Effects of Growth Hormone on Insulin Signal Transduction in Rat Adipose Tissue Maintained In Vitro

2004 ◽  
Vol 30 (2) ◽  
pp. 225-238 ◽  
Author(s):  
Fernanda C. P. Castro ◽  
Eduardo F. Delgado ◽  
Rosângela M. N. Bezerra ◽  
Dante P. D. Lanna
1997 ◽  
Vol 130 (1-2) ◽  
pp. 33-42 ◽  
Author(s):  
Ana C.P Thirone ◽  
Carla R.O Carvalho ◽  
Sigisfredo L Brenelli ◽  
Lı́cio A Velloso ◽  
Mario J.A. Saad

1960 ◽  
Vol 198 (3) ◽  
pp. 640-644 ◽  
Author(s):  
Rodney D. Orth ◽  
William D. Odell ◽  
Robert H. Williams

The effects of various hormones on the metabolism of acetate-i-C14 by rat adipose tissue in vitro were investigated. Using an albumin-containing medium, it was found that ACTH, growth hormone, epinephrine and glucagon each caused increased oxygen consumption, a decreased incorporation of acetate into tissue lipid, and an increase in the amount of newly synthesized lipid attached to albumin. The basic mechanism involved in the production of such qualitatively similar effects by each of the hormones studied are unknown.


2013 ◽  
Vol 217 (2) ◽  
pp. 131-140 ◽  
Author(s):  
Daniela F Bertelli ◽  
Andressa Coope ◽  
Andrea M Caricilli ◽  
Patricia O Prada ◽  
Mario J Saad ◽  
...  

The 72 kDa inositol polyphosphate 5-phosphatase E (72k-5ptase) controls signal transduction through the catalytic dephosphorylation of the 5-position of membrane-bound phosphoinositides. The reduction of 72k-5ptase expression in the hypothalamus results in improved hypothalamic insulin signal transduction and reduction of food intake and body mass. Here, we evaluated the tissue distribution and the impact of obesity on the expression of 72k-5ptase in peripheral tissues of experimental animals. In addition, insulin signal transduction and action were determined in an animal model of obesity and insulin resistance treated with an antisense (AS) oligonucleotide that reduces 72k-5ptase expression. In lean Wistar rats, 72k-5ptase mRNA and protein are found in highest levels in heart, skeletal muscle, and white adipose tissue. In three distinct models of obesity, Wistar rats, Swiss mice fed on high-fat diet, and leptin-deficient ob/ob mice, the expression of 72k-5ptase is increased in skeletal muscle and adipose tissue. The treatment of obese Wistar rats with an anti-72k-5ptase AS oligonucleotide results in significant reduction of 72k-5ptase catalytic activity, which is accompanied by reduced food intake and body mass and improved insulin signal transduction and action as determined by immunoblotting and clamp studies respectively. 72k-5ptase expression is increased in obesity and its AS inhibition resulted in a significant improvement in insulin signal transduction and restoration of glucose homeostasis.


2004 ◽  
Vol 449 (6) ◽  
pp. 537-546 ◽  
Author(s):  
Alessandra L. Gasparetti ◽  
Fernanda Alvarez-Rojas ◽  
Eliana P. de Araujo ◽  
Aparecida E. Hirata ◽  
Mário J. A. Saad ◽  
...  

1959 ◽  
Vol 234 (7) ◽  
pp. 1922-1928
Author(s):  
Albert I. Winegrad ◽  
Walter N. Shaw ◽  
Francis D.W. Lukens ◽  
William C. Stadie ◽  
Albert E. Renold

Endocrinology ◽  
1980 ◽  
Vol 107 (2) ◽  
pp. 538-544 ◽  
Author(s):  
BRUCE L. MALOFF ◽  
JOSEPH H. LEVINE ◽  
DEAN H. LOCKWOOD

2019 ◽  
Vol 243 (2) ◽  
pp. 97-110 ◽  
Author(s):  
Hong Ma ◽  
Jin Yuan ◽  
Jinyu Ma ◽  
Jie Ding ◽  
Weiwei Lin ◽  
...  

Bone morphogenetic protein 7 (BMP7), a member of the transforming growth factor-β (TGF-β) family, plays pivotal roles in energy expenditure. However, whether and how BMP7 regulates hepatic insulin sensitivity is still poorly understood. Here, we show that hepatic BMP7 expression is reduced in high-fat diet (HFD)-induced diabetic mice and palmitate (PA)-induced insulin-resistant HepG2 and AML12 cells. BMP7 improves insulin signaling pathway in insulin resistant hepatocytes. On the contrary, knockdown of BMP7 further impairs insulin signal transduction in PA-treated cells. Increased expression of BMP7 by adenovirus expressing BMP7 improves hyperglycemia, insulin sensitivity and insulin signal transduction. Furthermore, BMP7 inhibits mitogen-activated protein kinases (MAPKs) in both the liver of obese mice and PA-treated cells. In addition, inhibition of MAPKs recapitulates the effects of BMP7 on insulin signal transduction in cultured hepatocytes treated with PA. Activation of p38 MAPK abolishes the BMP7-mediated upregulation of insulin signal transduction both in vitro and in vivo. Together, our results show that hepatic BMP7 has a novel function in regulating insulin sensitivity through inhibition of MAPKs, thus providing new insights into treating insulin resistance-related disorders such as type 2 diabetes.


1962 ◽  
Vol 40 (6) ◽  
pp. 749-755 ◽  
Author(s):  
W. F. Perry ◽  
H. F. Bowen

The incubation of rat adipose tissue (epidymal fat) in the presence of growth hormone, ACTH, or epinephrine led to an increased production of non-esterified fatty acids (NEFA). The increased NEFA production induced by maximal concentration of the hormones was inhibited if insulin was also present in the medium but unaffected by the addition of glucose at a concentration of 300 mg%. Lower concentrations of growth hormone, however, were counteracted by this concentration of glucose.Adipose tissue from 72-hour fasted rats also exhibited increased NEFA production. Unlike the hormonally induced NEFA increase, the increase NEFA production by tissue from fasted animals was unaffected by insulin in the medium but was inhibited by the addition of glucose.


1962 ◽  
Vol 40 (1) ◽  
pp. 749-755 ◽  
Author(s):  
W. F. Perry ◽  
H. F. Bowen

The incubation of rat adipose tissue (epidymal fat) in the presence of growth hormone, ACTH, or epinephrine led to an increased production of non-esterified fatty acids (NEFA). The increased NEFA production induced by maximal concentration of the hormones was inhibited if insulin was also present in the medium but unaffected by the addition of glucose at a concentration of 300 mg%. Lower concentrations of growth hormone, however, were counteracted by this concentration of glucose.Adipose tissue from 72-hour fasted rats also exhibited increased NEFA production. Unlike the hormonally induced NEFA increase, the increase NEFA production by tissue from fasted animals was unaffected by insulin in the medium but was inhibited by the addition of glucose.


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