The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Metabolism of C-peptide in the dog. In vivo demonstration of the absence of hepatic extraction.
Open accessAbstract
The in vivo hepatic metabolism of connecting peptide (C-peptide) in relation to that of insulin has not been adequately characterized. A radioimmunoassay for dog C-peptide was therefore developed and its metabolism studied in conscious mongrel dogs, with sampling catheters chronically implanted in their portal and hepatic veins and femoral artery. The hepatic extraction of endogenous C-peptide under basal conditions was negligible (4.3 +/- 4.5%) and was similar to the hepatic extraction of C-peptide measured during the constant exogenous infusion of C-peptide isolated from dog pancreas. Simultaneously measured hepatic extraction of endogenous and exogenously infused insulin were 43.8 +/- 7.6 and 47.5 +/- 4.4%, respectively. The metabolic clearance rate of infused C-peptide was 11.5 +/- 0.8 ml/kg per min and was constant over the concentration range usually encountered under physiological conditions. In additional experiments, the effect of parenteral glucose administration on the hepatic extraction of C-peptide and insulin was investigated. The hepatic extraction of C-peptide (6.2 +/- 4.0%) was again negligible in comparison with that of insulin (46.7 +/- 3.4%). Parenteral glucose administration did not affect the hepatic extraction of either peptide irrespective of whether it was infused peripherally, intraportally, or together with an intraportal infusion of gastrointestinal inhibitory polypeptide. The fasting C-peptide insulin molar ratio in both the portal vein (1.2 +/- 0.1) and femoral artery (2.1 +/- 0.3) was also unaffected by the glucose stimulus. These results therefore indicate that, since the hepatic extraction of C-peptide is negligible and its clearance kinetics linear, the peripheral C-peptide concentration should accurately reflect the rate of insulin secretion. New approaches to the quantitation of hepatic extraction and secretion of insulin by noninvasive techniques are now feasible.
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“Glucocorticoids have been previously shown to induce peripheral hyperinsulinemia because of prehepatic β-cell insulin hypersecretion that is partially ameliorated by a concomitant increase of hepatic insulin clearance,22,23 but not with C-peptide as GCs do not affect hepatic extraction of C-peptide24, and the clearance kinetics of C-peptide is linear.25”
From Twenty‐four‐hour profiles of plasma glucose, insulin, C‐peptide and free fatty acid in subjects with varying degrees of glucose tolerance following short‐term, medium‐dose prednisone (20 mg/day) treatment: evidence for differing effects on insulin secretion and action (2012) · cites this paper as [25]
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Morgan, C. R., & Lazarow, A. (1963) · Diabetes · doi:10.2337/diab.12.2.115 · Cited by 2,197
Determination of Free and Total Insulin and C-Peptide in Insulin-treated Diabetics
Kuzuya, H., BLIX, P. M., Horwitz, D. L., Steiner, D. F., & Rubenstein, A. H. (1977) · Diabetes · doi:10.2337/diab.26.1.22 · Cited by 603
Self-citationProinsulin, insulin, and C-peptide concentrations in human portal and peripheral blood.
Horwitz, D. L., Starr, J. I., Mako, M. E., Blackard, W. G., & Rubenstein, A. H. (1975) · Journal of Clinical Investigation · doi:10.1172/jci108047 · Cited by 473
Self-citationC-peptide Response to Glucagon: A Test for the Residual β-cell Function in Diabetes Mellitus
FABER, O. K., & Binder, C. (1977) · Diabetes · doi:10.2337/diab.26.7.605 · Cited by 396
Prehepatic Insulin Production in Man: Kinetic Analysis Using Peripheral Connecting Peptide Behavior*
EATON, R. P., ALLEN, R. C., SCHADE, D. S., ERICKSON, K. M., & STANDEFER, J. (1980) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-51-3-520 · Cited by 363
Peterson, J. D., Nehrlich, S. C., Oyer, P. E., & Steiner, D. F. (1972) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)44991-0 · Cited by 301
Secretion of Proinsulin C-Peptide by Pancreatic β Cells and its Circulation in Blood
Rubenstein, A. H., Clark, J. L., Melani, F., & Steiner, D. F. (1969) · Nature · doi:10.1038/224697a0 · Cited by 295
Self-citationMetabolism of Proinsulin, Insulin, and C-Peptide in the Rat
Katz, A. I., & Rubenstein, A. H. (1973) · Journal of Clinical Investigation · doi:10.1172/jci107277 · Cited by 265
Self-citationDetermination of free and total insulin and C-peptide in insulin-treated diabetics
Kuzuya, H., BLIX, P. M., Horwitz, D. L., et al. (1977) · Diabetes · doi:10.2337/diabetes.26.1.22 · Cited by 170
The Metabolism of Proinsulin and Insulin by the Liver
Rubenstein, A. H., Pottenger, L. A., Mako, M. E., Getz, G. S., & Steiner, D. F. (1972) · Journal of Clinical Investigation · doi:10.1172/jci106886 · Cited by 159
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Research works printed but not linked: 1
- Bock, R. D. 1975. Statistical Methods in Behavioural Research. McGraw-Hill, Inc., New York. 447.
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Sorted by citations
Reduced incretin effect in Type 2 (non-insulin dependent) diabetes
Nauck, M., Stöckmann, F., Ebert, R., & Creutzfeldt, W. (1986) · Diabetologia · doi:10.1007/bf02427280 · Cited by 1,307
Palmer, J. P., Fleming, G. A., Greenbaum, C. J., Herold, K. C., Jansa, L. D., Kolb, H., Lachin, J. M., Polonsky, K. S., Pozzilli, P., Skyler, J. S., et al. (2004) · Diabetes · doi:10.2337/diabetes.53.1.250 · Cited by 491
Self-citationPolonsky, K. S., Licinio-Paixao, J., Given, B. D., Pugh, W., Rue, P., Galloway, J., Karrison, T., & Frank, B. (1986) · Journal of Clinical Investigation · doi:10.1172/jci112308 · Cited by 359
Self-citationSplanchnic insulin metabolism in obesity. Influence of body fat distribution.
Peiris, A. N., Mueller, R. A., Smith, G. A., Struve, M. F., & Kissebah, A. H. (1986) · Journal of Clinical Investigation · doi:10.1172/jci112758 · Cited by 346
The renal metabolism of insulin
Rabkin, R., Ryan, M. P., & Duckworth, W. C. (1984) · Diabetologia · doi:10.1007/bf00304849 · Cited by 294
Metadata
- Authors
- Polonsky, K., Jaspan, J., Pugh, W., Cohen, D., Schneider, M., Schwartz, T., Moossa, A. R., Tager, H., & Rubenstein, A. H.
- Affiliations
- University of Chicago (US)
- ORCID
- Schwartz, T
- Venue
- Journal of Clinical Investigation
- Published
- 1983-09-01
- Volume
- 72
- Issue
- 3
- Pages
- 1114-1123
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC1129279
- OpenAlex
- W1963481139
- Cited by
- 158
- References
- 29
- Citations by year
- 2024: 2 · 2022: 2 · 2021: 3 · 2020: 2 · 2019: 3 · 2018: 6 · 2017: 1 · 2016: 3 · 2014: 1 · 2013: 5 · 2012: 1
- FWCI
- 14.66
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Diabetes Association
- National Institutes of Health (5r01am031842-03, 5r01am018347-12, 5r01am025913-07)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Keywords
- C-peptide, hepatic extraction, hepatic metabolism, insulin, metabolic clearance rate, glucose stimulation, portal vein, insulin secretion, radioimmunoassay, dogs
- MeSH terms
- Animals, Blood Glucose, C-Peptide, Dogs, Femoral Artery, Glucose, Hepatic Veins, Insulin, Liver, Metabolic Clearance Rate, Peptides, Radioimmunoassay
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