Abstract
Recent data indicates that impaired insulin action predisposes to increased vascular smooth muscle [1-26] (VSM) tone, the hallmark of hypertension associated with diabetes mellitus. This research has established VSM as an “insulin sensitive tissue” like skeletal muscle tissue and adipocytes. Insulin and insulin-like growth factor (IGF-I) regulate VSM intracellular cation metabolism through attenuating effects on inward calcium (Ca2+) currents [1 10 15 27 28] and by direct effects on VSMNa+,K+-ATPase pump expression and activity[29 30] and that IGF-I and insulin stimulate glucose uptake in VSM cells (VSMC). IGF-1 and insulin are structurally related [17] share receptors [17 18] and have similar post-receptor actions [17 18] (Figure 1). Unlike insulin, which must transverse the endothelium before acting on VSMC in vivo, IGF-1 is synthesized by VSMC [19]. Thus, IGF-1 may have more relevance than insulin in VSMC physiology.
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References
Epstein M And Sowers J. Diabetes mellitus and hypertension. Hypertension 1992;19:403–418.
Sowers JR, Sowers PS, Peuler JD. Role of insulin resistance and hyperinsulinemia in development of hypertension and atherosclerosis. Journ Lab Clin Med 1994;123:647–652.
Anderson EA, Hoffman RP, Balon TW, et al. Hyperinsulinemia produces both sympathetic neural activation and vasodilation in normal humans. J Clin Invest 1991;87:2246–2252.
Sowers JR. At the cutting edge: Insulin resistance and hypertension. Mol Cell Endocrinol 1990;4: C87–C89.
Baron AD, Brechtel-Hoals G, Johnson A, et al. Skeletal muscle blood flow: A possible link between insulin resistance and blood pressure. Hypertension 1993;21:129–135.
Yagi S, Takata S, Kiyokawa H, et al. Effects of insulin on vasoconstrictive responses to norepinephrine and angiotensin II in rabbit femoral artery and vein. Diabetes 1992;37:1064–1067.
Hall JE, Coleman TG, Mizelle FIL, et al. Chronic hyperinsulinemia and blood pressure regulation. Am J Physiol 1990;27:F722–F731.
Sowers JR, Khoury S, Standley PR, et al. Mechanisms of hypertension in diabetes. Am J Hypertens 1991;4:177–182.
Sowers JR, Standley PR, Ram JL, et al. Hyperinsulinemia, insulin resistance and hyperglycemia. Contributing factors in the pathogenesis of hypertension and atherosclerosis. Am J Hypertens 1993;6:260–270.
Ram JL, Fares MA, Standley PR, Sowers JR. Insulin inhibits vasopressin contraction of vascular smooth muscle cells. J Vasc Biol 1993;4:250–254.
Kahn AM, Seidel CL, Allen JC, O’Neil RG, Shelat H, Song T. Insulin reduces contraction and intracellular calcium concentration in vascular smooth muscle. Hypertension 1993;22:735–742.
Wang G, Glover KW, Dunlap RC, et al. Antagonism of endothelium derived relaxing factor (EDRF) production prevents hypotensive response to insulin. FASEB J 1993;7:A616.
Hirschberg R, Kopple JD. Evidence that insulin-like growth factor I increases renal plasma flow and glomerular filtration rate in fasted rats. J Clin Invest 1989; 83(1):326–330.
Yu H-Y, Jeng YY, Yue C-J, et al. Endothelial-dependent vascular effects of insulin and insulin-like growth factor I in the perfused rat mesenteric artery and aortic ring. Diabetes 1994;43:1027–1032.
Hu Y, Pete GM, Walsh MF, Sowers JR, Dunbar JC. IGF-I alters blood pressure and blood flow in normal rats: The effect of systemic vs. intracerebroventricular (ICV) administration. FAC Experimental Biology (abstract) 1995.
Kerr D, Tamborlane WV, Rife F, Sherwin RS. Effects of Insulin-like Growth Factor-1 on the responses to and recognition of hypoglycemia in humans. J Clin Invest 1993;91:141–147.
Murphy LJ, Ghahary A, Chakrabarti S. Insulin regulation of IGF-I expression in rat aorta. Diabetes 1990;39:657–661.
Tartare S, Ballotti R, Van Oberrghen E. Interactions between heterologous receptor tyrosine kinases: hormone stimulated insulin receptors activate unoccupied IGF-1 receptors. FEBS Lett 1991;295;219–225.
Delafontaine P, Bernstein KE, Alexander RW. Insulin-like growth factor I gene expression in vascular cells. Hypertension 1991;17:693–699.
Fagin JA, Roberts CT, LeReith D. Coordinate decrease of tissue insulin-like growth factor I post-transcriptional alternative mRNA transcripts in diabetes mellitus. Diabetes 1989;38:428–434.
Frattuli AL, Treadway JL, Pessin JE. Insulin/IGF-1 hybrid receptors: Implications for dominant-negative phenotype in syndromes of insulin resistance. J Cell Biochem 1992;48(1):43–50.
Zemel MB, Peuler JD, Sowers JR, et al. Hypertension in insulin-resistant Zucker obese rats is independent of sympathetic neural support. Am J Phys 1992;262:E368–371.
Standley PR, Ram JL, Sowers JR. Insulin attenuation of vascular smooth muscle calcium responses in Zucker lean and obese rats. Endocrinology 1993;133;4:1693–1699.
Shehin SE, Sowers JR, et al. Impaired vascular smooth muscle 45Ca efflux and hypertension in Zucker obese rats. J Vasc Med Biol 1989;1:278–282.
Standley PR, Bakir MH, Sowers JR. Vascular insulin abnormalities, hypertension and accelerated atherosclerosis. Am J Kidney Dis 1993;6:39–46.
Reddy S, Shehin S, Sowers JR, et al. Aortic calcium-45 efflux and blood pressure regulation in streptozotocin-induced diabetic rats. J Vasc Med Biol 1990;2:46–51.
Standley PR, Zhang F, Ram JL, Sowers JR. Insulin attenuates vasopressin-induced calcium transients and a voltage-dependent calcium response in rat vascular smooth muscle cells. J Clin Invest 1991;88:1230–1236.
Hori MT, Fittinghof M, Tuck ML. Mechanism of insulin attenuation of calcium in cultured vascular smooth muscle cells. J Clin Invest 1993;92:1161–1167.
Tirupattur PR, Ram JL, Standley PR, Sowers JR. Regulation on Na’,K+-ATPase gene expression by insulin in vascular smooth muscle cells. Am J Hypertens 1993;6:626–629.
Simmons DA, Winegard AI. Insulin does not regulate vascular smooth muscle Na’,K+-ATPase activity in rabbit aorta. Diabetologia 1993;36:212–217.
Kotchen TA, Zhang HV, Covelli M, Blehsehmidt N. Insulin resistance and blood pressure in Dahl rats and in one-kidney, one-clip hypertensive rats. Am J Physiol 1991;261:E692–E697.
Reaven BM, Twersky J, Chang H. Abnormalities of carbohydrate and lipid metabolism in Dahl rats. Hypertension 1991;18:630–635.
Herrara VLM, Chobanian AV, Ruiz-Opazo N. Isoform-specific modulation of NA+,K+-ATPase a subunit gene expression in hypertension. Science 1988;241:221–223.
Sada T, Koike H, Ideda M, et al. Cytosolic free calcium of aorta in hypertensive rats. Hypertension 1990;16:245–251.
Standley RP, Rose K, Tirupathur PR, Sowers JR. Insulin stimulated glucose transport of vascular smooth muscles cells: Possible implications of GLUT-4 in the vasculature. Physiologist 1992;35:A13.
Standley PR, Rose KA, Sowers JR. Increased basal arterial smooth muscle glucose transport in the Zucker rat. Am J Hypertens, in press.
Brosius FC, Briggs JP, Marcus RG, et al. Insulin-responsive glucose transporter expression in renal microvessels and glomeruli. Kidney International 1992;42:1086–1092.
Bova S, Goldman WF, Yuan X-J, et al. Influence of Na+ gradient on Ca’ transients and contraction in vascular smooth muscle. Am J Physiol 1990;259(Heart Circ Physiol):H409–H423.
Reuter H. Sodium-calcium exchange: Ins and outs of CaZ+ transport. Nature 1991;349:567–568.
Lynch RM, Paul RJ. Compartmentalization of glycolytic and glycogenolytic metabolism in vascular smooth muscle. Science 1987;222:1344–1346.
Barron JT, Kapp SJ, Tow JP, Messer JV. Effect of altering carbohydrate metabolism on energy status and contractile function of vascular smooth muscle. Biochim Biophys Acta 1989;976:42–52.
Barron JT, Bárány K, Kopp SJ. Effects of ATP reduction of the pattern of force development and myosin light chain phosphorylation in intact arterial smooth muscle. Biochim Biophys Acta 1989;1010:278–282.
Hardin CD, Wiseman RW, Kushmerich MJ. Vascular oxidative metabolism under different metabolic conditions. Biochimica et Bioophysica Acta 1992;1133:133–141.
Lynch RM, Paul RJ. Glucose uptake in porcine carotid artery: Relation to alterations in active Na+-K+ transport. Am J Physiol 1984;247:C433–441.
Sussman I, Schultz V, Gupta S, et al. Differential effect of metabolic fuels on the energy state of the Na+,K+-ATPase in isolated cerebral microvessels. Am J Physiol 1993;265:E777–E782.
Schull GE, Greeb J, Lingrel JB. Molecular cloning of three distinct forms of the Na+,K--ATPase alpha-subunit from rat brain. Biochemistry 1986;25:8125–8132.
Sweadner KJ. Isozymes of the Na+/K+-ATPase. Biochim Biophys Acta 1989;988:185–220.
Resh MD, Nemenoff RA, Guidotti G. Insulin stimulation of Na+,K+-ATPase triphosphatase-dependent 86RB-uptake in rat adipocytes. J Biol Chem 1990;255:10938–10945.
Clausen T, Everts ME. Regulation of the Na,K-pump in skeletal muscle. Kidney Int 1989;35:1–13.
O’Hare T, Sussman KE, Draznin B. Effect of diabetes on cytosolic free Ca“ and Nat-K+-ATPase in rat aorta. Diabetes 1991;40:1560–1563.
Omatsu-Kanbe M, Kitasato H. Insulin stimulates the translocation of Na+/K+dependent ATPase molecules from intracellular stores to the plasma membrane in frog skeletal muscle. Biochem J 1990;272:727–733.
Nishida K, Ohara T, Johnson J, et al. Na+/K+-ATPase activity and its alpha II subunit gene expression in rat skeletal muscle: Influence of diabetes, fasting, and refeeding. Metab Clin Exp 1992;41:56–63.
Hundal HS, Maritto A, Mitsumato Y, et al. Insulin induces translocation of the a2 and 131 subunits of the Na’/K+-ATPase from intracellular compartments to the plasma membranes in mammalian skeletal muscle. J Biol Chem 1992;267(8):5040–5043.
Sampson SR, Bak A, Krok S, et al. Effects of insulin-like growth factors on the expression of Na-channels and Na,K pump in cultured skeletal muscle (Abstract), Prod Int AGF Symp 2nd San Francisco 1991;B35.
Everts ME, Dorup I, Flyvbjerg A, et al. NatK+ pump in rat muscle: Effects of hypophysectomy, growth hormone, and thyroid hormone. Am J Physiol 1990;259 (Endocrinol Metab 22):E278–E293.
Dorup I, Flyvbjerg A. Effects of IGF-1 infusion on growth and muscle Na+-K+- pump concentration in K’-deficient rats. Am J Physiol 1993;264:E810–815.
Thorens B, Charon MJ, Lodish HF. Molecular physiology of glucose transporters. Diabetes Care 1990;13:209–218.
Kahn BB. Facilitative glucose transporters. Regulatory mechanisms and dysregulation in diabetes. J Clin Invest 1992;89:1367–74.
Reusch JE-B, Begum N, Sussman KE, Draznin B. Regulation of GLUT-4 phosphorylation by intracellular calcium in adipocytes. Endocrinology 1991;129:3269.
Klip A. Acute and chronic signals controlling glucose transport in skeletal muscle. J Cell Biochem 1991;48:51–60.
Koranyi L, James D, Muechler M, Permutt MA. Glucose transporter levels in spontaneously obese (OB/OB) insulin-resistant mice. J Clin Invest 1990;85:962–967.
Hainault M, Suerre-Millo M, Suchard K, Larau M. Differential regulation of adipose tissue glucose transporters in genetic obesity (fatty rat). J Clin Invest 1991;87:1127–1131.
Horton ED, King PA, Hirshman MF, Horton ES. Failure of insulin to stimulate glucose transporter translocation in skeletal muscle from obese (Fa/fa) Zucker rat. Diabetes 1990;39:83A(abstr).
Lorenz JN, Schnermann J, Brosius FC, et al. Intracellular ATP can regulate afferent arteriolar tone via ATP-sensitive KC channels in the rabbit. J Clin Invest 1992;90:733–40.
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Sowers, J.R. (1995). Actions of Insulin and Igf-I on Vascular Smooth Muscle Cation and Glucose Metabolism. In: Godfraind, T., Mancia, G., Abbracchio, M.P., Aguilar-Bryan, L., Govoni, S. (eds) Pharmacological Control of Calcium and Potassium Homeostasis. Medical Science Symposia Series, vol 9. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0117-2_14
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