Effect of contrast media on beta-endorphin secretion

1988 ◽  
Vol 29 (6) ◽  
pp. 741-743 ◽  
Author(s):  
P. P. Harnish ◽  
J. Zuniga ◽  
F. K. Northington ◽  
P. A. Melrose ◽  
S. A. Joseph ◽  
...  
1988 ◽  
Vol 29 (6) ◽  
pp. 741-743 ◽  
Author(s):  
P. P. Harnish ◽  
J. Zuniga ◽  
F. K. Northington ◽  
P. A. Melrose ◽  
S. A. Joseph ◽  
...  

The central nervous system may be highly susceptible to the toxic effects of contrast media (CM). Previous experiments demonstrated that vasopressin is released after the intravenous administration of CM. The present study examined the response of the opiocortin system to CM. Neurons of the rat basal hypothalamus, dispersed and attached to Cytodex-3 beads, were perfused with sodium diatrizoate, metrizamide or iohexol (3 mg iodine/ml). The effluent was collected, and the beta-endorphin (B-E) content was measured by a radioimmunoassay technique. Results, normalized to the internal positive control, were compared with release from normal saline (negative control) by analysis of variance. Diatrizoate and metrizamide caused significant release of B-E (p < 0.03). Iohexol did not stimulate release of B-E. These results suggest that diatrizoate and metrizamide, but not iohexol, can stimulate the release of hormones from hypothalamic neurons. The phenomenon may play a role in some reactions to intravascular CM administration since these neurons are not protected by a blood-brain barrier.


1984 ◽  
Vol 30 (2) ◽  
pp. 311-314 ◽  
Author(s):  
V S Fang ◽  
R G Fessler ◽  
J R Rachlin ◽  
F D Brown

Abstract An effect of metrizamide, a contrast medium, on results of beta-endorphin radioimmunoassay was examined. We found that 1, 5, and 10 microL of the medium added to 100 microL of standard containing 0 to 500 pg of beta-endorphin shifted the standard curve to the left in proportion to the metrizamide concentration. Three other contrast media showed a similar effect at low concentrations of beta-endorphin. This effect of contrast media artificially increased results in radioimmunoassay of beta-endorphin in cerebrospinal fluid, the mean overestimate being 121.9% (range, 0 to 435%). For plasma samples, this effect of contrast media resulted in an average 11.7% overestimate of beta-endorphin (range, -16% to 41%). These observations bring into question the validity of a previous suggestion that an increase in beta-endorphin in cerebrospinal fluid after intracerebral electrical stimulation is the mechanism for stimulation-produced analgesia.


1988 ◽  
Vol 29 (6) ◽  
pp. 741-743
Author(s):  
P. P. Harnish ◽  
J. Zuniga ◽  
F. K. Northington ◽  
P. A. Melrose ◽  
S. A. Joseph ◽  
...  

2010 ◽  
Author(s):  
Ilona S. Yim ◽  
Laura M. Glynn ◽  
Christine Dunkel Schetter ◽  
Calvin J. Hobel ◽  
Aleksandra Chicz-Demet ◽  
...  

1972 ◽  
Vol 11 (03) ◽  
pp. 265-269
Author(s):  
P. Strohal ◽  
D. Huljev ◽  
K. Filjak ◽  
D. Cvrtila ◽  
Š. Spaventi

La possibilité d’obtenir „Biligraphine“ marquée par 131I d’une activité hautement spécifique a été examinée en vue d’obtenir une préparation convenable pour le diagnostic scintigraphique du tract hépato-biliaire avec l’emploi d’un volume réduit du moyen de contraste.Les résultats ont montré que la meilleure contribution de la réaction est obtenue quand le matériel est traité pendant 11 heures à une température de 150—180° C. Après cette période environ 90% de 131I est entré dans le Biligraphine. Le reste de l’iodide radioactif libre s’élimine por un échangeur d’ions.Nous pouvons conclure que la méthode de l’échange homogène offre de bonnes possibilités pour le marquage des moyens de contraste et qu’elle est réalisable par un procédé relativement simple.


Contrast- induced nephropathy (CIN) is an elevation of serum creatinine of ≥ 0.5 mg/dL from baseline after two to three days of exposure to contrast substance if there is no other cause for acute kidney injury. Atorvastatin may protect normal kidney physiology from contrast- induced kidney injury by effects unrelated to hypolipidemia termed pleiotropic effect by decline of endothelin production, angiotensin system down regulation, and under expression of endothelial adhesion molecules. This study was conducted to assess the strategy by which atorvastatin can achieve protective effect for kidneys after exposure to contrast media in an animal model. A 40 male rats were distributed randomly into 4 groups; ten rats for each: group (1): given normal saline; group (2): CIN group given iopromide as contrast media; group (3): given atorvastatin (20mg/kg) and iopromide; and group (4): given atorvastatin (40mg/kg) and iopromide. Blood collected by cardiac puncture for detection of serum glutathione, malondialdehyde, matrix metalloproteinase-9, and interleukin-18. The results have shown a significant increase in inflammatory and oxidative stress markers in contrast media group, and significant reduction in these markers in atorvastatin treated groups, in a dose-dependent manner. As conclusion, atorvastatin mechanism for protection against CIN in a dose-dependent manner can mediate by anti-inflammatory and antioxidant effects.


2012 ◽  
Vol 5 (1) ◽  
pp. 37-43
Author(s):  
ABMM Alam ◽  
M Moniruzzaman ◽  
MB Alam ◽  
N Islam ◽  
F Khatoon ◽  
...  

Background: CIN has gained increased attention in the clinical setting, particularly during cardiac intervention but also in many other radiological procedures in which iodinated contrast media are used. There is at present good clinical evidence from well-controlled randomized studies that CIN is a common cause of acute renal dysfunction.Methodology: This was a prospective study conducted among the patients who underwent coronary angiography and percutaneous coronary intervention in the Department of Cardiology, Dhaka Medical College Hospital during January 2010 to December 2010. A total of 111 patients age range from 25 to 75 years were included in the study. Serum creatinine level at baseline and at the end of 48 hours was done in all these patients. Study population was divided into two groups according to development of acute kidney injury (AKI). Group-I = AKI, Group II = Not developed AKI. Results: AKI developed 11.7% of the study patient. DM and Preexisting renal insufficiency were significantly higher in group I patients. HTN was (61.5% Vs 44.9%) higher in group I but not significantly. History of ACE inhibitor/ARB, NSAID intake and LVEF <40% were significantly higher in group I patients. The mean±SD volume of CM (Contrast Media) were 156.9±44.8 ml and 115.4±30.0 ml in group I and group II respectively, which was significant. The mean±SD of serum creatinine after 48-72 hours of CAG/PCI was 1.4±0.37 mg/dl and 1.1±0.2 mg/dl in group I and group II respectively. The serum creatinine level increased significantly (p<0.05) after 48-72 hours of CAG/PCI in group I. In group II, S. creatinine level increased but not significant (p>0.05). Impaired renal function was found 76.9% and 2.0% in group I and group II respectively. DM, HTN, preexisting renal insufficiency, ACE inhibitor/ARB, NSAIDs, contrast volume (>150 ml), eGFR (<60 ml/min/ 1.73m2) and LVEF (<40%) are significantly (p0.05) associated for CIN development.Conclusion: CIN is an iatrogenic but preventable disorder results from the administration of contract media. Although rare in the general population, CIN occurs frequently in patients with underlying renal dysfunction and diabetes. In patients with pre angiographic normal renal function, the prevalence is low but in pre-existing renal impairment it may pose a serious threat. Thus risk factors are synergistic in their ability to predispose to the development of CIN. A careful risk-benefit analysis must always be performed prior to the administration of contrast media to patients at risk for CIN. DOI: http://dx.doi.org/10.3329/cardio.v5i1.12227 Cardiovasc. j. 2012; 5(1): 37-43


1987 ◽  
Vol 23 (4) ◽  
pp. 658
Author(s):  
J H Park ◽  
S H Kim ◽  
M J Shin ◽  
J C Kim ◽  
K W Minn ◽  
...  

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