Anorexia nervosa e transtorno alimentar não especificado (TANE) são os transtornos alimentares mais frequentes na adolescência. Cursam com alterações hormonais e amenorreia. Este projeto tem como objetivo a maior compreensão das alterações laboratoriais e hormonais que ocorrem concomitantemente com esses transtornos alimentares na adolescência, em especial a relação com o retorno dos ciclos menstruais, a recuperação nutricional e a secreção de leptina e IGF-1. Vinte e oito adolescentes do sexo feminino, portadoras de anorexia nervosa ou TANE foram submetidas a coletas de amostras de sangue para dosagem de leptina, LH, FSH, PRL, estradiol, GH, IGF-1, TSH, T4L, T4, T3, proteínas totais e frações, função renal, hemograma, ferro, ferritina e eletrólitos no início do estudo e a cada cinco semanas num total de cinco coletas. Densitometria óssea foi realizada no início do acompanhamento e após seis meses para avaliar comprometimento ósseo. As principais complicações clínicas observadas foram amenorreia (78%) e osteoporose (14,8%). No início do estudo, 12 pacientes encontravam-se desnutridas com z score de IMC -2. As alterações hormonais presentes foram: diminuição do T3, estradiol, leptina, LH e IGF-1. As pacientes evoluíram com boa recuperação nutricional (variação da média de IMC ao longo do estudo IMC p < 0,01) e melhora dos parâmetros clínicos e hormonais. O IGF-1 apresentou-se como o melhor marcador de recuperação nutricional (p = 0,0001) e teve boa correlação com o retorno menstrual. À época do retorno menstrual as pacientes apresentaram IGF-1 > 340ng/mL (p = 0,04) / Anorexia Nervosa (AN) and eating disorder not otherwise specified (EDNOS) are the most frequent eating disorders in adolescence. The patients show hormonal alterations as well as amenorrhea. The aim of this study was to improve the knowledge of hormonal disturbances that occur together with AN and EDNOS, especially with regard to menstrual cycles, nutritional recovery as well as leptin and IGF-1 secretion. Twenty eight female adolescents with AN or EDNOS had blood collected for the following dosages: leptin, LH, FSH, PRL, estradiol, GH, IGF-1, TSH, FT4, T4, T3, total proteins and fractions, renal function, CBC, iron , ferritin, electrolytes in the beginning of the study and at every 5 weeks totalizing 5 samples per patient. Bone densitometry was performed at the start and after 6 months. The main clinical complications were amenorrhea (78%) and osteoporosis (14.8%). Twelve patients were undernourished at the start of the study (BMI z score = -2). Hormonal alterations were low T3, estradiol, leptina, LH, and IGF-1. The patients had good nutritional recovery, evaluated as a variation of BMI (p < 0.001) and improved clinical and hormonal parameters. IGF-I was the best marker of nutritional recovery (p = 0.0001) and correlated very well with menstrual cycles recovery. At the time when the patients resumed menstrual cycles, IGF-1 was above 340ng/mL (p = 0.04)

Leishmaniose visceral (LV) é uma doença causada pelo protozoário Leishmania (Leishmania) infantum nas Américas que acomete células do sistema fagocítico mononuclear. Na doença ativa, ocorre redução nos níveis de lipoproteínas de alta densidade (HDL) e aumento nos níveis de colesterol total e triglicérides, sendo que a progressão da doença pode estar relacionada com essas alterações no nível de lipoproteínas. Desta forma, neste trabalho avaliamos: o efeito das lipoproteínas de muita baixa densidade (VLDL) e HDL no parasitismo de células de linhagem monocítica humana (THP-1) por L. (L.) infantum, a atividade da arginase e a expressão do mRNA do fator de crescimento insulina símile-I (\"insulin-like growth factor-I\" = IGF-I) e seu receptor (\"insulin-like growth factor-I receptor\" = IGF-IR). Células THP-1 foram infectadas por 6 h com promastigotas de L. (L.) infantum, na presença de 0,5% de soro com baixa concentração lipídica (infranadante) e na presença ou ausência das frações lipoprotéicas em diferentes concentrações. As células foram lavadas e mantidas depois em meio de cultura acrescido com infranadante por 24, 48 e 72 h. Quando as frações de VLDL e HDL foram adicionadas separadamente durante a incubação inicial o parasitismo aumentou em relação ao controle. Quando as frações de VLDL e HDL foram adicionadas concomitantemente houve diminuição do parasitismo em relação ao controle, mas aumento inesperado da atividade da arginase, nos períodos de 24 e 48 h. A expressão do mRNA de IGF-I e IGF-IR mostrou uma diminuição nas células infectadas na presença e ausência das frações em relação às células não infectadas. Os resultados obtidos sugerem um papel importante de VLDL e HDL na infecção de células THP-1 por L. (L.) infantum. / Visceral leishmaniasis (VL) is a disease caused by the protozoan Leishmania (Leishmania) infantum in Americas that affects cells of the mononuclear phagocytic system. During active disease reduction in high density lipoprotein (HDL) and increase in total cholesterol and triglyceride levels are observed. Thus in this study we evaluated the effect of very low density lipoprotein (VLDL) and HDL on the parasitism of cells of human monocytic line (THP-1) by L. (L.) infantum, the arginase activity and insulin-like growth factor-I (IGF-I) and insulin-like growth factor-I receptor (IGF-IR) mRNA expressions. THP-1 cells were infected for 6 h with L. (L.) infantum promastigotes in the presence of 0.5% low lipid concentration serum (infranatant) in the presence or absence of lipoprotein fractions at different concentrations. The cells were washed and then maintained in medium with infranatant for 24, 48 and 72 h. When VLDL and HDL were added separately the parasitism increased when compared with the control. When VLDL and HDL were added concomitantly the parasitism decreased in relation to the control but with unexpected increase in arginase activity. The evaluation of IGF-I and IGF-IR mRNA expression showed a decrease in the cells infected in the presence and absence of the fractions comparing with the uninfected cells. The results suggest an important effect of VLDL and HDL in the infection of THP-1 cells by L. (L.) infantum.

This study examined if multi-joint resistance exercises could elicit expression of biomarkers associated with neuroprotection. Thirteen well-trained males performed 4 sets to failure at 80% of a one-repetition maximum (1RM) on the back squat, bench press, and deadlift. The biomarkers measured immediately pre- and post-exercise were brain derived neurotrophic factor (BDNF), insulin-like growth factor 1 (IGF-1), cathepsin B (CatB), and interleukin 6 (IL-6). There was a main time effect (p<0.01) for BDNF with significant increases in the deadlift (p=0.01) and bench press (p=0.01) conditions, but not the squat (p=0.21). There was a main time effect (p<0.01) for IL-6 with a significant increase in the squat (p<0.01). There was no significant increase in CatB or IGF-1 (p>0.05). Additionally, there was no significant relationship between BDNF and IL-6 response. / Includes bibliography. / Thesis (M.S.)--Florida Atlantic University, 2019. / FAU Electronic Theses and Dissertations Collection

Includes bibliographical references (leaves 159-213) Shows that IGF-I peptides are effective in diminishing post-surgical catabolism and enhancing adaptive gut hyperplasia in rats recovering from massive small bowel resection.

Includes bibliographical references (leaves 188-217) Insulin-like growth factor-I circulates at high concentrations in blood, mainly complexed with IGF-binding proteins. The main objective of the thesis is to determine the general role played by plasma IGF-binding proteins in the regulation of IGF transfer from blood to tissues.

xxiii, 222 leaves : ill., plates ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Shows that IGF-I peptides are effective in diminishing post-surgical catabolism and enhancing adaptive gut hyperplasia in rats recovering from massive small bowel resection. / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Science, 1992

Thesis (Ph. D.)--University of Washington, 2006. / Vita. Includes bibliographical references (leaves 44-53).

Thesis (Ph. D.)--University of Washington, 2001. / Vita. Includes bibliographical references (leaves 96-116).

Thesis (Ph. D.)--University of Washington, 2003. / Vita. Includes bibliographical references (leaves 79-87).

Mesenchymal stromal cells (MSC) are bone marrow-derived, non-hematopoietic progenitors that are amenable to genetic engineering, making them attractive delivery vehicles for therapeutic proteins. However, limited transplanted cell survival compromises the efficacy of MSC-based gene therapy. We hypothesized that co-implantation of insulin-like growth factor-1 (IGF-I)-overexpressing MSC (MSC-IGF) would improve MSC-based therapy of anemia by providing paracrine support to erythropoietin (EPO)-secreting MSC (MSC-EPO). Murine MSC were found to express the IGF-I receptor and be responsive to IGF-I stimulation. IGF-I also improved MSC survival in vitro. MSC were admixed in a bovine collagen matrix and implanted by subcutaneous injection in a murine model of chronic renal failure. Mice receiving MSC-EPO co-implanted with MSC-IGF experienced a greater and significantly sustained elevation in hematocrit compared to controls; heart function was also improved. Co-implantation of MSC-IGF therefore represents a promising new strategy for enhancing implanted cell survival, and improving cell-based gene therapy of renal anemia.