Bishop C M, McCabe C J, Gittoes N J, Butler P J, Franklyn J A
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
J Endocrinol. 2000 Jun;165(3):607-15. doi: 10.1677/joe.0.1650607.
Skeletal muscles are important target tissues for thyroid hormone action. The present study examines the influence of thyroid status on muscle growth and tissue-specific expression of thyroid receptor (TR) mRNA isoforms in a commercial strain of the domestic duck (Anas platyrhynchos). Four groups (n=5) of 1-week-old ducklings were rendered either hypothyroid by treatment with methimazole (6 mg 100 g(-1) body mass or 12 mg 100 g(-1) body mass), or hyperthyroid by treatment with methimazole (6 mg 100 g(-1) body mass) in combination with thyroid hormones (5 microg thyroxine (T(4)) and tri-iodothyronine (T(3)) 100 g(-1) body mass or 10 microg T(4) and T(3) 100 g(-1) body mass). Serum and tissue samples (cardiac, pectoralis and semimembranosus leg muscle, liver, pituitary and cerebral cortex) were collected from these four groups, and from a group of untreated controls, at 8 weeks of age. Development of duckling morphology was retarded in methimazole-treated birds compared with that in euthyroid controls, as evidenced by differences in skeletal dimensions, primary feather length, and body and muscle masses. Body mass was lower by 18%, and relative masses of cardiac and pectoralis muscles were lower by 28% and 32% respectively. Heterologous oligonucleotides for TR alpha, TR beta 0, TR beta2 and the housekeeping gene beta-actin were derived from chicken sequences. RT-PCR showed that TR alpha mRNA was expressed in all tissues but was not significantly affected by any of the experimental treatments. TR beta 0 mRNA expression was significantly lower in the leg muscles of ducklings treated with 12 mg methimazole 100 g(-1) body mass (0.109+/-0.047 TR:beta-actin ratio, P<0.05) compared with that in euthyroid controls (0.380+/-0.202), but was unaltered in the pectoralis and cardiac muscles. Expression of TR beta 0 mRNA was significantly higher in pectoralis (by 3.5-fold, P<0. 05), cardiac (by 4.2-fold, P=0.003) and leg (by 4.0-fold, P<0.001) muscles of ducklings treated with thyroid hormones compared with those in euthyroid controls (0.098+/-0.019, 0.822+/-0.297 and 0. 38+/-0.202 TR:beta-actin respectively). Only the pituitary gland expressed significant levels of TR beta 2 mRNA.
骨骼肌是甲状腺激素作用的重要靶组织。本研究检测了甲状腺状态对家鸭(绿头鸭)一个商业品系肌肉生长及甲状腺受体(TR)mRNA亚型组织特异性表达的影响。将4组(每组n = 5)1周龄雏鸭通过用甲巯咪唑(6 mg/100 g体重或12 mg/100 g体重)处理使其甲状腺功能减退,或通过用甲巯咪唑(6 mg/100 g体重)联合甲状腺激素(5 μg甲状腺素(T4)和三碘甲状腺原氨酸(T3)/100 g体重或10 μg T4和T3/100 g体重)处理使其甲状腺功能亢进。在8周龄时,从这4组以及一组未处理的对照雏鸭中采集血清和组织样本(心脏、胸肌和半膜肌腿部肌肉、肝脏、垂体和大脑皮层)。与甲状腺功能正常的对照雏鸭相比,用甲巯咪唑处理的雏鸭形态发育受阻,这可通过骨骼尺寸、初级羽毛长度以及体重和肌肉质量的差异得以证明。体重降低了18%,心脏和胸肌的相对质量分别降低了28%和32%。TRα、TRβ0、TRβ2和管家基因β-肌动蛋白的异源寡核苷酸来源于鸡的序列。逆转录聚合酶链反应(RT-PCR)显示,TRα mRNA在所有组织中均有表达,但不受任何实验处理的显著影响。与甲状腺功能正常的对照雏鸭(TR:β-肌动蛋白比值为0.380±0.202)相比,用12 mg/100 g体重甲巯咪唑处理的雏鸭腿部肌肉中TRβ0 mRNA表达显著降低(TR:β-肌动蛋白比值为0.109±0.047,P<0.05),但胸肌和心脏肌肉中的表达未改变。与甲状腺功能正常的对照雏鸭(TR:β-肌动蛋白比值分别为0.098±0.019、0.822±0.297和0.38±0.202)相比,用甲状腺激素处理的雏鸭胸肌(升高3.5倍,P<0.05)、心脏(升高4.2倍,P = 0.003)和腿部(升高4.0倍,P<0.001)肌肉中TRβ0 mRNA表达显著升高。只有垂体表达显著水平的TRβ2 mRNA。