ArticleThe Journal of physiology1991
Stimulation-induced potentiation of T-type Ca2+ channel currents in myocytes from guinea-pig coronary artery.
Article in The Journal of physiology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 27 citations in OpenAlex.
- Reduced RhoA activity mediates acute alcohol intoxication-induced inhibition of lymphatic myogenic constriction despite increased cytosolic [Ca(2+) ].Microcirculation (New York, N.Y. : 1994) · 2013Article
- Paradoxical potentiation of neuronal T-type Ca2+ current by ATP at resting membrane potential.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004Article
- Low-voltage-activated ("T-Type") calcium channels in review.Journal of bioenergetics and biomembranes · 2003Review
- Modulation and pharmacology of low voltage-activated ("T-Type") calcium channels.Journal of bioenergetics and biomembranes · 2003Review
- Cloning and expression of the human T-type channel Ca(v)3.3: insights into prepulse facilitation.Biophysical journal · 2002Article
- Voltage-dependent modulation of T-type calcium channels by protein tyrosine phosphorylation.The EMBO journal · 1997Article
- Voltage-gated calcium channel currents in human coronary myocytes. Regulation by cyclic GMP and nitric oxide.The Journal of clinical investigation · 1997Article
- Facilitation of T-type calcium current in bullfrog atrial cells: voltage-dependent relief of a G protein inhibitory tone.The Journal of physiology · 1996Article
- Voltage-dependent potentiation of low-voltage-activated Ca2+ channel currents in cultured rat bone marrow cells.The Journal of physiology · 1995Article
- Ultra-slow voltage-dependent inactivation of the calcium current in guinea-pig and ferret ventricular myocytes.Pflugers Archiv : European journal of physiology · 1994Article
- Splice-variant changes of the Ca(V)3.2 T-type calcium channel mediate voltage-dependent facilitation and associate with cardiac hypertrophy and development.Channels (Austin, Tex.)Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. Whole-cell Ca2+ channel currents were studied in myocytes isolated from guinea-pig circumflex coronary artery at 36 degrees C and with 10 mM-Ba2+ (or Ca2+) as charge carrier. With 180 ms clamp steps from the holding potential of -100 mV, currents at -30 mV were carried mostly through the T-type calcium channels while at positive potentials currents were mostly of the L-type. 2. The increase in frequency of pulsing from 0.1 to 2.5 Hz resulted in a reduction of peak inward current ('negative staircase') with the 180 ms pulses to + 10 mV, but in a 2-fold potentiation ('positive staircase') with pulses to -30 mV. T-type currents and their frequency-mediated potentiation did not change significantly when Ba2+ was substituted by Ca2+ or Sr2+. 3. Potentiation of T-type currents was further analysed with a paired-pulse protocol: at a basal frequency of 0.1 Hz, a pre-pulse (inducing current I1) was followed by a 200 ms repolarization to -100 mV and a test pulse (inducing current I2). The potentiation could only be recorded using test pulses depolarizing the membrane to potentials between -40 and -10 mV; at more positive test potentials it was masked by the depressant effect of pre-pulses on the L-type current. 4. Potentiation of I2 by 200 ms pre-pulses started at pre-pulse potentials more positive than -60 mV and saturated at -20 mV (I2 potentiated by a factor 2.4). Between -20 and +130 mV the potentiation was not dependent on the pre-pulse potential suggesting that the influx of Ba2+ or Ca2+ is not required for this effect. Potentiation of I2 by a 10 s pre-pulse followed the voltage dependence of the steady-state inactivation curve of the T-type Ca2+ channel; potentiation became visible at potentials more positive than -80 mV and saturated at about -50 mV. 5. When changing the interval between two identical 200 ms pulses, the T-type current was found to recover completely from inactivation within 40 ms at -100 mV; at intervals of 160-320 ms maximal potentiation of I2 occurred. 6. With pre-pulses shorter than 200 ms, potentiation became attenuated when inactivation became less complete. When the potential during the interval between the pulses was -80 instead of -100 mV, maximal potentiation was reduced (I2 potentiated by a factor of 1.3 instead of 2.2) and occurred later (1.28 s). 7. Potentiated T-type currents inactivated faster.(ABSTRACT TRUNCATED AT 400 WORDS)
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