saxitoxin and Heart-Diseases

saxitoxin has been researched along with Heart-Diseases* in 2 studies

Other Studies

2 other study(ies) available for saxitoxin and Heart-Diseases

ArticleYear
Morbidity and mortality in stranded Cook Inlet beluga whales Delphinapterus leucas.
    Diseases of aquatic organisms, 2015, May-11, Volume: 114, Issue:1

    The endangered Cook Inlet (Alaska, USA) stock of beluga whales Delphinapterus leucas declined 47% between 1994 and 1998, from an estimated 653 whales to 347 whales, with a continued decline to approximately 312 in 2012. Between 1998 and 2013, 164 known dead strandings were reported by the National Marine Fisheries Service. Only 38 of these animals, or 23% of the known stranded carcasses, were necropsied. Carcasses were found between April and October. The majority of animals necropsied were adults (n=25), followed by juveniles (n=6), calves (n=3), and aborted fetuses (n=4). Eight of the 11 mature females were pregnant, post-partum, or lactating. Many (82%) of these belugas were in moderate to advanced autolysis, which hampered determination of a cause of death (COD). Each animal had a single primary COD assigned within a broad set of categories. The CODs were unknown (29%), trauma (18%), perinatal mortality (13%), mass stranding (13%), single stranding (11%), malnutrition (8%), or disease (8%). Other disease processes were coded as contributory or incidental to COD. Multiple animals had mild to moderate verminous pneumonia due to Stenurus arctomarinus, renal granulomas due to Crassicauda giliakiana, and ulcerative gastritis due to Anisakis sp. Each stranding affords a unique opportunity to obtain natural history data and evidence of human interactions, and, by long-term monitoring, to characterize pathologies of importance to individual and population health.

    Topics: Alaska; Animals; Bacterial Infections; Beluga Whale; Female; Heart Diseases; Kainic Acid; Male; Malnutrition; Pregnancy; Saxitoxin; Virus Diseases; Water Pollutants; Wounds and Injuries

2015
Calcium-antagonist receptors in the atrial tissue of patients with hypertrophic cardiomyopathy.
    The New England journal of medicine, 1989, Mar-23, Volume: 320, Issue:12

    Hypertrophic cardiomyopathy is characterized by a nondilated, hypertrophied left ventricle in the absence of any overt cause. A possible role of adrenergic innervation or of cellular calcium regulation is suggested by the presence of hyperdynamic left ventricular function and by the clinical and symptomatic improvement seen in patients treated with beta-receptor antagonists or calcium antagonists. Therefore, we measured the density of calcium-antagonist receptors and beta-adrenoceptors in the atrial myocardium of 16 patients with hypertrophic cardiomyopathy and 19 patients with various other cardiac disorders. For comparison, we also measured the number of voltage-sensitive sodium channels. Calcium-antagonist binding sites, measured as the amount of dihydropyridine bound to atrial tissue, were increased by 33 percent in patients with hypertrophic cardiomyopathy (mean [+/- SD], 397 +/- 104 fmol per milligram of protein in patients with hypertrophic cardiomyopathy, as compared with 299 +/- 108 in patients with other cardiac disorders; P less than 0.01). The densities of saxitoxin-binding sites on voltage-sensitive sodium channels and beta-adrenoceptors were the same in the two groups, although the density of beta-adrenoceptors was higher in atrial samples from patients receiving beta-receptor antagonists (165 +/- 86 fmol per milligram of protein [patients receiving beta-blockers] vs. 85 +/- 60 [patients not receiving beta-blockers]; P less than 0.04). The increase in the number of calcium-antagonist receptors in hypertrophic cardiomyopathy suggests that abnormal calcium fluxes through voltage-sensitive calcium channels may play a pathophysiologic part in the disease.

    Topics: Adolescent; Adult; Aged; Calcium Channel Blockers; Calcium Channels; Cardiomyopathy, Hypertrophic; Child; Female; Heart Atria; Heart Diseases; Heart Septum; Hemodynamics; Humans; Iodocyanopindolol; Male; Middle Aged; Myocardium; Pindolol; Receptors, Adrenergic, beta; Receptors, Nicotinic; Saxitoxin

1989