Influence of age on contractile response to insulin-like growth factor 1 in ventricular myocytes from spontaneously hypertensive rats.
- 1 December 1999
- journal article
- other
- Published by Wolters Kluwer Health in Hypertension
- Vol. 34 (6) , 1215-1222
- https://doi.org/10.1161/01.hyp.34.6.1215
Abstract
Abstract —Evidence suggests a pathophysiological role of insulin-like growth factor 1 (IGF-1) in hypertension. Cardiac function is altered with advanced age, similar to hypertension. Accordingly, the effects of IGF-1 on cardiac myocyte shortening and intracellular Ca 2+ were evaluated in hypertension at different ages. Ventricular myocytes were isolated from Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR), aged 12 and 36 weeks. Mechanical and intracellular Ca 2+ properties were examined by edge-detection and fluorescence microscopy. At 12 weeks, IGF-1 (1 to 500 ng/mL) increased peak twitch amplitude (PTA) and FFI changes (ΔFFI) in a dose-dependent manner in WKY myocytes, with maximal increases of 27.5% and 35.2%, respectively. However, IGF-1 failed to exert any action on PTA and ΔFFI in the age-matched SHR myocytes. Interestingly, at 36 weeks, IGF-1 failed to exert any response in WKY myocytes but depressed both PTA and ΔFFI in a dose-dependent manner in SHR myocytes, with maximal inhibitions of 40.5% and 16.1%, respectively. Myocytes from SHR or 36-week WKY were less sensitive to norepinephrine (1 μmol/L) and KCl (30 mmol/L). Pretreatment with nitric oxide synthase inhibitor N ω -nitro- l -arginine methyl ester (L-NAME, 100 μmol/L) did not alter the IGF-1–induced response in 12-week WKY myocytes but unmasked a positive action in 12-week SHR and 36-week WKY myocytes. L-NAME also significantly attenuated IGF-1–induced depression in 36-week SHR myocytes. In addition, the Ca 2+ channel opener Bay K8644 (1 μmol/L) abolished IGF-1–induced cardiac depression in 36-week SHR myocytes. Collectively, these results suggest that the IGF-1–induced cardiac contractile response was reduced with advanced age as well as with hypertension. Alterations in nitric oxide and intracellular Ca 2+ modulation may underlie, in part, the resistance to IGF-1 in hypertension and advanced age.Keywords
This publication has 20 references indexed in Scilit:
- Influence of Age on Inotropic Response to Insulin and Insulin-Like Growth Factor I in Spontaneously Hypertensive Rats: Role of Nitric OxideExperimental Biology and Medicine, 1999
- Increased expression of low-affinity insulin receptor isoform and insulin/insulin-like growth factor-I hybrid receptors in term placenta from insulin-resistant women with gestational hypertensionDiabetologia, 1996
- The effect of insulin-like growth factor-1 on adult rat cardiac contractilityMolecular and Cellular Biochemistry, 1996
- Insulin-like growth factor I and its binding proteins in the cardiovascular systemCardiovascular Research, 1995
- Ionic basis of action potential prolongation of hypertrophied cardiac myocytes isolated from hypertensive rats of different agesCardiovascular Research, 1994
- Direct demonstration of insulin-like growth factor-I-induced nitric oxide production by endothelial cellsKidney International, 1994
- Insulin-like growth factor 1 and sodium???lithium countertransport in essential hypertension and in hypertensive left ventricular hypertrophyJournal Of Hypertension, 1993
- Impairment of Myocyte Contractility Following Coronary Artery Narrowing Is Associated with Activation of the Myocyte IGF1 Autocrine System, Enhanced Expression of Late Growth Related Genes, DNA Synthesis, and Myocyte Nuclear Mitotic Division in RatsExperimental Cell Research, 1993
- Enhanced Glucose Tolerance in Spontaneously Hypertensive Rats: Pancreatic β-Cell Hyperfunction With Normal Insulin SensitivityDiabetes, 1992
- Insulin-like growth factors and insulin increase the contractility of neonatal rat cardiocytes in vitroBasic Research in Cardiology, 1988