Protein Information

ID 318
Name Potassium channel (protein family or complex)
Synonyms Potassium channel

Compound Information

ID 332
Name 4-aminopyridine
CAS 4-pyridinamine

Reference

PubMed Abstract RScore(About this table)
14594030 Fu ZJ, Cheng HW, Zhang LF, Ma J, Zhang LN, Ma XW: [Changes of potassium channel activity of hindlimb arterial smooth muscle cells in tail-suspended rats]. Space Med Med Eng. 2003 Aug;16(4):253-6.
OBJECTIVE: To examine the change of potassium channel function in hindlimb arterial smooth muscle cells in tail-suspended rats and to elucidate the underlying electro-physiological mechanisms responsible for the depressed vascular responsiveness of hindlimb arteries induced by simulated weightlessness. METHOD: The contractile responsiveness of femoral arterial rings of 1-wk and 4-wk tail-suspended rats to potassium channel blockers, tetraethylammonium chloride (TEA) and 4-aminopyridine (4-AP), were recorded, and the currents of large conductance calcium-dependent potassium channel (BK (Ca)) and voltage activated potassium channel (Kv) of vascular smooth muscle cells (VSMCs) in saphenous arteries from 1-wk tail-suspended rats were recorded using the whole cell recording mode of patch clamp technique. RESULT: The femoral arteries from of 1-wk and 4-wk tail-suspended rats showed a decreased contractile response to 60 mM KCl, and the ratio of their contractile responses induced by TEA or 4-AP to their responses induced by 60 mM KCl increased significantly after 1-wk and 4-wk simulated weightlessness. However no difference was found between 1-wk and 4-wk tail-suspended rats. The whole cell current recording showed that BK (Ca) current densities and K (v) current densities of VSMCs in saphenous artery increased significantly after 1-wk simulated weightlessness. CONCLUSION: The contractile response of hindlimb arteries to KCl decreased after simulated weightlessness. The activities of BK (Ca) and K (v) of smooth muscle cells in hindlimb arteries from tail-suspended rats increased, and these changes might be among the electro-physiological mechanisms involved in the depressed vasoreactivity of hindlimb arteries due to simulated weightlessness.
83(1,1,1,3)