric emptying of two meals in men with IDDM

被引:89
作者
Kong, MF
Stubbs, TA
King, P
Macdonald, IA [1 ]
Lambourne, JE
Blackshaw, PE
Perkins, AC
Tattersall, RB
机构
[1] Univ Nottingham, Sch Med, Sch Biomed Sci, Nottingham NG7 2UH, England
[2] Univ Nottingham Hosp, Queens Med Ctr, Dept Diabet, Nottingham NG7 2UH, England
[3] Univ Nottingham Hosp, Dept Med Phys, Nottingham NG7 2UH, England
关键词
insulin-dependent diabetes mellitus; gastric emptying; postprandial hyperglycaemia; amylin; pramlintide;
D O I
10.1007/s001250050949
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a previous study we have shown that an intravenous infusion of pramlintide (an analogue of human amylin) delayed gastric emptying, but the dose of pramlintide was supraphysiological in relation to the amylin response to food in non-diabetic subjects. The purpose of this study was to examine the dose response relationship of subcutaneous injections of pramlintide on gastric emptying and to determine whether administration of the drug before one meal has an impact on the subsequent meal. Eleven men with insulin-dependent diabetes mellitus were studied in a double-blind, randomised, four-way crossover design. None had autonomic neuropathy. Euglycaemia was maintained overnight before the study day. At -30 min the patients self-injected their usual morning insulin and at -15 min they injected the study drug (either placebo or 30, 60 or 90 mu g pramlintide) subcutaneously. At 0 min they ate a standard meal consisting of a pancake, labelled with Tc-99m, and a milkshake containing 3-ortho-methylglucose (3-OMG). Gastric emptying images were obtained for the next 8 h. At 240 min the subjects ate a similar meal, but on this occasion the pancake was labelled with In-111. All three doses of pramlintide delayed emptying of the solid component of the first meal (p < 0.004) with no significant difference between the drug doses. There were no differences between placebo and pramlintide after the second meal. All three doses of pramlintide resulted in a prolongation in the time to peak plasma 3-OMG level (p < 0.0001) after the first meal but there was no difference after the second meal.
引用
收藏
页码:577 / 583
页数:7
相关论文
共 24 条
[1]   ISLET AMYLOID POLYPEPTIDE - DOES IT PLAY A PATHOPHYSIOLOGICAL ROLE IN THE DEVELOPMENT OF DIABETES [J].
BENNETT, WM ;
SMITH, DM ;
BLOOM, SR .
DIABETIC MEDICINE, 1994, 11 (09) :825-829
[2]   EFFECTS OF MEAL INGESTION ON PLASMA AMYLIN CONCENTRATION IN NIDDM AND NONDIABETIC HUMANS [J].
BUTLER, PC ;
CHOU, J ;
CARTER, WB ;
WANG, YN ;
BU, BH ;
CHANG, D ;
CHANG, JK ;
RIZZA, RA .
DIABETES, 1990, 39 (06) :752-756
[3]   ROLE OF THE PROXIMAL AND DISTAL STOMACH IN MIXED SOLID AND LIQUID MEAL EMPTYING [J].
COLLINS, PJ ;
HOUGHTON, LA ;
READ, NW ;
HOROWITZ, M ;
CHATTERTON, BE ;
HEDDLE, R ;
DENT, J .
GUT, 1991, 32 (06) :615-619
[4]   HYPERINSULINEMIA IMPAIRS GASTROINTESTINAL MOTILITY AND SLOWS CARBOHYDRATE-ABSORPTION [J].
ELIASSON, B ;
BJORNSSON, E ;
URBANAVICIUS, V ;
ANDERSSON, H ;
FOWELIN, J ;
ATTVALL, S ;
ABRAHAMSSON, H ;
SMITH, U .
DIABETOLOGIA, 1995, 38 (01) :79-85
[5]  
Fleiss JL, 1986, The Design and Analysis of Clinical Experiments, P263
[6]   SUGAR ABSORPTION TESTS, WITH SPECIAL REFERENCE TO 3-0-METHYL-D-GLUCOSE AND D-XYLOSE [J].
FORDTRAN, JS ;
CLODI, PH ;
INGELFINGER, FJ ;
SOERGEL, KH .
ANNALS OF INTERNAL MEDICINE, 1962, 57 (06) :883-+
[7]   HYPERGLYCEMIA SLOWS GASTRIC-EMPTYING IN TYPE-1 (INSULIN-DEPENDENT) DIABETES-MELLITUS [J].
FRASER, RJ ;
HOROWITZ, M ;
MADDOX, AF ;
HARDING, PE ;
CHATTERTON, BE ;
DENT, J .
DIABETOLOGIA, 1990, 33 (11) :675-680
[8]   VALIDITY OF THE GEOMETRIC MEAN CORRECTION IN THE QUANTIFICATION OF WHOLE BOWEL TRANSIT [J].
HARDY, JG ;
PERKINS, AC .
NUCLEAR MEDICINE COMMUNICATIONS, 1985, 6 (04) :217-224
[9]   BASAL AND STIMULATED PLASMA-LEVELS OF PANCREATIC AMYLIN INDICATE ITS CO-SECRETION WITH INSULIN IN HUMANS [J].
HARTTER, E ;
SVOBODA, T ;
LUDVIK, B ;
SCHULLER, M ;
LELL, B ;
KUENBURG, E ;
BRUNNBAUER, M ;
WOLOSZCZUK, W ;
PRAGER, R .
DIABETOLOGIA, 1991, 34 (01) :52-54
[10]  
HOCHBERG Y, 1988, BIOMETRIKA, V75, P800, DOI 10.1093/biomet/75.4.800