Interaction of hyperthyroidism and hindlimb suspension on skeletal myosin heavy chain expression

被引:43
作者
Haddad, F [1 ]
Qin, AX [1 ]
Zeng, M [1 ]
McCue, SA [1 ]
Baldwin, KM [1 ]
机构
[1] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92697 USA
关键词
slow myosin heavy chain; fast myosin heavy chains; messenger riboncleic acid; soleus; plantaris; vastus intermedius; Northern blot; 3,5,3 '-triiodothyronine;
D O I
10.1152/jappl.1998.85.6.2227
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We examined the novel interaction of hyperthyroidism and hindlimb suspension on the pattern of myosin heavy chain (MHC) expression (mRNA and protein) in skeletal muscles. Female Sprague-Dawley rats were assigned to four groups: I)normal control(Con); 2) thyroid hormone treated [150 mu g 3,5,3'-triiodothyronine (T-3).kg(-1).day(-1)] (T-3); 3) hindlimb suspension (HS); or 4) Ts-treated and HS (T-3 + HS). Results show for the first time the novel observation that the combination T-3 + HS induces a rapid and sustained, marked (80-90%) downregulation of type I MHC gene expression that is mirrored temporally by concomitant marked upregulation of type IIb MHC gene expression, as evidenced by the de novo synthesis of type IIb MHC protein in the soleus. The fast type IIx MHC isoform showed a differential response among the experimental groups, generally increasing with the separate and combined treatments in both the soleus and vastus intermedius muscles while decreasing in the plantaris muscles. The fast type IIa MHC was the least responsive to suspension of the MHCs and reflected its greatest responsiveness to Ts treatment while also undergoing differential adaptations in slow vs. fast muscle (increases vs. decreases, respectively). These results confirm previous findings that all four adult MHC genes are sensitive to Ts and suspension in a muscle-specific manner. In addition, we show that Tg + HS can interact synergistically to create novel adaptations in MHC expression that could not be observed when each factor was imposed separately.
引用
收藏
页码:2227 / 2236
页数:10
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