Lethal and haemorrhagic activity of Russell's Viper venom--neutralization by polyvalent, monovalent and toxoid antiserum

Lethal and haemorrhagic activity of Russell's Viper venom was compared against polyvalent bivalent commercial antiserum and monovalent antiserum raised in rabbit. Formaldehyde-detoxified venom offered 7-fold protection against lethal activity and 12.5-fold against haemorrhagic activity of the venom. Whole venom and formaldehyde-detoxified venom along with Freund's complete adjuvant, injected in rabbits produced high titre antiserum. Amongst all the six antiserum tested, the monovalent antiserum raised in rabbit, showed maximum precipitating bands in immunogeldiffusion and immunoelectrophoresis. The toxoid-antiserum offered maximum protection against the venom-induced lethality and the monovalent antiserum offered maximum protection against haemorrhagic activity.     

Repair of hair cells following mild trauma may involve extracellular chaperones

Sea anemones were subjected to mild trauma consisting of a 2 min immersion in calcium-depleted seawater. The trauma caused a loss of vibration sensitivity that spontaneously recovered within 50 min of returning the anemones to calcium containing seawater. Apparently, recovery is conferred by proteins contained in fraction gamma, a chromatographic fraction of homogenized mucus collected at the base of anemones allowed to recover from similar trauma. On silver stained SDS-PAGE gels, fraction gamma consists of a single band having an estimated mass of 55 kDa. Fraction gamma is alone sufficient to repair hair bundle mechanoreceptors in anemones. Its biological activity is enhanced in the presence of exogenously supplied ATP, but not GTP nor ADP-ribose. Biotinylated fraction gamma binds to hair bundles. The hypothesis that fraction gamma consists of Hsp60 proteins was tested. Commercial antibodies to Hsp60 label a band at 55 kDa in western blots. Hsp60 antibodies label hair bundles in traumatized anemones but not in untreated controls. Dilute Hsp60 antiserum (but not nonimmune serum) delays the spontaneous recovery of vibration sensitivity in anemones subjected to mild trauma. Thus, fraction gamma likely consists of Hsp60, or a Hsp60-like protein, that functions on the extracellular face of the plasma membrane to restore function to traumatized hair bundles.     

Effects of cytokinins and injury on the formation of shoot buds by leaves of Dendrophthoe falcata

Summary A number of cytokinins induce shoot buds on leaves obtained from embryonal tissue (diploid) or endosperm tissue (triploid) of Dendrophthoe falcata cultured in vitro. The buds develop either by division of an epidermal cell which finally is organized into a shoot meristem; or the epidermal cell first produces a callus which subsequently gives rise to shoot buds. Buds do not develop in the absence of cytokinins. Injury to the leaf plays a major role in the distribution and number of shoot buds formed. Normal leaves on the plant do not regenerate buds even in the presence of a cytokinin.     

Functional morphology of the caudal region of certain clupeiform and perciform fishes with reference to the taxonomy

The caudal anatomy (caudal skeleton, musculature, vascularization, innervation, and urohypophysis) and swimming behavior of three clupeiform and three perciform fishes: Elops hawaiensis (Cupeiformes: Elopidae), Oncorhynchus nerka (Cupeiformes: Salmonidae), Chanos chanos (Clupeiformes: Chanidae), Kuhlia sandvicensis (Perciformes: Kuhlidae), Apogon menesemus (Perciformes: Apogonidae), and Gnathanodon speciousus (Perciformes: Carangidae), were studdied. The taxonomic significance of caudal structures was determined and evaluated by detailed examination of differences in caudal anatomy. An interpretation of functional significance of these differences was attempted by relating them to observed differences in swimming behavior. The swimming behavior was studied by the observation of swimming activities of fish while resting or cruising and while feeding in the aquarium, and by an analysis of each frame of an 8 mm movie film of swimming activities. There are certain consistent and basic differences between all three species of the order Clupeiformes and all three species of the order Perciformes in respect to caudal structures. Although certain caudal structures show overlapping in number and/or complexity of arrangement, they seem to indicate more complex structural organization in Clupeiformes than Perciformes. The differences confirm the conclusion of others that the order Clupeiformes is more “primitive” than the order Perciformes. With respect to caudal structures of the three clupeiform species studied, E. hawaiensis is the most “primitive” and, of the three perciform species studied, K. sandvicensis is the most “primitive.” Caudal structural variations from one species to another are related to the mode of adaptation to swimming as well as to the evolutionary status of the species.     

Observation of carbonyl oxygen-π interaction in a metal complex

X-ray crystallography shows that [Ag₂L₂(H₂O)₂](BF₄)₂ where L is a 1:1 condensate of 1,2-diphenylethane-1,2-dione and 2-(2-aminoethyl pyridine), contains an Ag(I)-Ag(I) bond of length 2.979(2) Å and an angular, intraligand interaction of the keto O with the π cloud of the pyridine moiety (O-pyridine centroid = 3.12 Å). Model MP2/6-311++G(d,p) calculations indicate that the observed lone pair-π type interaction is stabilising and not merely a tolerated short contact.     

The blood-brain barrier and cerebral angiogenesis: lessons from the cold-injury model.

Brain injury is associated with an initial blood-brain barrier (BBB) breakdown, which can be life threatening. A second phase of BBB breakdown accompanies the angiogenesis occurring at the lesion margins. Studies of the molecular mechanisms involved in these processes are essential to determine targets for therapeutic intervention, as well as the time periods during which therapeutic intervention could ameliorate brain damage and thus improve the clinical outcome.     

Organ culture of adult amphibian heart: a fine structural analysis.

Pieces of hearts from adult newts were cultured up to 2 months. Within 7 days of culture, approximately 37% of the cardiac explants were attached to the substrate and more than 33% of the attached explants and approximately 15% of the unattached explants established pulsation rates ranging from 3 to 67 beats/min. The control and cultured explants were processed at weekly intervals for electron microscopy. The diameter of the control cardiac muscle cells ranged approximately 3-5 micron. The cell surface was provided with microvilli. The intercellular spaces ranged approximately 150-500 A. The intercalated discs lacked the step-like courses observed in the mammalian cardiac muscle. Sarcoplasmic reticulum was scanty. Desmosomal-dense materials were frequently continuous with the Z-bands of both control and cultured cardiac muscle cells. The transverse tubular system and gap junction were absent in newt ventricles. The functional implications of these characterisitics are discussed. At the end of 1 week of culture, the surfaces of the explants were covered by one or more layers of non-muscle cells, and the core of the explants consisted mostly of cardiac muscle cells. In a few cardiac muscle cells the myofibrillar organization was disrupted, resulting in the distribution of scattered patches of myofibrils and free myofilaments in the sarcoplasm. A small number of intact muscle cells contained a considerable number of dense granules in the sarcoplasm. At 15 days in culture, a large number of muscle cells showed structural features reminiscent of embryonic cardiac muscle cells. These cells possessed patches of myofibrils, scattered myofilaments and scanty sarcoplasmic reticulum along with other cellular organelles and inclusions. Several of these altered cardiac muscle cells contained mitotic figures. The cardiac explants maintained the initial beating rate until the end of 2 months of culture, except for the 11% of the explants which stopped beating. By 3-4 weeks in culture, most of the cardiac muscle cells possessed the altered cell morphology mentioned above. The explants after 60 days in culture became more flattened than the earlier explants. The intact cardiac muscle cells were rare, and the cores of the explants were mostly occupied by the altered cardiac muscle cells. It is evident from our studies that the cardiac muscle cells have undergone dedifferentiation in long-term culture, and that this dedifferentiation process has yet had no effect in the maintenance of contractility of the explants. Furthermore, these dedifferentiated cardiac muscle cells are capable of DNA synthesis and mitosis.     

Glucocorticoid effects on growth, and androgen receptor concentrations in DDT1MF-2 cell lines

The DDT1MF-2 smooth muscle tumor cell line contains receptors for and is differentially sensitive to androgens and glucocorticoids. Androgens stimulate and glucocorticoids inhibit growth. We now confirm that the latter involves the induction of a block in the G1 phase of the cell cycle. We have developed and characterized in vitro and in vivo a glucocorticoid resistant variant of this cell line, the DDT1MF-2-GR. Glucocorticoids specifically inhibit androgen induced androgen receptor augmentation in DDT1MF-2 cells, but not in the GR variant suggesting that growth inhibition is related to inhibition of androgen receptor augmentation. However, under optimal conditions for cell proliferation, when glucocorticoid inhibited growth is relieved by the exogenous addition of platelet derived growth factor, androgen receptor augmentation is still suppressed. Thus, androgen induced elevation in androgen receptor concentrations is not a prerequisite for cell proliferation. These results imply that in androgen responsive cells, although androgen stimulation of growth can be blocked by antagonism of androgen receptor mediated events, the antagonism can be bypassed by supplying the cells with exogenous growth factors. These results provoke speculation on how cells, which are dependent upon androgens for growth, become autonomous.