Magnesium: metabolism and hormonal regulation in different species

1. The magnesium ion is of great importance in physiology by its intervention in 300 enzymatic systems, its membrane role and its function in neuromuscular excitability. 2. The skeleton is the first pool of magnesium in the animal body. 3. For intestinal absorption, renal metabolism, bone accretion and resorption, magnesium shows analogies with calcium. 4. Magnesium exchange between extracellular, cellular and skeletal compartments are very precisely controlled. 5. Parathyroid hormone, 1 alpha, 25-dihydroxy-vitamin D3, calcitonin and estrogens are the principal hormone systems implicated in magnesium metabolism. 6. The kidney is the principal site of magnesium excretion and shows important magnesium regulation mechanisms.     

The hormonal regulation of de-etiolation

De-etiolation involves a number of phenotypic changes as the plants shift from a dark-grown (etiolated) to a light-grown (de-etiolated) morphology. Whilst these light-induced, morphological changes are thought to be mediated by plant hormones, the precise mechanism/s are not yet fully understood. Here we provide further direct evidence that gibberellins (GAs) may play an important role in de-etiolation, because a similar light-induced reduction in bioactive GA levels was detected in barley (Hordeum vulgare L.), Arabidopsis (Arabidopsis thaliana L.), and pea (Pisum sativum L.). This is indicative of a highly conserved, negative-regulatory role for GAs in de-etiolation, in a range of taxonomically diverse species. In contrast, we found no direct evidence of a reduction in brassinosteroid (BR) levels during de-etiolation in any of these species. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Acceleration of rat liver phospholipid metabolism after long-term cadmium administration

Male Wistar rats, 6 weeks old, were allowed free access to water containing cadmium chloride at a concentration of 250 ppm as cadmium (Cd) for 6 and 12 months. The growth, as measured by body weight of Cd-treated rats, was significantly retarded. Electron microscopic studies revealed the appearance of small vacuoles in the cytoplasm, and involution of the rough endoplasmic reticulum (RER) in both the liver and whole kidney. When radioactive precursors of phospholipids, H3(32)PO4 and [1(3)-H]glycerol, were injected (ip) into cd-treated rats, the incorporation of 32P into phosphatidylcholine (PC) in the liver was increased 3.2- and 5.8-fold after 6- and 12-month Cd administration, respectively, and that of 3H into PC was also increased 2.3- and 2.2-fold after 6- and 12-month Cd administration, respectively. In the kidney, however, the incorporation rates of these radioactive precursors were little affected by long-term Cd administration. In the liver of rats treated with Cd for 6 and 12 months, the activity of CDP-choline:cholinephosphotransferase was increased by 20-30% over the control. It was shown that de novo synthesis of PC, which is a major constituent of biological membranes, was accelerated by long-term Cd administration in the liver but not in the kidney. These results suggest the possibility of regenerating the membranes in damaged hepatocytes after 6 and 12 months of Cd administration.     

Circadian regulation of phospholipid metabolism in retinal photoreceptors and ganglion cells

The neural retina is a key component of the vertebrate circadian system that is responsible for synchronizing the central circadian pacemaker to external light-dark (LD) cycles. The retina is itself rhythmic, showing circadian cycles in melatonin levels and gene expression. We assessed the in vivo incorporation of 32P-phosphate and 3H-glycerol into phospholipids of photoreceptor cells (PRCs) and retina ganglion cells (GCs) from chicks in constant illumination conditions (dark: DD or light: LL) over a 24-h period. Our findings showed that in DD there was a daily oscillation in 32P-labeling of total phospholipids synthesized in GCs and axonally transported to the brain. This metabolic fluctuation peaked during the subjective night (zeitgeber time [ZT] 20), persisted for several hours well into the subjective day and declined at subjective dusk (ZT 10-12). PRCs also exhibited an in vivo rhythm of 32P-phospholipid synthesis in DD. This rhythm peaked around ZT 22, continued a few hours into the day and declined by the end of subjective dusk. The major individual species labeled 1 h after 32P administration was phosphatidylinositol (PI) in both PRCs and GCs. Rhythmic phospholipid biosynthesis was also observed in DD after 3H-glycerol administration, with levels in GCs elevated from midday to early night. PRCs exhibited a similar rhythmic profile with the lowest levels of labeling during midnight. Phosphatidylcholine (PC) accounted for the individual species with the highest ratio of 3H-glycerol incorporation in both cell populations at all phases examined. By contrast, in LL the rhythm of 3H-glycerol labeling of phospholipids damped out in both cell layers. Our findings support the idea that, in constant darkness, the metabolism of retinal phospholipids, including their de novo biosynthesis, is regulated by an endogenous circadian clock.     

The hormonal regulation of purine nucleotide turnover. Influence of testosterone in rat liver

An influence of testosterone on de novo purine nucleotide synthesis has been demonstrated in rat liver of adult and prepubertal castrated rats, showing that the action of the hormone is not limited to sexual organs. Castration accelerated the turnover of purine nucleotides in adults rats and reduced it in prepubertal castrated rats. Administration of testosterone tended to restore normality in both cases with opposite mechanisms, lowering the reaction rates in the first group, enhancing them in the second one. An action of the hormone on the inosinic branch-point and specifically on GMP synthesis, was evident, which was again different according to the age of the animal. The observed changes in purine nucleotide metabolism could be responsible for variations in RNA and DNA metabolism, in cellular size and number--which probably occur in the liver--after orchiectomy and following androgen administration.     

The role of haem in the regulation of rat liver tryptophan metabolism.

Anion-exchange h.p.l.c. analysis of [3H]inositol phosphates derived from glucose-stimulated isolated pancreatic islets that had been prelabelled with myo-[3H]inositol revealed that the predominant inositol trisphosphate was the 1,3,4-isomer [Ins(1,3,4)P3]. The 1,4,5-isomer [Ins(1,4,5)P3] was also detectable, as was a more polar inositol phosphate with the chromatographic properties of inositol 1,3,4,5-tetrakisphosphate [Ins(1,3,4,5)P4]. Glucose-induced accumulation of Ins(1,3,4)P3 was augmented by Li+ and occurred after maximal accumulation of Ins(1,4,5)P3. These findings suggest a possible role for Ins(1,3,4)P3 or its probable precursor Ins(1,3,4,5)P4 in stimulus-secretion coupling in pancreatic islets.     

Surfactant phospholipid metabolism

Pulmonary surfactant is essential for life and is composed of a complex lipoprotein-like mixture that lines the inner surface of the lung to prevent alveolar collapse at the end of expiration. The molecular composition of surfactant depends on highly integrated and regulated processes involving its biosynthesis, remodeling, degradation, and intracellular trafficking. Despite its multicomponent composition, the study of surfactant phospholipid metabolism has focused on two predominant components, disaturated phosphatidylcholine that confers surface-tension lowering activities, and phosphatidylglycerol, recently implicated in innate immune defense. Future studies providing a better understanding of the molecular control and physiological relevance of minor surfactant lipid components are needed. This article is part of a Special Issue entitled Phospholipids and Phospholipid Metabolism.