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Query: UMLS:C0001430 (
adenoma
)
21,222
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We measured the amount of binding sites for
endothelin-1
(
ET-1
) in the bladder and prostate in patients with and without benign prostatic hypertrophy (PH and NPH group) using 125I-
ET-1
. Also the localization of
ET-1
binding sites in hypertrophied
adenoma
was studied using autoradiography. Saturation experiments with 125I-
ET-1
revealed that there were single class of saturable high affinity binding sites for 125I-
ET-1
in the homogenate of the bladder (dome and base) and prostate (
adenoma
and capsule). The KD values to the bladder and prostate were not different between PH and NPH group. The Bmax values in the bladder (base and dome) were significantly lower in the PH group. While those in the prostate (
adenoma
and capsule) were significantly higher in the PH group. Autoradiograms of hypertrophied
adenoma
showed that
ET-1
binding sites were localized to the stromal smooth muscles as well as to the glandular epithelium. These data suggest that ETs affect the pathophysiology of BPH through the changes in receptor density in both the bladder and prostate.
...
PMID:[Effect of benign prostatic hypertrophy on the endothelin-1 receptor density in human urinary bladder and prostate]. 750 57
This study evaluated the assessment of plasma
endothelin-1
(
ET-1
) levels in primary aldosteronism and its correlation with other vasoactive hormones such as renin, aldosterone, catecholamines, arginine-vasopressin, and atrial natriuretic peptide. Plasma
ET-1
was measured in 12 patients with primary aldosteronism (five adenomas and seven primary hyperplasia) and in 15 normal subjects. No significant differences were found in plasma
ET-1
between controls and hypertensive patients both in
adenoma
and primary adrenal hyperplasia (8.8 + 1.6 pg/mL v 6.2 + 1.4 pg/mL v 6.5 + 1.0 pg/mL, P = NS, respectively). Further, no significant correlations were found among
ET-1
and vasoactive hormones. In conclusion, these findings show that there are no differences in
ET-1
levels between primary aldosteronism patients and healthy subjects. Circulating
ET-1
is not involved in the hypertension in primary aldosteronism.
...
PMID:Plasma immunoreactive endothelin-1 in primary hyperaldosteronism. 791 56
Compelling evidence indicates that the endothelium-derived potent vasoconstrictor
endothelin-1
(
ET-1
) stimulates aldosterone secretion by interacting with specific receptors. Although two different
ET-1
receptors have been identified and cloned, the receptor subtype involved in mediating aldosterone secretion is still unknown. Accordingly, we wished to investigate whether the genes of
ET-1
and of its receptors A and B are expressed in the normal human adrenal cortex. We designed specific primers for
ET-1
and the ETA and ETB receptors genes and developed a reverse transcription polymerase chain reaction (RT-PCR) with chemiluminescent quantitation of the cDNA. In addition, we carried out 125I
ET-1
displacement studies with cold
ET-1
, ET-3 and the specific ETA and ETB ligands BQ123 and sarafotoxin 6C. Localization of each receptor subtype was also investigated by autoradiography. Binding experiments were first individually analyzed by Scatchard and Hofstee plot and then coanalyzed by the nonlinear iterative curve fitting program Ligand. Histologically normal adrenal cortex tissue, obtained from kidney cancer patients (n = 7), and an aldosterone-producing
adenoma
(APA), which is histogenetically derived from the zona glomerulosa (ZG) cells, were studied. Results showed that the
ET-1
, ETA and ETB mRNA can be detected by RT-PCR in all adrenal cortices as well as in the APA. The best fitting of the 125I
ET-1
displacement binding data was consistently provided by a two-site model both in the normal adrenal cortex (F = 22.1, P < 0.0001) and in the APA (F = 18.4, P < 0.0001). In the former the density (Bmax) of the ETA and ETB subtype was 2.6 +/- 0.5 pmol/mg protein (m +/- SEM) and 1.19 +/- 0.6, respectively. The dissociation constant (Kd) of
ET-1
, ET-3, S6C, and BQ-123 for each receptor subtype resulted to be within the range reported for human tissue for the ETA and ETB receptors. In the APA tissue the Bmax tended to be lower (1.33 and 0.8 pmol/mg protein, for the ETA and ETB, respectively) but the Kd were similar. Autoradiographic studies confirmed the presence of both receptor subtypes on the ZG as well as on APA cells. Thus, the genes of
ET-1
and both its receptor subtypes ETA and ETB are actively transcribed in the human adrenal cortex. Furthermore, both receptor subtypes are translated into proteins in ZG and APA cells.
...
PMID:Gene expression, localization, and characterization of endothelin A and B receptors in the human adrenal cortex. 808 64
The aim of the study was to evaluate possible changes of plasma
endothelin-1
levels (ET-1) in patients with hypertension secondary to primary aldosteronism and pheochromocytoma. We enrolled in the study: 12 patients affected by aldosterone-producing
adenoma
(5 M and 7 W; mean age 42.1 +/- 17.2 years); 8 patients with pheochromocytoma (5 M, 3 W; mean age 36.2 +/- 17.1 years); 15 patients with essential hypertension (9 M, 6 W; mean age 48.5 +/- 10 years). We also enrolled a normal control group (8 M, 12 W; mean age 34.2 +/- 11 years). The mean plasma ET-1 concentrations in patients with pheochromocytoma were significantly higher (23.9 +/- 5.2 pg/ml) than those in normal subjects (7.3 +/- 1.9 pg/ml), in patients with primary aldosteronism (12.1 +/- 3.8 pg/ml) and in patients with essential hypertension (9.2 +/- 3 pg/ml); p < 0.001, respectively. The present investigation demonstrates that in human adrenal hypertension patients with pheochromocytoma have increased circulating ET-1 levels respect to patients with aldosterone-producing
adenoma
.
...
PMID:Plasma endothelin-1 levels in patients with aldosterone-producing adenoma and pheochromocytoma. 888 76
To elucidate the pathophysiologic significance of
endothelin-1
(
ET-1
) in adrenal and the mechanism for reduced responsiveness to exogenous
ET-1
in aldosterone-producing
adenoma
(APA), we have investigated
ET-1
receptors by radioligand binding assay (RBA) in human normal adrenal (NA), APA, idiopathic hyperaldosteronism (IHA), and pheochromocytoma (PHEO), immunoreactive (ir-)
ET-1
content in NA, APA and PHEO by radioimmunoassay (RIA), and immunohistochemical staining of
ET-1
with the peroxidase-anti-peroxidase (PAP) method in NA, APA, and PHEO. A single class of high-affinity binding sites for
ET-1
was found in human NA and tumor tissues. Dissociation constant (Kd) values of
ET-1
receptors were similar in NA, APA, and IHA, but maximal binding capacity (Bmax) of
ET-1
receptors was lower in APA than in NA and IHA. Both Kd and Bmax in PHEO were higher than those in NA, APA, and IHA. Ir-
ET-1
content in tumors of APA and PHEO were higher than in NA. Immunohistochemical staining was more intense in the tumor cells of APA and PHEO than in NA. These results suggest that the reduced response to exogenous
ET-1
in APA could be related to downregulation of
ET-1
receptors in the tumor. Increased
ET-1
content and receptors may lead to hypersecretion of catecholamine in PHEO.
ET-1
produced in normal and tumor adrenal tissues may regulate aldosterone and catecholamine secretion from adrenals in a paracrine/autocrine fashion.
...
PMID:Immunoreactive endothelin-1 and its receptors in human adrenal tissues. 959 40