Nutritional and endocrine modulation of intracellular calcium: Implications in obesity, insulin resistance and hypertension

Abstract

Regulation of intracellular Ca²⁺ ([Ca²⁺]_i) plays a key role in obesity, insulin resistance and hypertension, and [Ca²⁺]_i disorders may represent a fundamental factor linking these three conditions. We have shown insulin to be a direct vasodilator, attenuating voltage-gated Ca²⁺ influx and stimulating Ca²⁺-ATPase transcription via a glucose-6-phosphate response element. These result in a net decrease in [Ca²⁺]_i and thereby decrease vascular resistance, while these effects are blunted in insulin resistance, leading to increased vascular resistance. Consistent with this concept, pharmacological amplification of peripheral insulin sensitivity results in reduced arterial pressure. While insulin regulates [Ca²⁺]_i, Ca²⁺ also regulates insulin signaling, as increasing [Ca²⁺]_i impairs insulin signaling in some systems, possibly due to Ca²⁺ inhibition of insulin-regulated dephosphorylation. Finally, in recent studies of the mouse agouti gene, we have also demonstrated increased [Ca²⁺]_i to play a key role in adipocyte lipogenesis, as follows. We have found dominant agouti mutants to exhibit increased [Ca²⁺]_i in most tissues, leading to increased vascular reactivity and insulin resistance in vascular smooth muscle and skeletal muscle cells, respectively. Further, we have found recombinant agouti protein to directly increase [Ca²⁺]_i in a variety of cells, including murine and human adipocytes, and to stimulate both the expression and activity of adipocyte fatty acid synthase and increase triglyceride accumulation in a Ca²⁺-dependent manner. These effects can be mimicked by stimulation of Ca²⁺ influx and blocked by Ca²⁺ channel inhibition, while treatment of mice with a Ca²⁺ antagonist attenuates agouti-induced obesity. Since humans express agouti in adipose tissue, it may similarly exert paracrine effects on [Ca²⁺]_i and thereby stimulate de novo lipogenesis and promote obesity. Thus, Ca²⁺ signaling represents a target for therapeutic intervention in obesity as well as hypertension and insulin resistance. (Mol Cell Biochem 188: 129–136, 1998)