Knehans A W, Romsos D R
Metabolism. 1984 Jul;33(7):652-7. doi: 10.1016/0026-0495(84)90065-9.
Thyroxine treatment improves some of the defective thermogenic properties of obese (ob/ob) mice. Because brown adipose tissue (BAT) is an important thermogenic organ in mice, effects of thyroxine treatment on Na+, K+-ATPase, a thyroid-hormone responsive enzyme, and on rates of norepinephrine (NE) turnover, an indicator of sympathetic nervous system activity, in BAT of lean and obese mice were evaluated. Female mice, six weeks old, were injected with approximately 4 micrograms thyroxine daily for 2 weeks. Numbers of Na+, K+-ATPase enzyme units in BAT were similar in control lean and obese mice. Thyroxine treatment increased numbers of Na+, K+-ATPase enzyme units by 60% and 100% in lean and obese mice, respectively, indicating that the BAT of obese mice was responsive to thyroxine treatment. Fractional rates of NE turnover were 75% faster in BAT of control lean mice than in obese mice. Thyroxine treatment decreased functional rates of NE turnover in BAT of lean mice by 35%, but had no effect on NE turnover in BAT of obese mice. Rates of NE turnover in heart and pancreas of control lean and obese mice were unaffected by phenotype. Although the decreases in fractional rates of NE turnover in heart (-23%) and pancreas (-11%) of lean mice in response to thyroxine injections were not statistically significant, the calculated rates of NE turnover (fractional rate of NE turnover times the NE content of the organ) in these organs of lean mice were decreased 25% to 30% (P less than 0.05) in response to thyroxine. Thyroxine injections did not affect NE turnover in either heart or pancreas of obese mice.(ABSTRACT TRUNCATED AT 250 WORDS)
甲状腺素治疗可改善肥胖(ob/ob)小鼠一些有缺陷的产热特性。由于棕色脂肪组织(BAT)是小鼠体内重要的产热器官,因此评估了甲状腺素治疗对瘦小鼠和肥胖小鼠BAT中Na⁺,K⁺ - ATP酶(一种甲状腺激素反应性酶)以及去甲肾上腺素(NE)周转速率(交感神经系统活动的指标)的影响。六周龄雌性小鼠每天注射约4微克甲状腺素,持续2周。对照瘦小鼠和肥胖小鼠BAT中Na⁺,K⁺ - ATP酶单位数量相似。甲状腺素治疗使瘦小鼠和肥胖小鼠的Na⁺,K⁺ - ATP酶单位数量分别增加了60%和100%,表明肥胖小鼠的BAT对甲状腺素治疗有反应。对照瘦小鼠BAT中NE周转的分数速率比肥胖小鼠快75%。甲状腺素治疗使瘦小鼠BAT中NE周转的功能速率降低了35%,但对肥胖小鼠BAT中的NE周转没有影响。对照瘦小鼠和肥胖小鼠心脏和胰腺中的NE周转速率不受表型影响。尽管瘦小鼠心脏(-23%)和胰腺(-11%)中NE周转分数速率因注射甲状腺素而降低,但在统计学上并不显著,但瘦小鼠这些器官中计算出的NE周转速率(NE周转分数速率乘以器官中的NE含量)因甲状腺素而降低了25%至30%(P小于0.05)。甲状腺素注射对肥胖小鼠心脏或胰腺中的NE周转均无影响。(摘要截断于250字)