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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 10 (1977), S. 167-182 
    ISSN: 1432-1432
    Keywords: Molecular evolution ; Phylogenetics ; Numerical taxonomy ; Snake venom toxins ; Elapidae ; Hydrophiidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Phylogenetic trees were constructed for 62 venom toxins of snakes ofProteroglyphae suborder using matrix method. The resulting tree fromMinimum Spanning Tree-Cluster Analysis technique had the lowest “percent deviation” (8.55). The taxonomic relationship of these toxins agrees very well with zoological opinions. However, the appearance of the tree did not directly provide a plausible evolutionary model for the toxins. A model was derived from nodal ancestral sequence calculations, comparisons between intra-and inter-generical rates of amino acid change, and generally held ideas about protein evolution. According to the model, short neurotoxin is the ancient form of snake venom toxins. The courses of evolution leading to the present intraspecific homologous toxins are explained by gene duplication and allelomorphism.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of biomedical science 3 (1996), S. 203-210 
    ISSN: 1423-0127
    Keywords: Ile7-angiotensin III ; Bestatin ; Osmotic minipump ; Drinking response ; Spontaneously hypertensive rats ; Normotensive rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We examined the physiologic role of endogenous brain angiotensin III (AIII), an active degradative product of angiotensin II, in drinking behavior. Adult, male spontaneously hypertensive (SH) and Wistar-Kyoto normotensive (WKY) rats that were instrumented with an intracerebroventricular (i.c.v.) cannula connected to an osmotic minipump for chronic infusion were used. 7-day i.c.v. infusion of the specific AIII antagonist, Ile7-AIII (10 or 100 pmol/min), resulted in no significant alteration in daily (24 h), diurnal (8:00 a.m.-8:00 p.m.) or nocturnal (8:00 p.m.-8:00 a.m.) basal water intake in both SH and WKY rats. Similar results were obtained with i.c.v. infusion of the aminopeptidase inhibitor, bestatin (150 or 300 pmol/min), given alone or simultaneously with Ile7-AIII (10 pmol/min). Rats that were water-deprived for the first 3 days of 7-day infusion of Ile7-AIII consumed significantly less water during the first 2 h after water became available. Furthermore, the accumulated water intake during the first 24 h was appreciably greater in SH than WKY rats. We interpret these results to suggest that the endogenous brain AIII may not be tonically involved in fluid homeostasis. Instead, it must be activated under conditions of dehydration, such as water deprivation, particularly in the SHRs, to initiate drinking behavior.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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