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Acta Physiologica Congress

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Acta Physiologica 2007; Volume 191, Supplement 658
Joint Meeting of The Slovak Physiological Society, The Physiological Society and The Federation of European Physiological Societies
9/11/2007-9/14/2007
Bratislava, Slovakia


MANGANESE SUPPLEMENTATION AFFECTS ENDOTHELIUM-DEPENDENT RELAXATION IN RATS
Abstract number: PF18-145

Serban1 2 D.N., Stoica3 B., Hogas1 M., Serban1 2 I.L., Budurca4 A.R., Nechifor5 ??

1Department of Physiology
2Center for the Study and Therapy of Pain
3Department of Biochemistry
4Clinic of Reparatory and Plastic Surgery
5Department of Pharmacology, University of Medicine and Pharmacy Grigore T. Popa, Iasi, Romania [email protected]

Aims: 

We have previously studied the effect of Mn (MnCl2 3 mg/kg, 7 days), in rats, healthy and with alloxan-induced diabetes and shown there is no correlation between Mn influences upon blood glucose and total antioxidant status. Then we found among others that endothelium-dependent relaxation (EDR) induced by carbachol (10-5 M) could be affected by Mn.

Methods: 

We have repeated the experiments in healthy rats using a higher Mn dose (MnCl2 10 mg/kg, 7 days). The animals were sacrificed to study the contractile activity in ring fragments from the aorta and small mesenteric arteries, in isometric conditions.

Results: 

We observed the reduction down to disappearance of EDR in both vessel types, with no changes in the contracting effects of K 40 mM and phenylephrine 10-5 M, or in the relaxing effects of nitroglycerine 10-6 M (upon both precontractions) and methoxy-verapamil (D600) 10-5 M (in K-contracted rings). In resistance arteries the EDHF component of EDR (in presence of 0.01 mM L-NAME and 0.01 mM indomethacin) was increased, partially compensating the reduction by Mn of nitric oxide dependent relaxation.

Conclusion: 

We show for the first time the appearance of toxic Mn effects upon endothelium at doses way bellow those recognized as toxic at the hepatic and neural level.

*CNCSIS grant A/1222 **CNCSIS grant interdisciplinary platform/68

To cite this abstract, please use the following information:
Acta Physiologica 2007; Volume 191, Supplement 658 :PF18-145

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