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  • 2000-2004  (2)
  • 1995-1999  (1)
  • 1
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The nuclear receptor heterodimers of liver X receptors (LXRs) are recently identified as key transcriptional regulators of genes involved in lipid homeostasis and inflammation. LXRs and their ligands are negative regulators of macrophage inflammatory gene expression. Multiple sclerosis (MS), a demyelinating disease of the central nervous system of unknown cause, is characterized by recurrent inflammation involving macrophages and their inflammatory mediators. Sweden belongs to the countries with a high MS incidence. In Italy, incidence is lower, with an exception for Sardinia where the incidence is even higher than that in Sweden. Subjects from Sardinia are ethnically more homogeneous and differ from Swedes, also regarding genetic background and environment. We studied LXRs and their related molecules of blood mononuclear cells (MNCs) from female patients with untreated relapsing-remitting MS from Sassari, Sardinia and Stockholm, Sweden. Sex- and age-matched healthy controls (HCs) were from both areas. mRNA expression was evaluated by real-time PCR. LXR-α was lower (P 〈 0.05) in MS (mean ± SEM: 3.1 ± 0.2; n = 37) compared to HC (3.6 ± 0.1; n = 37). LXR-α was lower in MS from Stockholm (2.6 ± 0.2; n = 22) compared to corresponding HC (3.4 ± 0.1; n = 22; P 〈 0.01) and compared to MS (3.8 ± 0.2; n = 15; P 〈 0.001) and HC (4 ± 0.2; n = 15; P 〈 0.001) from Sardinia. MS patients from Stockholm, but not from Sassari, also expressed lower (P 〈 0.05) LXR-β (−4.1 ± 0.4) compared to corresponding HC (−2.9 ± 0.3). MS from Stockholm was associated with higher ABCA-1 (6.1 ± 0.4 versus 5.0 ± 0.3; P 〈 0.05) and higher estrogen receptor-β-Cx (2.4 ± 0.4 versus 0.8 ± 0.4; P 〈 0.01) compared to corresponding HC. The HC from Sassari had higher androgen receptor (2.9 ± 0.2) compared to MS from Sassari (1.4 ± 0.3; P 〈 0.01), MS (1.3 ± 0.4; P 〈 0.01) and HC from Stockholm (1.2 ± 0.3; P 〈 0.01). MS from Sassari had lower cyclooxygenase-1 compared to corresponding HC (5.1 ± 0.4 versus 6.6 ± 0.3; P 〈 0.01) and lower prostaglandin-E (−0.03 ± 0.5) compared to the HC (1.4 ± 0.5; P 〈 0.05) and MS (2.7 ± 0.4; P 〈 0.05) and HC from Stockholm (1.9 ± 0.4, P 〈 0.001). Our findings identify LXRs and their related molecules as being involved in MS from Stockholm but not from Sassari, while sex hormone receptors seem to be involved in MS in Sassari.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In order to study estrogen effects on developing human neurons, we have established primary cultures of neurons and glia from 8–13-week human embryo cortex and spinal cord. The neuronal identity of the cultures was verified using the neuronal synaptic vesicle and neuronal endosomal membrane markers synaptotagmin, synapsin and synaptophysin, and the glial contribution to the mixed glial–neuronal cultures was verified using the glial marker glial fibrillary acidic protein (GFAP). We here report expression of estrogen receptor beta (ERβ) in these cells using RT-PCR and sequencing, RNAse protection assay, immunohistochemistry and immunoblotting. We found that both neuronal and mixed glial–neuronal cultures expressed ERβ. Treatment with 17β-estradiol gave an increased expression of ERβ in both types of cultures. These results suggest that ERβ is expressed in fetal brain and thus may mediate effects of estrogen in the developing nervous system. Furthermore, the results suggest that expression of ERβ in fetal brain may be regulated by estrogen.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0428
    Keywords: Keywords Glucose-6-phosphatase ; insulin release ; glucose metabolism ; glucocorticoid sensitivity ; transgenic mice.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Glucose-6-phosphatase (G6Pase) activity and the rate of glucose cycling are increased in islets from animal models of Type II (non-insulin-dependent) diabetes mellitus. Glucocorticoid treatment further stimulates these processes and inhibits glucose-induced insulin release. To determine whether these effects result from a direct action of glucocorticoids on the beta-cells, we used isolated islets. The islets were from transgenic mice overexpressing the glucocorticoid receptor in their beta-cells to increase the cells' sensitivity to glucocorticoid. Islets from transgenic and non-transgenic control mice utilized and oxidized the same amount of glucose. In contrast, islet G6Pase activity was 70 % higher, glucose cycling was increased threefold and insulin release was 30 % lower in islets from transgenic mice. Hepatic G6Pase activity was the same in transgenic and control mice. Dexamethasone administration increased G6Pase activity and glucose cycling and decreased insulin release in both transgenic and control mouse islets. We conclude that glucocorticoids stimulate islet G6Pase activity and glucose cycling by acting directly on the beta-cell. That activity may be linked to the inhibition of insulin release. [Diabetologia (1998) 41: 634–639]
    Type of Medium: Electronic Resource
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