Growth Hormone Secretagogues as Potential Therapeutic Agents to Restore Growth Hormone Secretion in Older Subjects to Those Observed in Young Adults

被引:4
|
作者
Smith, Roy G. [1 ,2 ]
Thorner, Michael O. [3 ,4 ,5 ]
机构
[1] Scripps Res Inst, Dept Mol Med, La Jolla, CA USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX USA
[3] Univ Virginia, Dept Med, Charlottesville, VA USA
[4] Lumos Pharm, Austin, TX USA
[5] Lumos Pharm Inc, 4200 Marathon Blvd, Suite 200, Austin, TX 78756 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2023年 / 78卷
基金
美国国家卫生研究院;
关键词
Functional limitation; Growth hormone secretagogues; Skeletal muscle dysfunction; Mobility disability; Sarcopenia; BONE TURNOVER; GHRELIN; PITUITARY; RELEASE; MK-677; INCREASES; HEALTHY; MARKERS;
D O I
10.1093/gerona/glad022
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The discovery of the growth hormone secretagogues (GHS) and the reverse pharmacology leading to the discovery of GHS receptor which enabled the identification of ghrelin as the natural ligand for the receptor have opened a new horizon in growth hormone (GH) physiology, pathophysiology, and therapeutics. Major progress has been made and we now have orally active GHS which are able to restore optimal pulsatile GH secretion which cannot be overstimulated as insulin-like growth factor feedback regulates the peaks to the optimum level. This enables GH to be restored in the older to levels normally seen in 20- to 30-year-old people; this leads to an increase in fat-free mass and redistribution of fat to the limbs. As these agents are ultimately approved and investigated further, it is likely that they will be shown to restore growth in children with moderate-to-mild GH deficiency; their benefits will be investigated in other indications such as nonalcoholic fatty liver disease, frailty, anemia, osteoporosis, and immune compromise in older subjects. The exquisite regulation of GH secretion reflects the importance of GH pulsatility in the regulation of somatotroph action of GH.
引用
收藏
页码:S38 / S43
页数:6
相关论文
共 25 条
  • [21] Administration of ghrelin to young uraemic rats increases food intake transiently, stimulates growth hormone secretion and does not improve longitudinal growth
    Alvarez-Garcia, Oscar
    Garcia-Lopez, Enrique
    Rodriguez, Julian
    Gil-Pena, Helena
    Molinos, Ines
    Carbajo-Perez, Eduardo
    Santos, Fernando
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (05) : 1309 - 1313
  • [22] Maturation of the regulation of growth hormone secretion in young males with hypogonadotropic hypogonadism pharmacologically exposed to progressive increments in serum testosterone
    Giustina, A
    Scalvini, T
    Tassi, C
    Desenzani, P
    Poiesi, C
    Wehrenberg, WB
    Rogol, AD
    Veldhuis, JD
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) : 1210 - 1219
  • [23] Age-Dependent Decline in Acyl-Ghrelin Concentrations and Reduced Association of Acyl-Ghrelin and Growth Hormone in Healthy Older Adults
    Nass, Ralf
    Farhy, Leon S.
    Liu, Jianhua
    Pezzoli, Suzan S.
    Johnson, Michael L.
    Gaylinn, Bruce D.
    Thorner, Michael O.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (02) : 602 - 608
  • [24] Clinical characteristics, timing of peak responses and safety aspects of two dosing regimens of the glucagon stimulation test in evaluating growth hormone and cortisol secretion in adults
    Yuen, Kevin C. J.
    Biller, Beverly M. K.
    Katznelson, Laurence
    Rhoads, Sharon A.
    Gurel, Michelle H.
    Chu, Olivia
    Corazzini, Valentina
    Spiller, Kellie
    Gordon, Murray B.
    Salvatori, Roberto
    Cook, David M.
    PITUITARY, 2013, 16 (02) : 220 - 230
  • [25] Addition of recombinant follicle-stimulating hormone to human chorionic gonadotropin treatment in adolescents and young adults with hypogonadotropic hypogonadism promotes normal testicular growth and may promote early spermatogenesis
    Zacharin, Margaret
    Sabin, Matthew A.
    Nair, Veena V.
    Dagabdhao, Preeti
    FERTILITY AND STERILITY, 2012, 98 (04) : 836 - 842