Table 3.
NKA preparations | Experiment condition | Treatment | Effects on NKA | References |
---|---|---|---|---|
Microsomes or membranes from liver, kidney, heart, brain or pancreatic islets of rat, human and dog | Ca2+-free buffers | cAMP or PKA | ↓ATP hydrolysis | Limas et al. 1973; Tria et al. 1974; Braughler & Corder, 1978; Lingham & Sen 1982; Tugg et al. 1990 |
Membranes from rabbit kidney or ciliary processes | Ca2+-free buffer | cAMP or PKA | ↓ATP hydrolysis | Delamere et al. 1990 |
Rat renal tubule suspension | Ca2+-free buffer | Forskolin | ↓ATP hydrolysis | Hussian et al. 1997 |
Isolated rabbit iris–ciliary body | Ca2+-free buffer | cAMP | ↓Rb+ uptake | Delamere et al. 1990 |
Isolated rat renal tubules | Buffer 0.25 mM Ca2+ | cAMP | ↓ATP hydrolysis* | Fryckstedt & Aperia, 1992; Satoh et al. 1993; Holtbäck et al. 1998 |
Mouse fibroblast LTK− cells | [Ca2+]i not increased | cAMP | ↓ATP hudrolysis | Horiuchi et al. 1993 |
HeLa cells | [Ca2+]i~nM | cAMP | ↓Rb+ uptake* | Middleton et al. 1990 |
Isolated guinea-pig myocytes | [Ca2+]i<150 nM | PKA | ↓pump current | Gao et al. 1992 |
Isolated guinea-pig myocytes | [Ca2+]i>150 nM | PKA | ↑pump current | Gao et al. 1992 |
Isolated rabbit renal tubules | Buffer 1.8 nM Ca2+; low K+ (0.1 mM) pretreatment | cAMP or forskolin | ↑transmembrane potential | Breton et al. 1994 |
Isolated shark rectal gland cells | Buffer 2.5 mM Ca2+ | cAMP | ↑Rb+ uptake | Marver et al. 1986 |
Xenopus oocytes | Buffer Ca2+ 2mM; K+-free pretreatment and oocyte injection | cAMP | ↑pump current | Vasiloets et al. 1992 |
Purified NKA from rat kidney and shark rectal gland | Ca2+-free buffers | PKC | ↓ATP hydrolysis | Bertorello et al. 1991; Logvinenko et al. 1996 |
MDCK cells | Ca2+-free buffer | PMA/OAG | ↓ATP hydrolysis | Shahedi et al. 1992 |
Isolated rat renal tubules | Buffer 0.25 mM Ca2+ | PDBu | ↓ATP hydrolysis | Bertorello & Aperia, 1989; Satoh et al. 1993 |
Isolated rat choroid plexus | Buffer 0.25 mM Ca2+ | PDBu | ↓ATP hydrolysis | Fisone et al. 1995 |
Cultured rat tubule cells | Buffer 0.4 mM Ca2+ | PMA | ↓Rb+ uptake | Sinfh & Linas, 1997 |
A6 cells | Buffer 1.0 mM Ca2+ | PMA | ↑pump current | Beron et al. 1997 |
Isolated rat hepatocytes | [Ca2+]i∼250 nM | PMA | ↑Rb+ uptake | Lynch et al. 1986 |
Cultured skeletal muscle | Buffer 0.7 mM Ca2+; K+- free pretreatment | Phorbol esters | ↑Rb+ uptake | Sampson et al. 1994 |
Isolated rat renal tubules | Buffer 1.0 mM Ca2+; osmolarity 400mosmol kg−1; k+-free and low Rb+ pretreatment | PDBu | ↑or no change in Rb+ uptake/ATP hydrolysis | Feraille et al. 1995 |
Cultured human ciliary epithelium | Buffer 2.6 mM Ca2+ | PDBu | ↑Rb+ uptake | Mito & Delamere, 1993 |
Cultured rabbit non-pigmented ciliary epithelium | Buffer 2.5 mM Ca2+ | PDBu | ↑Rb+ uptake | Delamere et al. 1997 |
The decreased NKA activity was abolished in the presence of agents that increase [Ca2+]i PDBu, 4-phorbol 12,13-dibutyrate.