Magnesium (Mg2+) is one of the most abundant ions in the body. In the
human body, Mg2+ plays important roles including cofactors in many cru
cial enzyme systems, especially those involving energy transfer, stora
ge and utilization. Alteration of the concentration of Mg2+ may cause
neuromuscular hyperactivity, psychiatric disturbances, calcium/potassi
um abnormalities, and overactivity of cardiac muscle. Most information
on the effect of Mg2+ on muscle contraction has been obtained from st
udies on cardiac, skeletal, and vascular muscle; much less is known ab
out the effect of Mg2+ in other smooth muscle systems. In the current
study, we investigated the effect of Mg2+ on the contraction and intra
cellular free calcium of rabbit urinary bladder detrusor muscle in res
ponse to carbachol and transmural field stimulation (FS). The results
can be summarized as follows: (1) Reduction of the concentration of ma
gnesium [Mg2+] from normal Tyrode's solution enhanced the spontaneous
basal activity, whereas addition of Mg2+ gradually abolished this spon
taneous activity. (2) Muscle contraction induced by FS or carbachol wa
s enhanced in Mg2+-free Tyrode's solution. Addition of Mg2+ inhibited
the response to both forms of stimulation in a dose-dependent manner.
(3) Inhibitory effects of Mg2+ were potentiated when the Ca2+ concentr
ation in the Tyrode's solution was reduced to 0.6 mM, whereas increasi
ng the extracellular concentration of Ca2+ (5.4 mM) reduced the inhibi
tory effects of Mg2+. (4) Using FURA-2 to monitor intracellular free c
alcium simultaneous with contractile tension, we demonstrated that the
alterations in the contractile responses observed at different concen
trations of extracellular Mg2+ correlated with similar changes in intr
acellular free calcium. We conclude from this study that Mg2+ can sign
ificantly alter the contractile responses to FS and muscarinic stimula
tion by alteration of calcium influx during contraction.