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在血管紧张素转换酶抑制基础上加用1型血管紧张素II受体阻滞剂可限制心肌梗死后心肌细胞重塑。

Adding angiotensin II type 1 receptor blockade to angiotensin-converting enzyme inhibition limits myocyte remodeling after myocardial infarction.

作者信息

Kim Young-Kwon, Mankad Sunil, Kim Song-Jung, Takagi Gen, Tamura Tetsutaro, Gerdes A Martin, Bishop Sanford P, Kramer Christopher M

机构信息

Department of Cell Biology and Molecular Medicine, UMDNJ-New Jersey Medical School, New Jersey, USA.

出版信息

J Card Fail. 2003 Jun;9(3):238-45. doi: 10.1054/jcaf.2003.32.

Abstract

BACKGROUND

Adding angiotensin II type 1 receptor blockade (ARB) to angiotensin-converting enzyme inhibition (ACEI) further attenuates left ventricular (LV) remodeling in an ovine model of myocardial infarction (MI). We hypothesized that combined therapy with ACEI and ARB (CT) would be additive in the limitation of the myocyte hypertrophy and dysfunction that occurs in untreated adjacent noninfarcted regions during remodeling.

METHODS AND RESULTS

Nineteen sheep underwent coronary ligation to create a moderate-sized anteroapical infarction. Post-MI day 2, sheep were randomized to therapy with ramipril (ACEI, n = 5) or ramipril plus losartan (CT, n = 6) or none (untreated, n = 8). Infarct size was similar between groups. At 8 weeks post-MI, myocytes were isolated from regions adjacent to and remote from the infarct to measure morphometric indices (cell volume, length, cross-sectional area, width) and parameters of contraction (% shortening and -dL/dt, rate of shortening) and relaxation (+dL/dt [rate of relengthening] and TR 70% [time for 70% relengthening]). Volume % collagen was measured from adjacent and remote regions. Adjacent myocyte volume was different between groups (2.5 +/- 0.1 x 10(4) microm(3) in CT, 3.0 +/- 0.4 x 10(4) microm(3) in ACEI, 3.5 +/- 0.2 x 10(4) microm(3) in untreated, analysis of variance [ANOVA] P =.001) as was length (158 +/- 4 microm, 161 +/- 9 microm, 189 +/- 8 microm, respectively, ANOVA P <.001). Adjacent cell volume and length in CT were lower than untreated (P <.05). Percent shortening and -dL/dt of isolated adjacent myocytes were improved with both ACEI (7.9 +/- 0.3%, -131 +/- 6 microm/sec, P <.05) and CT (7.7 +/- 0.3%, -144 +/- 8 microm/sec, P <.05) compared with no therapy (6.4 +/- 0.4%, -104 +/- 7 microm/sec), as was both +dL/dt and TR 70%. No between-group difference in volume % collagen was found in adjacent or remote regions.

CONCLUSION

Compared with ACEI alone, the addition of ARB further limits adjacent noninfarcted myocyte hypertrophy during post-MI LV remodeling. Both ACEI alone and CT preserve isolated unloaded myocyte function, but neither significantly reduce interstitial collagen. The additional benefit of ARB on regional and global function in vivo may also be due to other factors including regional load.

摘要

背景

在心肌梗死(MI)绵羊模型中,在血管紧张素转换酶抑制(ACEI)基础上加用1型血管紧张素II受体阻滞剂(ARB)可进一步减轻左心室(LV)重构。我们假设,ACEI与ARB联合治疗(CT)在限制重构过程中未治疗的相邻非梗死区域发生的心肌细胞肥大和功能障碍方面具有相加作用。

方法与结果

19只绵羊接受冠状动脉结扎以造成中等大小的前壁心尖梗死。心肌梗死后第2天,绵羊被随机分为接受雷米普利治疗(ACEI组,n = 5)或雷米普利加氯沙坦治疗(CT组,n = 6)或不治疗(未治疗组,n = 8)。各组梗死面积相似。心肌梗死后8周,从梗死周边和远离梗死的区域分离心肌细胞,测量形态学指标(细胞体积、长度、横截面积、宽度)以及收缩参数(缩短百分比和 -dL/dt,缩短速率)和舒张参数(+dL/dt [再伸长速率] 和TR 70% [70%再伸长时间])。测量相邻和远离区域的胶原容积百分比。各组相邻心肌细胞体积不同(CT组为2.5±0.1×10⁴立方微米,ACEI组为3.0±0.4×10⁴立方微米,未治疗组为3.5±0.2×10⁴立方微米,方差分析[ANOVA] P = 0.001),长度也不同(分别为158±4微米、161±9微米、189±8微米,ANOVA P < 0.001)。CT组相邻细胞体积和长度低于未治疗组(P < 0.05)。与未治疗相比,ACEI(7.9±0.3%,-131±6微米/秒,P < 0.05)和CT(7.7±0.3%,-144±8微米/秒,P < 0.05)均可改善分离的相邻心肌细胞的缩短百分比和 -dL/dt以及 +dL/dt和TR 70%。相邻或远离区域的胶原容积百分比在各组间未发现差异。

结论

与单独使用ACEI相比,加用ARB可在心肌梗死后左心室重构期间进一步限制相邻非梗死心肌细胞肥大。单独使用ACEI和CT均可保留分离的无负荷心肌细胞功能,但均未显著减少间质胶原。ARB对体内局部和整体功能的额外益处可能也归因于其他因素,包括局部负荷。

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