Author/Editor     Bunc, Matjaž; Strupi-Šuput, Jerneja; Vodovnik, Aleksander; Šuput, Dušan
Title     Toxic effects of head-to-tail 3-alkylpyridinium polymers isolated from the marine sponge Reniera sarai in rat
Type     članek
Source     Toxicon
Vol. and No.     Letnik 40, št. 7
Publication year     2002
Volume     str. 843-49
Language     eng
Abstract     Toxic water soluble polymeric 3-alkylpyridinium salts (poly APS; MW 18900 and 5520 Da) were isolated from the marine sponge Raniera sarai. In vitro they strongly inhibited acetylcholinesterase. In order to evaluate the role of acetylcholinesterase inhibition in toxin lethality, and to assess other possible lethal effects, in vivo experiments were performed on male Wistar rats, and ECG, blood pressure and breathing pattern were monitored. The results showed that none of khe animals died due to the acetylcholinesterase inhibitory action of poly-APS. Doses lower than 1 mg/kg caused only transient bradycardia and transient prolongation of expirium. At doses above 2.7 mg/kg of poly-APS all treated animals died, but signs were not typical of acetylcholinesterase inhibition. Arterial blood pressure fell to mid-circulatory pressure, and breathing stopped after a few breaths with an increase of the residual volume. Autopsy of the experimental animals that died due to the effects of the toxin revealed that mid-size and small sized blood vessels in the heart and lungs were filled with granular brownish material with inclusions of red blood cells and platelets. Data obtained on blood samples fmm animals treated with poly-APS also revealed numerous thrombocyte aggregates. In vitro poly-APS induced thrombocyte aggregation in a dose dependent manner. The acetylcholinesterase-inhibitory effects were most pronounced only at lower doses of poly-APS. With higher doses those effects were masked or covered by other, more pronounced and faster developing lethal effects of the toxin such as platelet aggregation. Therefore it is reasonable to assume that acetylcholinesterase inhibitory effects are not responsible for the lethal activity of the toxin.
Descriptors     PYRIDINIUM COMPOUNDS
ALKENES
ACETYLCHOLINESTERASE
PLATELET AGGREGATION
RATS, WISTAR
PORIFERA
ELECTROCARDIOGRAPHY
BLOOD PRESSURE
DOSE-RESPONSE RELATIONSHIP, DRUG