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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 145 (1995), S. 217-232 
    ISSN: 1432-1424
    Keywords: Whole-cell recording ; Anion selectivity ; Cl-channel blockers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract During whole-cell patch-clamp recording from normal (nontransformed) human T lymphocytes a chloride current spontaneously activated in 〉98% of cells (n 〉 200) in the absence of applied osmotic or pressure gradients. However, some volume sensitivity was observed, as negative pressure pulses reduced the current. With iso-osmotic bath and pipette solutions the peak amplitude built up (time constant ≈23 sec at room temperature), a variable-duration plateau phase followed, then the current ran down spontaneously (time constant ≈280 sec). The anion permeability sequence, calculated from reversal potentials was I−, Br− 〉 NO 3 − , Cl− 〉 CH3SO 3 − , HCO 3 − 〉 CH3COO− 〉 F− 〉 aspartate, gluconate, SO 4 2− and there was no measurable monovalent cation permeability. The Cl− current was independent of time during long voltage steps and there was no evidence of voltage-dependent gating; however, the current showed intrinsic outward rectification in symmetrical Cl− solutions. The conductance of the channels underlying the whole-cell current was calculated from fluctuation analysis, using power-spectral density and variance-vs.-mean analysis. Both methods yielded a single channel conductance of about 0.6 pS at −70 mV (close to the normal resting potential of T lymphocytes). The power spectral density function was best fit by the sum of two Lorentzian functions, with corner frequencies of 30 and 295 Hz, corresponding to mean open times of 0.54 and 5.13 msec. The pharmacological profile included rapid block by external application of flufenamic acid (50 μm), 5-nitro-2-(3-phenylpropylamino)-benzoic acid (NPPB, 100 μm, [6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-y1) oxy] acetic acid (IAA-94, 250 μm) or 100 μm 1,9-dideoxyforskolin. The stilbene derivatives DIDS (4,4′-diisothiocyano-2,2′ di-sulphonic acid stilbene, 500 μm) and SITS (4-acetamido-4′-isothiocyano-2, 2′-disulphonic acid stilbene, 500 μm) prevented buildup of Cl− current after a 30-min preincubation at 500 μm. When tested in a mitogenic assay, DIDS, flufenamic acid, NPPB and IAA-94 all inhibited T-cell proliferation, suggesting a physiological function in addition to the observed volume sensitivity.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: The pathophysiology of traumatic spinal cord injury (SCI)involves abnormal activation of the neutral cysteine protease calpain I (EC3.4.22.17). In the present study we examined the effect of the calpaininhibitor CEP-4143 on cytoskeletal protection and neurological recovery afterSCI in adult rats. Microinjection of 50 mM CEP-4143 into the T7vertebral segment 10 min before a 35-g clip compression injury resulted ininhibition of calpain activation at 2 and 4 h postinjury, as determined bywestern blotting for calpain I-mediated spectrin degradation, andsignificantly attenuated the degradation of dephosphorylated NF200neurofilament protein at 4 and 8 h postinjury. To examine the in vivo chronicneuroprotective effects of CEP-4143, animals underwent microinjection withsaline or 50 mM CEP-4143 10 min before injury, followed by weeklyblinded behavioral assessments for 6 weeks. Animals receiving CEP-4143treatment showed significant improvement over saline-treated controls on theBasso Beattie Bresnahan locomotor rating scale (p 〈 0.02) andinclined plane test (p 〈 0.05). Counts of neurons in the red nucleus retrogradely labeled by fluorogold after introduction distal to the injury site were significantly higher in CEP-4143-treated animals. Finally, morphometric assessment of the injury site by computer-assisted image analysis revealed significant tissue preservation in CEP-4143-treated animals. We conclude that the calpain antagonist CEP-4143 exhibits biochemical, behavioral, and anatomical neuroprotection following traumatic SCI.
    Type of Medium: Electronic Resource
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