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  • Electronic Resource  (7)
  • Scrophulariaceae  (3)
  • Cerebral ischemia  (2)
  • Osteoclast-like cell formation  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Phenolic glycosides from diseased roots of Rehmannia glutinosa var. purpurea
    Amsterdam : Elsevier
    Phytochemistry 26 (1987), S. 983-986 
    Details
    ISSN: 0031-9422
    Keywords: Rehmannia glutinosa ; Scrophulariaceae ; antimicrobial activity. ; caffeoyl glycoside of 3,4-dihydroxyphenethyl alcohol ; stress compound
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/S0031-9422(00)82331-6
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  • 2
    Electronic Resource
    Electronic Resource
    Phenolic glycoside composition of leaves and callus cultures of Digitalis purpurea
    Amsterdam : Elsevier
    Phytochemistry 26 (1987), S. 3225-3227 
    Details
    ISSN: 0031-9422
    Keywords: Digitalis purpurea ; Scrophulariaceae ; comparative study, callus culture ; phenolic glycoside.
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/S0031-9422(00)82474-7
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Constituents of regenerated and shoot cultured root tissue of Rehmannia glutinosa
    Amsterdam : Elsevier
    Phytochemistry 28 (1989), S. 2331-2332 
    Details
    ISSN: 0031-9422
    Keywords: Rehmannia glutinosa ; Scrophulariaceae ; caffeoyl glycosides. ; callus culture ; iridoid glycoside ; regeneration ; root culture
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/S0031-9422(00)97978-0
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Temporal profile of serum albumin extravasation following cerebral ischemia in a newly established reproducible gerbil model for vasogenic brain edema: a combined immunohistochemical and dye tracer analysis (1991)
    Springer
    Acta neuropathologica 82 (1991), S. 164-171 
    Details
    ISSN: 1432-0533
    Keywords: Gerbil ; Cerebral ischemia ; Vasogenic brain edema ; Immunohistochemistry ; Albumin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We investigated the temporal profile of the extravasation of serum albumin in a reproducible gerbil model of unilateral cerebral ischemia, using immunohistochemical and dye-tracer techniques to evaluate albumin accumulation and the occurrence of active extravasation, respectively. After 30 min of cerebral ischemia and subsequent reperfusion, immunostaining for albumin became visible in the lateral part of the thalamus during the first 3 h, and then expanded to other brain regions up to 24 h. At both 24 h and 3 days after reperfusion, massive extravasation of albumin was noted in the whole ischemic hemisphere, and this had decreased again by 7 days after reperfusion. The extent and the degree of albumin immunopositivity were almost the same in all animals examined at each period after reperfusion. The extravasation of Evans blue, which was allowed to circulate for 30 min before death, was limited to the lateral part of the thalamus during the first 6 h of reperfusion. In the circumscribed area of massive albumin extravasation, many neurons were immunopositive for albumin; most of these neurons appeared to be intact and also showed immunostaining for microtubule-associated protein 2. The current investigation clearly demonstrated that (1) albumin extravasation was produced with reliable reproducibility in this model, (2) the lateral part of the thalamus was the region most vulnerable to ischemic blood-brain barrier damage, and (3) many apparently intact neurons in the ischemic region were positive for albumin.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00294441
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  • 5
    Electronic Resource
    Electronic Resource
    The characteristics of blood-brain barrier in three different conditions — infarction, selective neuronal death and selective loss of presynaptic terminals — following cerebral ischemia (1992)
    Springer
    Acta neuropathologica 84 (1992), S. 378-386 
    Details
    ISSN: 1432-0533
    Keywords: Blood-brain barrier ; Cerebral ischemia ; Albumin ; Synapsin I ; Microtubule-associated protein 2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We investigated the extravasation of serum albumin using immunohistochemistry in three different conditions, i.e., infarction, selective neuronal death and selective loss of presynaptic terminals following cerebral ischemia in gerbils. In selective neuronal death, which is typically found in the CA1 neurons of the hippocampus after 5-min bilateral cerebral ischemia, selective damage of postsynaptic components with intact presynaptic sites was demonstrated by immunohistochemical examination for microtubule-associated protein 2 and synapsin I, and albumin extravasation did not become apparent before postsynaptic structures were destroyed. In cerebral infarction, which was consistently observed in the thalamus after 15-min forebrain ischemia, massive albumin extravasation was visible early after ischemia due probably to the ischemic endothelial necrosis. In selective loss of presynaptic terminals, which was detected at the molecular layer of the dentate gyrus in the contralateral, nonischemic hippocampus after unilateral cerebral ischemia, immunoreaction for albumin was not visualized. Since endothelium and glial cells were intact in morphological aspects in selective damage of both pre- and postsynaptic sites, it was thought that extravasation was facilitated by the stimulation of endothelial cells and glial cells with unknown factors that were induced by the destruction of post- but not presynaptic elements.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00227664
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  • 6
    Electronic Resource
    Electronic Resource
    Effects of lead on osteoclast-like cell formation in mouse bone marrow cell cultures (1994)
    Springer
    Calcified tissue international 54 (1994), S. 165-169 
    Details
    ISSN: 1432-0827
    Keywords: Lead ; Prostaglandin E2 ; Osteoclast-like cell formation ; Mouse bone marrow cells ; Cyclic adenosine 3′,5′-monophosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Abstract To examine an effect of lead (Pb) on the process of osteoclast-like cell formation from its progenitors, we used a mouse bone marrow culture system in which osteoclast-like multinucleated cells (MNCs) were formed in response to bone-resorbing agents. In a 9-day culture period, Pb dose-dependently stimulated MNC formation over the concentration range 2–10 μM, whereas at 40 μM Pb, MNC formation declined. In an 11-day culture period, MNC formation reached a maximum at 5 μM Pb and decreased with increasing concentration of Pb at 10–40 μM. Pb-stimulated MNC formation was inhibited by both indomethacin and SC19220, an antagonist of prostaglandin E2 (PGE2) receptor. Pb stimulated the production of PGE2 in marrow cell cultures, suggesting that Pb-stimulated MNC formation is dependent on the production of PGE2. 3-Isobutyl-1-methylxanthine potentiated Pb-stimulated MNC formation and 2′,5′-dideoxyadenosine, an inhibitor of adenylate cyclase, inhibited it. A calcium ionophore A23187 increased Pb-induced MNC formation and verapamil, a calcium channel blocker, depressed it. It is possible that a PGE2-induced increase in the levels of cyclic adenosine 3′,5′-monophosphate (cAMP) and calcium ions in marrow cells is involved in Pb-induced MNC formation. Pb and parathyroid hormone showed a synergistic stimulation on MNC formation. From these results, Pb is thought to induce osteoclast-like cell formation by a mechanism involving PGE2 which increases the intracellular levels of cAMP and calcium ions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00296069
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  • 7
    Electronic Resource
    Electronic Resource
    Calcium regulating activity of 26,27-dimethyl analog of 24R,25-dihydroxyvitamin D3 (1994)
    Springer
    Calcified tissue international 55 (1994), S. 190-197 
    Details
    ISSN: 1432-0827
    Keywords: Bone resorption ; Osteoclast-like cell formation ; Bone Ca mobilization ; Intestinal Ca transport ; 24R,25-dihydroxy-26,27-dimethylvitamin D3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Abstract To determine the possibility that methyl substitution in 26- and 27-positions of 24R,25-dihydroxyvitamin D3 [24,25(OH)2D3] alters activities of the original compound, the effects of 24,25(OH)2D3 on calcium (Ca) regulating activity were compared with those of its methyl analog [24,25(OH)2(CH3)2D3] in addition to 1α,25-dihydroxyvitamin D3 [1,25(OH)2D3]. 24,25(OH)2D3 at 10-6 M and 24,25(OH)2(CH3)2D3 at 10-7 M and above significantly stimulated both bone resorption in neonatal mouse calvaria cultures and formation of osteoclast-like multinucleated cells (MNC) in mouse bone marrow cultures. A stimulative effect of 1,25(OH)2D3 on bone resorption and MNC formation was recognized in very low concentrations (10-11 M and above). Although a potency of 24,25(OH)2(CH3)2D3 in stimulating bone calcium (Ca) mobilization and intestinal Ca transport was higher than that of 24,25(OH)2D3, the potencies of both compounds were similar to that of 1,25(OH)2D3 unlike in vitro experiments. As 1,24R,25-trihydroxy-26,27-dimethylvitamin D3 showed almost the same effect as 24,25(OH)2(CH3)2D3, the dihydroxy form is suggested to be hydroxylated at 1α position and converted to trihydroxy form in vitamin D-deficient rats. From these results, methyl substitution in 26- and 27-position of 24,25(OH)2D3 was found to elevate Ca regulating activity of the original compound. In addition, it is suggested that the basis for a similarity in potency between 1,25(OH)2D3 and 24,25(OH)2D3 or its dimethyl analog in vitamin D-deficient rats is likely the result of 1 α-hydroxylation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00425874
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