Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P01185 (vasopressin)
 23,126 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Tumors of the female genital tract may be associated with a variety of unusual clinical manifestations. Uncommon endocrine and paraendocrine syndromes include production of human chorionic gonadotropin by tumors other than those of germ cell origin, hyperthyroidism associated with struma ovarii and gestational trophoblastic disease, the carcinoid syndrome, the Zollinger-Ellison syndrome, hypercalcemia, Cushing's syndrome, hypoglycemia, hypertension related to renin or aldosterone production, hyperprolactinemia, inappropriate secretion of antidiuretic hormone, and virilization associated with Nelson's syndrome and placental site trophoblastic tumor. Paraneoplastic syndromes associated with gynecological tumors include disorders of the nervous system, connective tissue, and skin, as well as hematologic abnormalities and the nephrotic syndrome. Heritable and other congenital syndromes associated with these tumors are the Peutz-Jeghers syndrome, the nevoid basal-cell carcinoma syndrome, Ollier's disease and Maffucci's syndrome, hereditary leiomyomatosis, ataxia-telangiectasia, von Hippel-Lindau's disease, thyroid abnormalities associated with Sertoli-Leydig cell tumors, and Carney's complex. Other syndromes associated with tumors of the female genital tract include Meigs' syndrome, hyperamylasemia, uveal melanocytic lesions, and pyrexia.
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PMID:Clinical syndromes associated with tumors of the female genital tract. 175 57

Serum growth hormone (GH) levels were measured in 3 brothers with Hunter syndrome. The secretion of GH was studied by means of insulin (ITT), glucose (GTT), lysine-vasopressin (LVP), and L-Dopa administrations. Mean basal GH levels during the 4 tests were high (x = 14.2 ng/ml) in all cases. In the ITT and LVP tests, GH responses correlated positively with the patients' ages. Contrarily, after L-Dopa administration, GH elevations were normal in the two younger and absent in the oldest case. During GTT, GH levels were suppressed in all cases as expected. Basal cortisol and prolactin serum levels during the tests were normal. In order to clarify these data, GH levels were then determined during 120 min. (20-20 min.) under basal conditions. The means (+/- SD) of GH were 178 +/- 0.15; 4.42 +/- 2.47; and 2.30 +/- 0.71, for cases 1, 2 and 3, respectively (normal values 0-5 ng/ml). Basal somatomedin-C levels were in low-normal ranges. As patients were not undernourished and albumin levels were normal, a slight dysfunction of hypothalamic-pituitary-GH-somatomedin-C axis might occurred in these cases. The hypothesis here offered is that a primary sub-production of somatomedin-C, mainly by liver and kidneys, could be present in Hunter syndrome. This situation would lead to normal-high GH serum levels, as seen in the present cases. GH serum measurements in Hunter syndrome were not documented previously.
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PMID:[Serum growth hormone levels in Hunter's syndrome]. 184 6

To investigate pancreatic endocrine function in brain-dead patients, an intravenous glucose tolerance test (i.v. GTT) was performed in 8 brain-dead subjects maintained using the combined administration of vasopressin (ADH) and catecholamines during the first 3 days following the onset of brain death. Ten healthy adults served as control subjects. Although plasma glucose concentrations markedly increased and exceeded 300 mg/dl in most subjects just after the onset of brain death, they decreased to less than 200 mg/dl in most subjects after 24 h. The early insulin release also was significantly lower in brain dead subjects compared to controls (p < 0.01). The late insulin release was not decreased compared to controls but rather increased, which was accompanied by decreased glucose disappearance rate. The early insulin release recovered rapidly during the first 3 days following brain death without significant changes in the plasma hormone concentrations such as epinephrine, human growth hormone, thyroid-stimulating hormone, triiodothyronine, thyroxine, cortisol, and glucagon. The early insulin release and the plasma glucose concentration just before i.v. GTT was negatively correlated (R = -0.55, p < 0.05). We suggest awaiting recovery from hyperglycemia and early insulin release provides a reasonable approach to transplantation of the pancreas.
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PMID:Transient suppression of pancreatic endocrine function in patients following brain death. 865 94