Processes for sodium permeability inactivation in the myelinated nerve fibre of the frog (Xenopus laevis).
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to T Brismar.
Explore the source record for details and available documents.
1. The nodal currents of single myelinated nerve fibres were recorded under potential clamp conditions, and the effect of [Ca], [Na] and [K] in the external solution on some of the Na permeability properties were analysed. 2. [Ca], [Na] and [K] all affected the position of the steady-state Na inactivation (h) curve on the potential axis. The curve was displaced in positive direction by high ionic concentration. 3. The shift associated to different [Ca] was largest in low [Na] and [K]. Similarly the shift associated to different [Na] and [K] was largest in low [Ca]. 4. The maximum peak sodium permeability (max. peak - PNa) was affected by the [Ca], [Na] and [K]. It was greater in (i) low [Ca], (ii) high ([Na] + [K]) and (iii) high [Na]:[K] ratio. 5. The effect of [Ca] on peak - Na was mainly a consequence of a change in PNa (which is the value of PNa if activation were complete, m = 1, and inactivation fully removed, h = 1).
Explore the source record for details and available documents.
Explore the source record for details and available documents.
We studied the occurrence of osteopenia, as reflected by decreased cortical bone thickness, in a nonobese animal model of hereditary non-insulin-dependent diabetes with long duration, i.e., 8-month-old Goto-Kakizaki (GK) rats. In addition, motor nerve-conduction velocity was measured in the GK rats. Age- and weight-matched Wistar rats served as controls. The GK rats displayed marked glucose intolerance, as compared to control rats, in an intraperitoneal glucose tolerance test. Decreased cortical bone thickness by approximately 15%, was evident in X-ray analysis of metatarsal bones (p < 0.001) and humerus (p < 0.05) of the GK rats. Motor nerve-conduction velocity, measured in the sciatic nerve, was also decreased (by 10%) in the GK as compared with the age-matched control rats (p < 0.05). In conclusion, reduction of cortical bone thickness is present in 8-month-old GK rats, which simultaneously demonstrate signs of peripheral neuropathy. Thus, the GK rat appears to be a model of NIDDM suitable for studies of diabetic bone disease in the absence of obesity.