Maladaptive Remodeling of Cardiac Myocyte Shape Begins Long Before Failure in Hypertension

Hypertension - Tập 32 Số 4 - Trang 753-757 - 1998
Tatsuyuki Onodera1,2, Tetsutaro Tamura1,2, Suleman Said1,2, Sylvia A. McCune1,2, A. Martin Gerdes1,2
1From the Department of Anatomy and Structural Biology, University of South Dakota, Vermillion (T.O., T.T., S.S., A.M.G.), and the South Dakota Cardiovascular Research Institute, Sioux Falls (T.T., S.S., A.M.G.), SD; and the Department of Food Science and Technology, Ohio State University, Columbus, Ohio (S.A.M.).
2the Department of Food Science and Technology, Ohio State University, Columbus, Ohio (S.A.M.).

Tóm tắt

Abstract —Progression to failure in hypertension is associated with ventricular dilation, excessive myocyte lengthening, and an increase in myocyte length/width ratio. The temporal development of these changes in relation to impaired pump performance is unknown. We examined isolated myocytes from 1- to 12-month-old spontaneously hypertensive heart failure (SHHF) rats who develop heart failure at approximately 24 months of age. Left ventricular myocyte cross-sectional area reached a maximum of ≈350 to 400 μm 2 at 3 months of age and did not change significantly thereafter. Nonetheless, LV systolic wall stress, a known stimulus for myocyte transverse growth, increased progressively between 3 and 12 months of age. Unlike the situation in normally aging rats with stable body mass, myocyte length in SHHF rats continued to increase with aging ( P <0.05 from 9 to 12 months of age). In summary, (1) left ventricular myocyte transverse growth reaches an upper limit by 3 months of age although systolic wall stress continues to rise; and (2) cell length is significantly increased by 12 months of age. This study suggests that maladaptive remodeling of cardiac myocyte shape begins long before pump failure in hypertension. Additionally, it appears that the left ventricle may be robbed of an important adaptive mechanism to normalize wall stress (eg, myocyte transverse growth) early in the progression to failure.

Từ khóa


Tài liệu tham khảo

Werchan PM, Summer WR, Gerdes AM, McDonough KH. Right ventricular performance following monocrotaline-induced pulmonary hypertension. Am J Physiol. 1989;256:H1328–H1336.

10.1097/00005344-199009000-00019

10.1161/res.69.3.1714799

10.1161/hyp.28.4.609

Gerdes AM. Chronic ischemic heart disease. In: Weber KT ed. Wound Healing in Cardiovascular Disease. Armonk NY: Futura Publishing Co; 1995:61–66.

10.1161/circ.86.2.1638711

10.1016/0022-2828(95)90000-4

10.1093/ilar.32.3.23

McCune SA Radin MJ Jenkins JE Chu YY Park S. SHHF/Mcc-fa cp rat model: effects of gender and genotype on age of expression of metabolic complications and congestive heart failure and on response to drug therapy. In: Shafir E ed. Lessons From Animal Diabetes V. Smith-Gordon UK: 1995:255–270.

McCune SA Park S Radin MJ Jurin RR. The SHHF/Mcc-facp rat model: a genetic model of congestive heart failure. In: Singal PK Dixon IMC Beamish RE Dhalla NS eds. Mechanisms of Heart Failure. Boston Mass: Kluwer Academic Publishers; 1995:91–106.

10.1002/ar.1092260210

10.1161/circ.91.10.2642

10.1002/ar.1092150414

10.1161/res.42.2.620442

10.1161/res.47.1.7379260

10.1002/ar.1092190110

10.1172/JCI108079

Terracio L, Borg TK. Factors affecting cardiac cell shape. Heart Failure. 1988;4:114–124.

10.1006/jmcc.1996.0204

10.1016/S0021-9258(18)68649-1

10.1161/res.73.3.8348687

10.1074/jbc.271.16.9535

10.1016/0002-9149(73)91030-8

10.1161/circ.86.1.1535573

10.1161/circ.83.6.1828192

10.1161/res.81.2.137