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N3im-甲基促甲状腺激素释放激素对人垂体-甲状腺轴的影响。

Effect of N3im-methyl-thyrotropin releasing hormone on the human pituitary-thyroid axis.

作者信息

Sowers J R, Hershman J M, Pekary A E, Nair M G, Baugh C M

出版信息

J Clin Endocrinol Metab. 1976 Oct;43(4):741-8. doi: 10.1210/jcem-43-4-741.

Abstract

The N3im-methyl analogue of thyrotropin release hormone (methyl-TRH) was compared with TRH as a thyrotropin releaser in 30 euthyroid volunteers (ages 19-61 years). The mean TSH response to 100 mug of methyl-TRH was greater (P less than 0.005) than the TSH response to 500 mug of TRH from 10 min to 240 min after giving the releasing factors. The mean peak TSH (at 30 min), maximum deltaTSH, and integrated TSH response area were greater (P less than 0.005) after administration of methyl-TRH than after TRH. The TSH response to methyl-TRH was significantly greater (P less than 0.05) for the 11 females than for the 19 males in this study. The mean baseline TSH was correlated with the maximum deltaTSH (r = 0.72, P less than 0.01) after methyl-TRH stimulation. The mean serum T3 concentration after methyl-TRH was significantly elevated at 60 min, peaked at 210 min and remained significantly elevated at 240 min. The peak serum T3, maximum T3 and T3 response area were significantly greater (P less than 0.005) after giving methyl-TRH than after TRH. The methyl-TRH induced T3 response area was 1.4 times the TRH induced T3 response area. The serum T4 concentration after methyl-TRH was elevated at 90 min (P less than 0.005), reached a peak at 210 min, and at 240 min was still 1.25 times the mean baseline T4. The peak serum T4, maximum deltaT4 and T4 response area after methyl-TRH were significantly greater than after TRH. The methyl-TRH induced T4 response area was 1.4 times the TRH induced T4 response area. The data indicate that methyl-TRH is a more potent thyrotropin releaser than TRH. Since N3im-methyl-histidine has been found in the brain, the possibility that this methyl analogue of TRH is a physiologic thyrotropin releaser should be evaluated.

摘要

在30名甲状腺功能正常的志愿者(年龄19 - 61岁)中,将促甲状腺激素释放激素的N3 - 亚氨基甲基类似物(甲基 - TRH)与TRH作为促甲状腺激素释放剂进行了比较。给予释放因子后10分钟至240分钟,100微克甲基 - TRH引起的促甲状腺激素(TSH)平均反应大于(P < 0.005)500微克TRH引起的TSH反应。给予甲基 - TRH后促甲状腺激素的平均峰值(30分钟时)、最大TSH变化量(deltaTSH)和TSH反应积分面积均大于(P < 0.005)给予TRH后。在本研究中,11名女性对甲基 - TRH的TSH反应显著大于(P < 0.05)19名男性。甲基 - TRH刺激后平均基础TSH与最大deltaTSH相关(r = 0.72,P < 0.01)。甲基 - TRH给药后,平均血清三碘甲状腺原氨酸(T3)浓度在60分钟时显著升高,在210分钟时达到峰值,并在240分钟时仍显著升高。给予甲基 - TRH后血清T3峰值、最大T3和T3反应面积均显著大于(P < 0.005)给予TRH后。甲基 - TRH诱导的T3反应面积是TRH诱导的T3反应面积的1.4倍。甲基 - TRH给药后血清甲状腺素(T4)浓度在90分钟时升高(P < 0.005),在210分钟时达到峰值,在24分钟时仍为平均基础T4的1.25倍。甲基 - TRH给药后的血清T4峰值、最大T4变化量(deltaT4)和T4反应面积均显著大于给予TRH后。甲基 - TRH诱导的T4反应面积是TRH诱导的T4反应面积的1.4倍。数据表明,甲基 - TRH是比TRH更有效的促甲状腺激素释放剂。由于在大脑中已发现N3 - 亚氨基甲基 - 组氨酸,因此应评估这种TRH的甲基类似物作为生理性促甲状腺激素释放剂的可能性。

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