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地塞米松诱导的仔猪生长和骨代谢异常可被生长激素部分减弱,胰岛素样生长因子-I无协同作用。

Dexamethasone-induced abnormalities in growth and bone metabolism in piglets are partially attenuated by growth hormone with no synergistic effect of insulin-like growth factor-I.

作者信息

Ward W E, Donovan S M, Atkinson S A

机构信息

Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.

出版信息

Pediatr Res. 1998 Aug;44(2):215-21. doi: 10.1203/00006450-199808000-00013.

DOI:10.1203/00006450-199808000-00013
PMID:9702917
Abstract

Dexamethasone (DEX) therapy improves pulmonary compliance in premature infants with chronic lung disease; however, normal growth and bone development are impaired. Because DEX may mediate its effects by altering the GH-IGF-I axis, we investigated whether adjunctive therapy with GH or GH + IGF-I during DEX therapy could attenuate these DEX-induced effects. Piglets were randomized to placebo, oral tapered DEX (0.5, 0.3, and 0.2 mg kg(-1) d(-1) over 14 d), DEX + GH (0.1 mg kg(-1) d(-1)) or DEX + GH + IGF-I (0.1 mg kg(-1) d(-1)). Final whole body weight and length were improved with GH or GH + IGF-I compared with the DEX alone group. Plasma GH and IGF-I were not influenced by DEX, but infusion of IGF-I resulted in higher (p < 0.05) plasma IGF-I compared with all other groups at d 15. DEX reduced (p < 0.05) circulating IGFBP-2 and IGFBP-3 and liver IGFBP-2 and IGFBP-4 mRNA expression compared with controls. Treatment with DEX alone resulted in lower (p < 0.05) plasma osteocalcin, urinary N-telopeptide, and whole body and femur bone mineral density compared with controls, whereas results with piglets receiving adjunctive GH or GH + IGF-I were similar to those of controls. Given adjunctively, GH alone appears to partially counter the abnormalities in growth and bone metabolism associated with DEX therapy; however, this improvement cannot be attributed to higher circulating IGF-I, because combined therapy did not further improve growth or bone homeostasis compared with DEX + GH treatment. Growth hormone therapy has the potential to stimulate growth in infants exposed to steroid treatment.

摘要

地塞米松(DEX)治疗可改善患有慢性肺病的早产儿的肺顺应性;然而,其正常生长和骨骼发育会受到损害。由于DEX可能通过改变生长激素-胰岛素样生长因子-I(GH-IGF-I)轴来介导其作用,我们研究了在DEX治疗期间联合使用GH或GH + IGF-I治疗是否可以减轻这些DEX诱导的影响。将仔猪随机分为安慰剂组、口服递减剂量DEX组(14天内分别为0.5、0.3和0.2 mg kg⁻¹ d⁻¹)、DEX + GH组(0.1 mg kg⁻¹ d⁻¹)或DEX + GH + IGF-I组(0.1 mg kg⁻¹ d⁻¹)。与单独使用DEX组相比,GH或GH + IGF-I可改善最终的全身体重和体长。血浆GH和IGF-I不受DEX影响,但在第15天时,与所有其他组相比,输注IGF-I导致血浆IGF-I更高(p < 0.05)。与对照组相比,DEX降低了(p < 0.05)循环中的IGFBP-2和IGFBP-3以及肝脏IGFBP-2和IGFBP-4 mRNA表达。与对照组相比,单独使用DEX治疗导致血浆骨钙素、尿N-端肽以及全身和股骨骨矿物质密度更低(p < 0.05),而接受联合GH或GH + IGF-I治疗的仔猪的结果与对照组相似。单独联合使用GH似乎可以部分对抗与DEX治疗相关的生长和骨代谢异常;然而,这种改善不能归因于更高的循环IGF-I,因为与DEX + GH治疗相比,联合治疗并未进一步改善生长或骨内环境稳定。生长激素治疗有可能刺激接受类固醇治疗的婴儿的生长。

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