Relationship between nitric oxide (NO) and tumor necrosis factor (TNF-α) in cerebral control of thirst

Neuropeptides ◽  
1992 ◽  
Vol 22 (1) ◽  
pp. 12
Author(s):  
G. Calapai ◽  
F. Squadrito ◽  
M. Cilia ◽  
M.C. Marciano ◽  
G. Mazzaglia ◽  
...  
2013 ◽  
Vol 8 (9) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Kanidta Kaewkroek ◽  
Chatchai Wattanapiromsakul ◽  
Palangpon Kongsaeree ◽  
Supinya Tewtrakul

The ethanol extract of the rhizomes of Kaempferia marginata showed a potent inhibitory effect against lipopolysaccharide (LPS)-induced nitric oxide (NO) and tumor necrosis factor-alpha (TNF-α) release in RAW264.7 cells. Moreover, the partition with various organic solvents also inhibited NO production. One new pimarane-type diterpene, 1α-acetoxysandaracopimaradien-2α-ol (5), along with four known diterpenes (1–4), were isolated from the n-hexane and chloroform layers, respectively. Among these metabolites, compounds 1 and 4 were isolated for the first time from K. marginata. Compounds 1–5 showed significant inhibitory effects on NO production, with IC50 values ranging from 38.6 to 51.9 μM. Furthermore, compound 2 also exhibited significant activity against TNF-α release (IC50 = 48.3 μM). These findings may support the use of K. marginata by traditional doctors for treatment of inflammatory-related diseases.


2001 ◽  
Vol 226 (4) ◽  
pp. 296-300 ◽  
Author(s):  
Claudio A. Mastronardi ◽  
Wen H. Yu ◽  
Samuel M. McCann

Bacterial lipopolysaccharide (LPS) stimulates massive release of tumor necrosis factor-alpha (TNF-α) together with nitric oxide (NO) and a lessor release of leptin. We hypothesized that other types of stress such as that of surgery might also release these cytokines and NO. Adult male rats were anesthetized with ketamine/acepromazine/xylazine anesthesia (90 + 2 + 6 mg/ml, respectively) and an external jugular catheter was inserted for removal of blood samples (0.6 ml) at various times postoperatively. Plasma TNF-α was almost undetectable in decapitated rats and was near zero immediately following the placement of the jugular catheter (time zero [to]). As the rats awakened from anesthesia, there was a rise in TNF-α at 30 min that peaked at 2 hr with a 400-fold increase and then precipitously declined 40-fold to a level still greater than zero at 3 hr. At 6 hr on the following morning, TNF-α values were near zero, but following connection of tubing and withdrawal of the initial blood sample, there was a 100-fold increase 1 hr later, followed by a decline over the next 3 hr. In contrast, plasma [NO3/NO2] from decapitated rats was 117 μM. Values at t0 were decreased and plummeted 4-fold within 30 min, then rose slightly in the ensuing 3 hr. At 6 hr on the next day [NO3/NO2] values were lower than at t0 and declined gradually during the next 4 hr. Leptin gradually declined from pre-operative concentrations, reaching a minimum at 3 hr and its concentration was unaffected by the bleeding stress of the second day. We conclude that release of TNF-α, [NO3/NO2], and leptin are neurally controlled since plasma levels of all three declined as a result of anesthesia. TNF-α secretion was remarkably stress responsive, whereas NO release appeared to be suppressed by the combined operative and bleeding stress, and leptin was stress unresponsive.


Metabolism ◽  
2004 ◽  
Vol 53 (10) ◽  
pp. 1268-1273 ◽  
Author(s):  
Magdalena Olszanecka-Glinianowicz ◽  
Barbara Zahorska-Markiewicz ◽  
Joanna Janowska ◽  
Aleksander Zurakowski

Blood ◽  
1997 ◽  
Vol 90 (3) ◽  
pp. 1160-1167 ◽  
Author(s):  
Liang Yan ◽  
Shuibang Wang ◽  
Steven P. Rafferty ◽  
Robert A. Wesley ◽  
Robert L. Danner

Abstract Various functions of human phagocytes are modulated by nitric oxide (NO). We transfected the human U937 monoblastoid cell line with an expression vector containing human endothelial NO synthase (eNOS) or murine inducible NOS (iNOS) cDNA to study the regulatory role of NO without the nonspecific effects associated with exogenous NO sources. Western blot confirmed expression of eNOS or iNOS in respectively transfected cells, but not in naive or empty-vector transfected cells. Transfectants expressing iNOS, a calcium-independent enzyme, but not eNOS, a calcium-dependent enzyme, spontaneously produced NO (P < .001). The NO release from iNOS-transfected cells, as measured by nitrite and nitrate accumulation and by cyclic guanosine monophosphate (cGMP) increases in rat reporter cells, was inhibitable (P < .01 for both) with Nω-methyl-L-arginine (L-NMA), a NOS inhibitor. The eNOS transfectants were shown to contain functional enzyme by the conversion of L-arginine to L-citrulline in fractionated cells (P = .0001) and by exposing intact cells to calcium ionophore using the cGMP reporter cell assay (P = .0001). After differentiation with phorbol-12-myristate-13-acetate (PMA), iNOS transfectants produced more tumor necrosis factor-α (TNF-α) (124.9 ± 25.4 pg/5 × 105 cells per 24 hours) than did empty-vector transfected cells (21.9 ± 1.9 pg/5 × 105 cells per 24 hours; P = .02). This effect was inhibited by 500 μmol/L L-NMA (54.4 ± 3.1 pg/5 × 105 cells per 24 hours; P = .05). However, in the presence of high concentrations of lipopolysaccharide (1 μg/mL), which further increased NO production in iNOS transfected cells (P = .044), TNF-α production was similar comparing PMA-differentiated iNOS and empty-vector transfectants (12.2 ± 0.8 and 13.1 ± 1.7 ng/5 × 105 cells per 24 hours, respectively; P = .5). The results show that under certain conditions endogenously produced NO can upregulate TNF-α production in human phagocytes.


2008 ◽  
Vol 62 (4) ◽  
pp. 1330-1336 ◽  
Author(s):  
M. Angeles Muñoz-Fernández ◽  
Eva Cano ◽  
Catherine A. O'Donnell ◽  
Jackie Doyle ◽  
F. Y. Liew ◽  
...  

1992 ◽  
Vol 26 ◽  
pp. 166-167
Author(s):  
Gioacchino Calapai ◽  
Domenica Altavilla ◽  
Maria C. Marciano ◽  
Giampiero Mazzaglia ◽  
Marcello Cilia ◽  
...  

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