Gertz B J, Sciberras D G, Yogendran L, Christie K, Bador K, Krupa D, Wittreich J M, James I
Merck Research Laboratories, Rahway, New Jersey 07065-0914.
J Clin Endocrinol Metab. 1994 Sep;79(3):745-9. doi: 10.1210/jcem.79.3.8077355.
The reversal of glucocorticoid-induced negative nitrogen balance by GH supports a possible therapeutic role for GH treatment in patients receiving these catabolic steroids. A GH secretagogue might be of similar utility. However, stimulated GH secretion is generally suppressed by glucocorticoids. To test whether L-692,429, a nonpeptide mimic of GH-releasing peptide-6, can overcome such suppression, a double blind, placebo-controlled, three-period, cross-over study was performed in nine healthy young men who received 0.2 mg/kg L-692,429, i.v., preceded by 4 days of prednisolone (20 mg, orally, three times daily) or placebo, and 0.75 mg/kg L-692,429 preceded by prednisolone only. The mean (SE) GH peak and area under the curve between 0-240 min after administration of 0.2 mg/kg L-692,429 in the absence of steroid were 53.8 (7.2) micrograms/L and 3481 (1005) micrograms/min.L, which were reduced to 25.1 (3.4) micrograms/L and 1342 (285) micrograms/min.L (P < or = 0.01) when treatment was preceded by 4 days of prednisolone. However, the suppressive influence of the steroid was attenuated by the high dose of L-692,429, which achieved a GH peak and area under the curve between 0-240 min of 42.6 (5.8) micrograms/L and 2298 (425) micrograms/min.L, respectively (P < 0.01 vs. 0.2 mg/kg L-692,429 plus prednisolone). L-692,429 stimulates GH secretion even in the setting of short term, high dose, concomitant glucocorticoid treatment, suggesting that such compounds might provide an alternative means of increasing circulating GH and reversing the catabolic effects of these steroids.
生长激素(GH)可逆转糖皮质激素诱导的负氮平衡,这表明GH治疗对于接受这些分解代谢类固醇治疗的患者可能具有治疗作用。生长激素促分泌素可能具有类似的效用。然而,糖皮质激素通常会抑制GH的分泌。为了测试生长激素释放肽-6的非肽模拟物L-692,429是否能克服这种抑制作用,对9名健康年轻男性进行了一项双盲、安慰剂对照、三阶段交叉研究。这些男性先接受4天的泼尼松龙(20mg,口服,每日三次)或安慰剂治疗,然后静脉注射0.2mg/kg的L-692,429,或者仅在接受泼尼松龙治疗后静脉注射0.75mg/kg的L-692,429。在无类固醇的情况下,静脉注射0.2mg/kg的L-692,429后0至240分钟内,GH的平均(SE)峰值和曲线下面积分别为53.8(7.2)μg/L和3481(1005)μg/min·L;当在4天的泼尼松龙治疗后进行同样的处理时,GH峰值和曲线下面积分别降至25.1(3.4)μg/L和1342(285)μg/min·L(P≤0.01)。然而,高剂量的L-692,429减弱了类固醇的抑制作用,其在0至240分钟内的GH峰值和曲线下面积分别达到42.6(5.8)μg/L和2298(425)μg/min·L(与0.2mg/kg的L-692,429加泼尼松龙相比,P<0.01)。即使在短期、高剂量、同时使用糖皮质激素治疗的情况下,L-692,429仍能刺激GH分泌,这表明此类化合物可能为增加循环GH水平和逆转这些类固醇的分解代谢作用提供一种替代方法。