AJCN 19th International Congress of Nutrition
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q
Agricola
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q
American Journal of Clinical Nutrition, Vol. 76, No. 6, 1302-1307, December 2002
© 2002 American Society for Clinical Nutrition

Original Research Communication

The metabolic response to ingested glycine1,2,3

Mary C Gannon, Jennifer A Nuttall and Frank Q Nuttall

1 From the Metabolic Research Laboratory and the Section of Endocrinology, Metabolism, and Nutrition, Minneapolis VA Medical Center (MCG, JAN, and FQN), and the Departments of Medicine (MCG and FQN) and Food Science and Nutrition (MCG), University of Minnesota, Minneapolis.

2 Supported in part by a grant from the Minnesota Medical Foundation, by funds from the Minnesota Obesity Center, and by Merit Review funds from the Medical Research Service, Department of Veterans Affairs. Glycine was a gift from Terry Masai and the Ajinomoto Company.

3 Address reprint requests to MC Gannon, Metabolic Research Laboratory, VA Medical Center (111G), Minneapolis, MN 55417. E-mail: ganno004{at}tc.umn.edu.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Background: The metabolic effects of dietary protein are complex. In persons with type 2 diabetes, protein ingestion results in little or no increase in plasma glucose concentrations but a stimulation of insulin and glucagon secretion. Furthermore, when protein is ingested with glucose, a synergistic effect on insulin secretion is observed. The most potent protein is gelatin, which consists of 30% glycine residues.

Objective: The objective of the present study was to determine whether glycine per se stimulates insulin secretion or reduces the glucose response when ingested with glucose.

Design: Nine healthy subjects were tested on 4 separate occasions. Plasma glucose, insulin, glucagon, and glycine concentrations were measured at various times during a 2-h period after the ingestion of 1 mmol glycine/kg lean body mass, 25 g glucose, 1 mmol glycine/kg lean body mass + 25 g glucose, or water only, given in random order.

Results: Plasma concentrations of glycine and glucagon were elevated after the ingestion of glycine, as expected. The serum insulin concentration also was slightly elevated after the ingestion of glycine alone. When glycine was ingested with glucose, the plasma glucose area response was attenuated by > 50% compared with the response after the ingestion of glucose alone. The dynamics of the insulin response after the ingestion of glycine plus glucose were modestly different from those after the ingestion of glucose alone, but the area response was not significantly different.

Conclusion: The data are compatible with the hypothesis that oral glycine stimulates the secretion of a gut hormone that potentiates the effect of insulin on glucose removal from the circulation.

Key Words: Glycine • insulin • glucose • glucagon • gut hormones • incretin • amino acids


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Our laboratory is interested in the metabolic response to ingested proteins, particularly in persons with type 2 diabetes. The reason for this interest is that ingested protein either results in no increase in peripheral blood glucose concentrations or increases them only modestly (1, 2). However, ingested protein stimulates both insulin and glucagon secretion. In addition, in persons with type 2 diabetes, protein ingested with glucose reduces the integrated, single-meal glucose area response when compared with that after the ingestion of only glucose by the same subjects. This is due to a synergistic stimulation of insulin secretion when protein is ingested simultaneously with glucose (3).

Of 7 different protein sources tested previously, one of the most potent was gelatin (4). This was somewhat surprising because gelatin is an atypical protein. On a molar basis, glycine makes up {approx}30% of the total amino acids present (5). Therefore, we were interested in determining whether glycine itself stimulates insulin secretion or reduces the integrated glucose response when ingested with a standardized amount of glucose. We first determined the response in normal young subjects.


   SUBJECTS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Nine healthy subjects were studied (4 women, 5 men). The subjects’ ages ranged from 21 to 52 y. Their mean body mass was 75 kg (range: 58.5–88.7), and their mean lean body mass was 61 kg (range: 48–72 kg). The subjects’ mean body mass index (in kg/m2) was 25.9 ± 0.5 (range: 24.1–28.2). The results of thyroid, renal, and liver function tests were normal. The subjects were nondiabetic on the basis of the National Diabetes Data Group criteria, which were in effect at the time this study was begun (6). At that time, a fasting glucose concentration on more than one occasion of >= 7.8 mmol/L (140 mg/dL) for venous plasma or >= 6.7 mmol/L (120 mg/dL) for venous whole blood or capillary whole blood was considered compatible with a diagnosis of diabetes. Written informed consent was obtained from all subjects, and the study was approved by the Department of Veterans Affairs Medical Center and the University of Minnesota Committees on Human Subjects.

The subjects were studied in the Special Diagnostic and Treatment Unit after they had fasted for 12 h overnight. An indwelling catheter was placed into a forearm vein and flushed with 0.9% saline. Baseline blood samples were obtained at 0730, 0740, and 0750. At 0800 the subjects ingested in random order on separate occasions 1–14 d apart 1 mmol glycine/kg lean body mass, 1 mmol glycine/kg lean body mass + 25 g glucose, 25 g glucose, or water only. Blood was obtained at 10-min intervals over the subsequent 2-h period. Plasma or serum was assayed for glucose, insulin, glucagon, and amino acids, including glycine.

The plasma glucose concentration was measured by a glucose oxidase method with the use of a Beckman glucose analyzer with an oxygen electrode (Beckman Instruments, Fullerton, CA). Serum immunoreactive insulin was measured by a standard double-antibody radioimmunoassay method with kits produced by Endotech (Louisville). Glucagon was measured by radioimmunoassay with 30K antiserum purchased from Health Science Center (Dallas). Individual amino acids were measured by HPLC in the laboratory of KS Nair (Rochester, MN). Lean body mass was determined by bioelectrical impedance analysis (with an instrument from RJL Systems, Clinton Town, MI).

The areas under the curves were calculated by using the trapezoidal rule (7). The initial fasting value of the respective hormone or metabolite was used as a baseline, and the area was measured over the 2-h period after the ingestion of the test substance. Statistics were determined by repeated-measures analysis of variance (ANOVA) with the MINITAB computer program (version 10.5; Minitab, Inc, State College, PA), followed by post hoc matched, paired t tests, which were Bonferroni-corrected for multiple comparisons. Data are presented as means ± SEMs.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Glycine concentration
The mean amount of glycine given was 4.6 g (range: 3.6–5.4 g). The mean fasting glycine concentration for all studies was 220 ± 22 µmol/L (range: 205–236 µmol/L; Figure 1, topGo). After the ingestion of water or glucose only, the plasma glycine concentration remained constant. After the ingestion of glycine, the plasma glycine concentration increased from a baseline of 217 ± 21 µmol/L to a peak of 909 ± 106 µmol/L at 40 min, after which it decreased toward the fasting baseline. At the end of the study, however, the plasma glycine concentration was still elevated (414 µmol/L). When glucose was ingested with glycine, the response was attenuated and modestly prolonged compared with that after glycine ingestion alone. The area response to glycine + glucose was slightly but not significantly less than that after the ingestion of glycine alone (Figure 1, bottomGo).



View larger version (25K):
[in this window]
[in a new window]
  		FIGURE 1. . Top: Mean (± SEM) plasma glycine response in 9 healthy subjects after the ingestion of water only ({circ}....{circ}), 25 g glucose (•––•), 1 mmol glycine/kg lean body mass ({triangleup}– –{triangleup}), or 25 g glucose + 1 mmol glycine/kg lean body mass ({blacktriangleup}——{blacktriangleup}). Bottom: The 120-min net integrated glycine area response with the use of the concentration at time zero as baseline. n = 9. Bars with different letters are significantly different, P <= 0.01.

 
Other amino acid concentrations
Data for the other amino acids that yielded a significant area response are presented in Table 1Go. The net alanine, glutamine, and serine area responses after the ingestion of glycine were significantly greater than after the ingestion of water only. Plasma arginine, glutamate, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tyrosine, and valine were also measured but did not change significantly (data not shown).


View this table:
[in this window]
[in a new window]
  		TABLE 1 . Plasma amino acid concentrations1
 
Glucose concentration
The mean fasting plasma glucose concentration was 4.3 ± 0.17 mmol/L (77 ± 3 mg/dL) (Figure 2, topGo). After the ingestion of water only, the plasma glucose concentration remained stable. After the ingestion of glycine, the glucose concentration also was stable. The glucose concentration after glucose ingestion increased, reached a maximum of 6.9 mmol/L (124 mg/dL) at 30 min, and returned to baseline at 70 min. When glycine was ingested with glucose, the rise in the plasma glucose concentration was attenuated by {approx}15%. The plasma glucose concentration then rapidly decreased to below the fasting baseline at 70 min. By 100 min, the glucose concentration was not significantly different whether or not glycine was ingested with glucose. The 2-h integrated glucose area response to glycine + glucose was < 50% of the response to glucose alone (Figure 2, bottomGo).



View larger version (27K):
[in this window]
[in a new window]
  		FIGURE 2. . Top: Mean (± SEM) plasma glucose response in 9 healthy subjects after the ingestion of water only ({circ}....{circ}), 25 g glucose (•––•), 1 mmol glycine/kg lean body mass ({triangleup}– –{triangleup}), or 25 g glucose + 1 mmol glycine/kg lean body mass ({blacktriangleup}——{blacktriangleup}). Bottom: The 120-min net integrated glucose area response with the use of the concentration at time zero as baseline. n = 9. Bars with different letters are significantly different, P <= 0.01.

 
Insulin concentration
The mean fasting serum insulin concentration was 48 ± 6 pmol/L (8.1 ± 1 µU/mL) (Figure 3, topGo). Glycine ingestion stimulated a modest increase in insulin concentration. After glucose ingestion, there was a rapid rise in insulin concentration, which corresponded with the rise in glucose concentration. When glycine was ingested with glucose, the insulin peak occurred later and was slightly less than when glucose was ingested alone.



View larger version (31K):
[in this window]
[in a new window]
  		FIGURE 3. . Top: Mean (± SEM) serum insulin response in 9 healthy subjects after the ingestion of water only ({circ}....{circ}), 25 g glucose (•––•), 1 mmol glycine/kg lean body mass ({triangleup}– –{triangleup}), or 25 g glucose + 1 mmol glycine/kg lean body mass ({blacktriangleup}——{blacktriangleup}). Bottom: The 120-min net integrated insulin area response with the use of the concentration at time zero as baseline. n = 9. Bars with different letters are significantly different, P <= 0.01.

 
The mean insulin area response to glycine alone was greater than that for the ingestion of water and this difference was highly significant (P < 0.01). The mean insulin area response to glycine + glucose was not significantly different from the response to glucose alone (Figure 3, bottomGo). This was despite the fact that the glucose area response was much less after glycine plus glucose ingestion.

Glucagon concentration
Glycine strongly stimulated an increase in glucagon concentration when ingested alone, and this increase persisted for the duration of the study (Figure 4, topGo). After the ingestion of water alone, glucose alone, or glycine plus glucose, the glucagon concentration decreased modestly; the decrease was greatest after glucose ingestion.



View larger version (30K):
[in this window]
[in a new window]
  		FIGURE 4. . Top: Mean (± SEM) plasma glucagon response in 9 healthy subjects after the ingestion of water only ({circ}....{circ}), 25 g glucose (•––•), 1 mmol glycine/kg lean body mass ({triangleup}– –{triangleup}), or 25 g glucose + 1 mmol glycine/kg lean body mass ({blacktriangleup}——{blacktriangleup}). Bottom: The 120-min net integrated glucagon area response with the use of the concentration at time zero as baseline. n = 9. Bars with different letters are significantly different, P <= 0.01.

 
The glucagon area increase in response to the ingestion of glycine alone was significantly different from that resulting from the ingestion of water, glucose, or the combination of glycine + glucose, as expected (Figure 4, bottomGo). None of the last 3 were significantly different from each other.


   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
Glycine is the smallest amino acid. It is readily synthesized from serine, which also can be synthesized endogenously. Thus, neither glycine nor serine is a nutritionally required amino acid. Glycine is utilized in the synthesis of several biologically important compounds, including glucose. It also is utilized in detoxification reactions and itself is a neurotransmitter.

Glycine is present in nearly all proteins, and its presence in an amino acid chain allows for an acute angulation of the chain during the folding process. This often is required for the assumption of the proper three-dimensional structure required for that protein to fulfill its functional role (8, 9).

The concentration of glycine is particularly high in structural collagen, in which 1 of every 3–4 amino acids is glycine. When these structural proteins are subjected to alkaline or acid hydrolysis and heated, they denature and form gelatin, an ingredient commonly used in foods. As indicated in the Introduction, gelatin, when ingested with glucose, strongly potentiates the glucose-stimulated increase in insulin in persons with type 2 diabetes (4).

Some individual amino acids, when given intravenously in large amounts, are known to be insulin secretagogues. The most potent of these has been reported to be arginine (10). However, a mixture of 10 nutritionally required or provisionally nutritionally required amino acids was most potent in stimulating insulin secretion. Nonnutritionally required amino acids have not been systematically studied in this regard, but are generally considered to have no effect on insulin secretion (11). Much less is known about the ability of ingested single amino acids, whether nutritionally required or not, to stimulate insulin secretion. This is particularly the case when they are ingested in amounts likely to be present in a meal.

We have begun a systematic study of the metabolic effects of individual amino acids ingested in amounts likely to be present in a high-protein meal. We initiated these studies by studying the response to arginine (12) and to glycine. Arginine was selected because it is considered to be the prototypical amino acid secretagogue. Glycine was selected because it is the major amino acid in gelatin. As indicated earlier, gelatin strongly stimulates insulin secretion in persons with type 2 diabetes. This occurs even though glycine, when infused intravenously in a large amount, has been reported to have no effect on the glucose, insulin, or glucagon concentration in obese subjects who fasted overnight (13).

Many years ago it was reported that glycine given orally in amounts of 40–50 g results in a moderate reduction in blood glucose concentrations in healthy and diabetic adults [from 5.7 to 4 mmol/L (102 to 72 mg/dL) in healthy subjects and from 14.2 to 8.9 mmol/L (256 to 161 mg/dL) in diabetic subjects] (14, as quoted in 15). Others reported no effect on the blood glucose concentration in fasting subjects (16, 17, as quoted in 15). At that time, it was not possible to measure serum insulin concentrations.

Subsequently, glycine (0.3 mol) administered orally or intraduodenally was reported to have no effect on the blood glucose or insulin concentration over 180 min in overnight-fasted healthy subjects or in subjects with a partial gastrectomy. Serum glycine concentrations were increased {approx}3-fold. In subjects with mild untreated diabetes, the authors also stated that intraduodenally administered glycine did not affect either the glucose or the insulin concentration. Interestingly, glycine administration stimulated a rise in growth hormone in the nondiabetic but not in the diabetic subjects (11).

In the present study, ingestion of 1 mmol glycine/kg lean body mass ({approx}4.6 g) also did not significantly affect the plasma glucose concentration. It clearly stimulated an increase in insulin, although the increase was modest (Figures 2 and 3GoGo). The glycine was rapidly absorbed and the dose used increased the circulating glycine concentration by {approx}4-fold.

After this manuscript was submitted for publication, an article reporting the effect of glycine on insulin secretion and action in healthy first-degree relatives of patients with type 2 diabetes was published by Gonzalez-Ortiz et al (18). These authors reported an increase in peripheral insulin concentrations in 6 volunteers who received 5 g glycine orally 30 min before a hyperglycemic, hyperinsulinemic clamp. A small increase in insulin concentrations in 6 other volunteers who received a placebo (magnesium oxide) also was reported, but was only approximately one-quarter of that after glycine. Insulin action was not significantly different between the 2 groups. Thus, although both the experimental design and the patient population differed between our study and that of Gonzalez-Ortiz et al, the increase in peripheral insulin concentration after oral glycine administration was observed in both.

In the present study, glycine also resulted in a large increase in glucagon concentrations (Figure 4Go). Intravenously administered glycine potently stimulates glucagon secretion in dogs (19). However, even supraphysiologic concentrations of glycine, obtained by intravenous administration of the amino acid, do not increase the glucagon concentration in humans (13). Because intravenously administered glycine does not stimulate a rise in glucagon concentration, but oral glycine was rather potent in this regard, the current data suggest that the rise in glucagon was due to the release of a glucagon-stimulating hormone in response to glycine in the lumen of the gastrointestinal tract. However, to our knowledge, such a gut hormone has not been identified. In the same study, intravenously infused glycine also did not stimulate an increase in insulin concentration (13). However, when given orally in the present study, glycine did stimulate a modest increase in insulin. Thus, the same putative gut hormone may stimulate insulin secretion as well.

The dramatic reduction in the glucose area response when glycine was ingested with glucose is of considerable interest from a physiologic point of view. However, the mechanism remains to be determined. The integrated insulin area response after the ingestion of glycine + glucose was essentially the same as when only glucose was ingested, but it occurred at a greatly attenuated increase in glucose concentration and without a delay in the return of the glucose concentration to the initial fasting value. This result is similar to that we and others observed in healthy subjects when fat was ingested with glucose (20, 21). It suggests that the glucose clearance rate was accelerated. The clearance rate of ingested glucose was not determined in any of these studies. Therefore, whether the attenuated increase in glucose and rapid return to the fasting value was due to 1) an increased removal rate either directly or indirectly as a result of the rise in insulin, 2) an independent mechanism, or 3) a decrease in the endogenous glucose production rate cannot be determined.

A decrease in the glucose production rate would not be expected in the presence of a persistent large increase in the glucagon concentration. In fact, one would anticipate an increase in glucose production. A reduction in the glucose absorption rate also is unlikely but cannot be ruled out. Glycine has been reported to compete with glucose for absorption (22). Cholecystokinin and glucagon-like peptide 1 (GLP-1,7-36 amide) strongly reduce the rate of gastric emptying. The latter hormone also may reduce duodenal motility (23). Intraduodenal instillation of a mixture of nutritionally required amino acids stimulates cholecystokinin secretion; individually, phenylalanine, valine, and methionine were most potent. Nonnutritionally required amino acids including glycine did not stimulate cholecystokinin secretion (24). GLP-1 also stimulates insulin secretion and reduces glucagon secretion. Because glycine stimulated an increase in both insulin and glucagon, a glycine-stimulated increase in GLP-1 is not likely to explain the results (23). Overall, the data suggest that oral glycine stimulates the secretion, either directly or indirectly, of a gut hormone that potentiates or is additive with the effect of insulin in stimulating the removal of glucose from the circulation. It also inhibits the effect of glucagon on endogenous glucose production. Nevertheless, this remains only a speculation at present.

In any regard, the ingested glycine effect on the postprandial glucose concentration may be important therapeutically if a similar effect can be shown in persons with type 2 diabetes. It will also be of interest to determine whether glycine synergistically facilitates insulin secretion by other amino acids that are quantitatively prominent in gelatin protein.


   ACKNOWLEDGMENTS
 
We thank the subjects for participating in the study, the staff of the Special Diagnostic and Treatment Unit, the staff of the Clinical Chemistry Laboratory, the staff of the Nuclear Medicine Department, SK Nair and Dawn Morse for amino acid determinations, Mary J Adams for technical assistance, Terry Masai and the Ajinomoto Company for supplying the amino acid, and Michael A Kuskowski for advice on statistical analysis and presentation of the data.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Gannon MC, Nuttall FQ. Food protein and diabetes. In: Franz MJ, Bantle JP, eds. The health professional’s guide to medical nutrition therapy for diabetes. Alexandria, VA: American Diabetes Association, 1999:107–25.
  2. Gannon MC, Nuttall JA, Damberg G, Gupta V, Nuttall FQ. Effect of protein ingestion on the glucose appearance rate in subjects with type 2 diabetes. J Clin Endocrinol Metab 2001;86:1040–7.[Abstract/Free Full Text]
  3. Nuttall FQ, Mooradian AD, Gannon MC, Billington CJ, Krezowski PA. Effect of protein ingestion on the glucose and insulin response to a standardized oral glucose load. Diabetes Care 1984;7:465–70.[Abstract]
  4. Gannon MC, Nuttall FQ, Neil BJ, Westphal SA. The insulin and glucose responses to meals of glucose plus various proteins in type II diabetic subjects. Metabolism 1988;37:1081–8.[Medline]
  5. Hulten HO. Characteristics of muscle tissue. In: Fennema O, ed. Food chemistry. New York: Dekker, 1985:725–89.
  6. National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes 1979;28:1039–57.[Medline]
  7. Fuller G, Parker RM. Approximate integration. Applications 13–16. Analytical geometry and calculus. Princeton, NJ: Van Nostrand, 1964:367–8.
  8. McGilvery RW, Goldstein GW. Biochemistry. A functional approach. 3rd ed. Philadelphia: WB Saunders Company, 1983.
  9. Hamosh A, Johnston MV. Nonketotic hyperglycinemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic & molecular bases of inherited disease. 8th ed. New York: McGraw-Hill, 2001:206–7.
  10. Floyd JC Jr, Fajans SS, Pek S, Thiffault CA, Knopf RF, Conn JW. Synergistic effect of essential amino acids and glucose upon insulin secretion in man. Diabetes 1970;19:109–15.[Medline]
  11. Kasai K, Kobayashi M, Shimoda S-I. Stimulatory effect of glycine on human growth hormone secretion. Metabolism 1978;27:201–8.[Medline]
  12. Gannon MC, Nuttall JA, Nuttall FW. Oral arginine does not stimulate an increase in insulin concentration but delays glucose disposal. Am J Clin Nutr 2002;76:1016–22.[Abstract/Free Full Text]
  13. Muller WA, Aoki TT, Cahill GFJ. Effect of alanine and glycine on glucagon secretion in postabsorptive and fasting obese man. J Clin Endocrinol Metab 1975;40:418–25.[Abstract]
  14. Schenck EG. Über die Beeinflussbarkeit der Blutzuckerregulation durch Eiweisstoffe, Aminosäuren und deren Derivative. (Regulation of blood glucose by proteins, amino acids, and their derivatives.) Arch Exp Path Pharmakol 1932;167:201–15 (in German).
  15. Cochrane WA, Payne WW, Simpkiss MJ, Woolf LI. Familial hypoglycemia precipitated by amino acids. J Clin Invest 1956;35:411–22.
  16. Kanai I. Über den Einfluss von Aminosäuren auf den Blutzucker. (Effects of amino acids on blood glucose regulation.) Biochem Z 1932;248:383–8 (in German).
  17. Chikano M. Über den Einfluss von Aminosäuren und ihren Abkömmlingen auf die Adrenalinhyperglykämie. (Effect of amino acids and their derivatives on epinephrine hyperglycemia.) Biochem Z 1929;205:154–65 (in German).
  18. Gonzalez-Ortiz M, Medina-Santillan R, Martinez-Abundis E, von Drateln CR. Effect of glycine on insulin secretion and action in healthy first-degree relatives of type 2 diabetes mellitus patients. Horm Metab Res 2001;33:358–60.[Medline]
  19. Rocha DM, Faloona GR, Unger RH. Glucagon-stimulating activity of 20 amino acids in dogs. J Clin Invest 1972;51:2346–51.
  20. Gannon MC, Nuttall FQ, Westphal SA, Seaquist ER. The effect of fat with carbohydrate on plasma glucose, insulin, C-peptide and triglycerides in normal male subjects. J Am Coll Nutr 1993;12:36–41.[Abstract]
  21. Collier G, O’Dea K. The effect of coingestion of fat on the glucose, insulin, and gastric inhibitory polypeptide responses to carbohydrate and protein. Am J Clin Nutr 1983;37:941–4.[Abstract/Free Full Text]
  22. Cori CF. The absorption of glycine and D,L-alanine. Proc Exp Biol Med 1927;24:125–6.
  23. Nauck MA, Niedereichholz U, Ettler R, et al. Glucagon-like peptide 1 inhibition of gastric emptying outweighs its insulinotropic effects in healthy humans. Am J Physiol 1997;273:E981–8.[Abstract/Free Full Text]
  24. Go VLW, Hofmann AF, Summerskill WHJ. Pancreozymin bioassay in man based on pancreatic enzyme secretion. J Clin Invest 1970;49:1558–64.
Received for publication August 22, 2001. Accepted for publication January 24, 2002.




This article has been cited by other articles:


Home page
 J. Nutr.Home page
R. Hageman, C. Severijnen, B. J. M. van de Heijning, H. Bouritius, N. van Wijk, K. van Laere, and E. M. van der Beek
A Specific Blend of Intact Protein Rich in Aspartate Has Strong Postprandial Glucose Attenuating Properties in Rats
J. Nutr., September 1, 2008; 138(9): 1634 - 1640.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
D. K Layman, P. Clifton, M. C Gannon, R. M Krauss, and F. Q Nuttall
Protein in optimal health: heart disease and type 2 diabetes
Am. J. Clinical Nutrition, May 1, 2008; 87(5): 1571S - 1575S.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
A. Karamanlis, R. Chaikomin, S. Doran, M. Bellon, F D. Bartholomeusz, J. M Wishart, K. L Jones, M. Horowitz, and C. K Rayner
Effects of protein on glycemic and incretin responses and gastric emptying after oral glucose in healthy subjects
Am. J. Clinical Nutrition, November 1, 2007; 86(5): 1364 - 1368.
[Abstract] [Full Text] [PDF]

Home page
 J. Nutr.Home page
C. Blouet, F. Mariotti, D. Azzout-Marniche, C. Bos, V. Mathe, D. Tome, and J.-F. Huneau
The Reduced Energy Intake of Rats Fed a High-Protein Low-Carbohydrate Diet Explains the Lower Fat Deposition, but Macronutrient Substitution Accounts for the Improved Glycemic Control
J. Nutr., July 1, 2006; 136(7): 1849 - 1854.
[Abstract] [Full Text] [PDF]

Home page
 J. Physiol.Home page
A. Gameiro, F. Reimann, A. M. Habib, D. O'Malley, L. Williams, A. K. Simpson, and F. M. Gribble
The neurotransmitters glycine and GABA stimulate glucagon-like peptide-1 release from the GLUTag cell line
J. Physiol., December 15, 2005; 569(3): 761 - 772.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
P. S Parimi, S. Devapatla, L. L Gruca, S. B Amini, R. W Hanson, and S. C Kalhan
Effect of enteral glutamine or glycine on whole-body nitrogen kinetics in very-low-birth-weight infants
Am. J. Clinical Nutrition, March 1, 2004; 79(3): 402 - 409.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q
Agricola
Right arrow Articles by Gannon, M. C
Right arrow Articles by Nuttall, F. Q

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS