Closing in on the Mechanisms of Pulsatile Insulin Secretion
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Bertram, Richard
[1
,2
,3
]
Satin, Leslie S.
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Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Brehm Ctr Diabet Res, Ann Arbor, MI USAFlorida State Univ, Dept Math, Tallahassee, FL 32306 USA
Satin, Leslie S.
[4
,5
]
Sherman, Arthur S.
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NIDDK, Lab Biol Modeling, NIH, Bethesda, MD 20892 USAFlorida State Univ, Dept Math, Tallahassee, FL 32306 USA
Sherman, Arthur S.
[6
]
机构:
[1] Florida State Univ, Dept Math, Tallahassee, FL 32306 USA
[2] Florida State Univ, Program Neurosci, Tallahassee, FL 32306 USA
[3] Florida State Univ, Program Mol Biophys, Tallahassee, FL 32306 USA
[4] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Brehm Ctr Diabet Res, Ann Arbor, MI USA
[6] NIDDK, Lab Biol Modeling, NIH, Bethesda, MD 20892 USA
Insulin secretion from pancreatic islet beta-cells occurs in a pulsatile fashion, with a typical period of similar to 5 min. The basis of this pulsatility in mouse islets has been investigated for more than four decades, and the various theories have been described as either qualitative or mathematical models. In many cases the models differ in their mechanisms for rhythmogenesis, as well as other less important details. In this Perspective, we describe two main classes of models: those in which oscillations in the intracellular Ca2+ concentration drive oscillations in metabolism, and those in which intrinsic metabolic oscillations drive oscillations in Ca2+ concentration and electrical activity. We then discuss nine canonical experimental findings that provide key insights into the mechanism of islet oscillations and list the models that can account for each finding. Finally, we describe a new model that integrates features from multiple earlier models and is thus called the Integrated Oscillator Model. In this model, intracellular Ca2+ acts on the glycolytic pathway in the generation of oscillations, and it is thus a hybrid of the two main classes of models. It alone among models proposed to date can explain all nine key experimental findings, and it serves as a good starting point for future studies of pulsatile insulin secretion from human islets.
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Univ Virginia, Dept Med, Div Endocrinol & Metab, Charlottesville, VA 22901 USAUniv Virginia, Dept Med, Div Endocrinol & Metab, Charlottesville, VA 22901 USA
Nunemaker, Craig S.
Satin, Leslie S.
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Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48105 USA
Univ Michigan, Sch Med, Brehm Diabet Res Ctr, Ann Arbor, MI 48105 USAUniv Virginia, Dept Med, Div Endocrinol & Metab, Charlottesville, VA 22901 USA
机构:
Univ Michigan, Dept Pharmacol, Med Sch, Ann Arbor, MI 48109 USA
Univ Michigan, Brehm Ctr Diabet Res, Med Sch, Ann Arbor, MI 48109 USANIH, Lab Biol Modeling, Bldg 10, Bethesda, MD 20892 USA
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UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT MED,DIV ENDOCRINOL,TORRANCE,CA 90509UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT MED,DIV ENDOCRINOL,TORRANCE,CA 90509
CHOU, HF
IPP, E
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UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT MED,DIV ENDOCRINOL,TORRANCE,CA 90509UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT MED,DIV ENDOCRINOL,TORRANCE,CA 90509