Effects of temperature on slow and fast inactivation of rat skeletal muscle Na+channels.
نویسنده
چکیده
Patch-clamp studies of mammalian skeletal muscle Na+ channels are commonly done at subphysiological temperatures, usually room temperature. However, at subphysiological temperatures, most Na+ channels are inactivated at the cell resting potential. This study examined the effects of temperature on fast and slow inactivation of Na+ channels to determine if temperature changed the fraction of Na+ channels that were excitable at resting potential. The loose patch voltage clamp recorded Na+ currents ( I Na) in vitro at 19, 25, 31, and 37°C from the sarcolemma of rat type IIb fast-twitch omohyoid skeletal muscle fibers. Temperature affected the fraction of Na+ channels that were excitable at the resting potential. At 19°C, only 30% of channels were excitable at the resting potential. In contrast, at 37°C, 93% of Na+ channels were excitable at the resting potential. Temperature did not alter the resting potential or the voltage dependencies of activation or fast inactivation. I Na available at the resting potential increased with temperature because the steady-state voltage dependence of slow inactivation shifted in a depolarizing direction with increasing temperature. The membrane potential at which half of the Na+channels were in the slow inactivated state was shifted by +16 mV at 37°C compared with 19°C. Consequently, the low availability of excitable Na+ channels at subphysiological temperatures resulted from channels being in the slow, inactivated state at the resting potential.
منابع مشابه
Effects of temperature on slow and fast inactivation of rat skeletal muscle Na1 channels
Ruff, Robert L. Effects of temperature on slow and fast inactivation of rat skeletal muscle Na1 channels. Am. J. Physiol. 277 (Cell Physiol. 46): C937–C947, 1999.—Patchclamp studies of mammalian skeletal muscle Na1 channels are commonly done at subphysiological temperatures, usually room temperature. However, at subphysiological temperatures, most Na1 channels are inactivated at the cell restin...
متن کاملFiber type conversion alters inactivation of voltage-dependent sodium currents in murine C2C12 skeletal muscle cells.
Each skeletal muscle of the body contains a unique composition of "fast" and "slow" muscle fibers, each of which is specialized for certain challenges. This composition is not static, and the muscle fibers are capable of adapting their molecular composition by altered gene expression (i.e., fiber type conversion). Whereas changes in the expression of contractile proteins and metabolic enzymes i...
متن کاملSlow Inactivation Does Not Affect Movement of the Fast Inactivation Gate in Voltage-gated Na+ Channels
Voltage-gated Na+ channels exhibit two forms of inactivation, one form (fast inactivation) takes effect on the order of milliseconds and the other (slow inactivation) on the order of seconds to minutes. While previous studies have suggested that fast and slow inactivation are structurally independent gating processes, little is known about the relationship between the two. In this study, we pro...
متن کاملEffects of lactate on the voltage-gated sodium channels of rat skeletal muscle: modulating current opinion.
During muscle contraction, lactate production and translocation across the membrane increase. While it has recently been shown that lactate anion acts on chloride channel, less is known regarding a potential effect on the voltage-gated sodium channel (Na(v)) of skeletal muscle. The electrophysiological properties of muscle Na(v) were studied in the absence and presence of lactate (10 mM) by usi...
متن کاملUltra-slow inactivation in mu1 Na+ channels is produced by a structural rearrangement of the outer vestibule.
While studying the adult rat skeletal muscle Na+ channel outer vestibule, we found that certain mutations of the lysine residue in the domain III P region at amino acid position 1237 of the alpha subunit, which is essential for the Na+ selectivity of the channel, produced substantial changes in the inactivation process. When skeletal muscle alpha subunits (micro1) with K1237 mutated to either s...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- American journal of physiology. Cell physiology
دوره 277 5 شماره
صفحات -
تاریخ انتشار 1999