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. 2010 Mar 26;298(6):H1797–H1806. doi: 10.1152/ajpheart.00112.2010

Fig. 7.

Fig. 7.

Proposed signal transduction pathways for specific α1-AR subtype-mediated Ca2+-dependent and Ca2+-independent smooth muscle cell (SMC) contraction in adult and fetal CA. Left: α1A-AR and α1B-AR subtypes mediate production of Ins(1,4,5)P3, with the result of increasing intracellular Ca2+ release, and effect contraction in the Ca2+-dependent pathway in both fetus and adult. In addition, α1D-AR with dashed line indicates activation of Ins(1,4,5)P3 pathway only in adult. Right: fetus, in contrast to adult, α1B- and α1D-AR activate PKC, which in turn activates the extracellular regulated kinases ERK1/2 to stimulate gene expression to result in SMC differentiation and vascular growth.