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Cerrahpaşa Tıp Fakültesi

Prof.Dr.M.Koray GÜMÜŞTAŞ,Assoc.Prof.Dr. Karolin Yanar

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trace elements mineral metabolism biology nutrients

Summary

This document provides information on trace elements, focusing on zinc and copper, their roles in enzymes, and related metabolic processes. It discusses their functions, sources, and potential toxicity.

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Prof.Dr.M.Koray GÜMÜŞTAŞ Assoc.Prof.Dr. Karolin Yanar İUC-Cerrahpaşa MePistry Zinc (Zn) • oysters, meat, liver, wheat germ, pumpkin seeds, sunflower seeds, all grains, almonds and milk are zinc rich nutrients Functions of zinc related with involvement of enzymes structure • • • • • • • • • • Re...

Prof.Dr.M.Koray GÜMÜŞTAŞ Assoc.Prof.Dr. Karolin Yanar İUC-Cerrahpaşa MePistry Zinc (Zn) • oysters, meat, liver, wheat germ, pumpkin seeds, sunflower seeds, all grains, almonds and milk are zinc rich nutrients Functions of zinc related with involvement of enzymes structure • • • • • • • • • • Redox homeostasis (superoxide dismutase) Regulation of pH (carbonic anhydrase) Nonspecific aldehyde synthesis (alcohol dehydrogenase) Visual cycle and night vision (retinol dehydrogenase) Folate digestion (polyglutamate hydrolase) Protein digestion(carboxypeptidase A and B ) Phospholipid metabolism (phospholipase C) Hem synthesis (aminolevulunic acid dehydratase) Nucleic acid and nucleotide metabolism (DNA polymerase, RNA polymerase ) Taste (gustin) *Functions of zinc related with matrix metalloproteinases • MMPs initiate bone growth and remodeling • innate immunity, • wound repair, • angiogenesis, • tissue repair, • cell migration Other functions • Regulation of serotonin and norepinephrine content • Cellular adhesion • Sperm motility and vitality • The participation of zinc in hormone production • zinc finger Tetrahedral zinc atoms bind with histidine and cysteine residues of protein and form folded structures known as zing finger • Zinc finger play roles in transcriptional regulation, ubiquitin-mediated protein degradation, signal transduction, actin targeting, DNA repair, cell migration, tumorigenesis, cancer progression, metastasis, regulation of hormone such as free T4, thymulin, estrogen, testosterone, insulin, insulin like growth factor-1 • Daily zinc requirement is about 12-15 mg, Max; 50mg • 15-30% of ingested zinc absorbed in duedenum and upper jejenum • Intestinal Zn2+ is absorbed by carrier mediated transport and diffusion • It is carried with Albumin (%60-70)and α2-macroglobulin(30- 40%) in plasma • It is bind to metallothionein and stored that form in tissues • It is excreted by sweat, feces and urine ACRODERMATITIS ENTEROPATICA • A rare cause of impaired zinc absorption from the intestine. • A severe zinc deficiency in which whole body zinc stores are depleted • is an autosomal recessive inborn error that occurs mutation of the zip encoding gene (ZIP4) on chromosome 8q24 toxicity • Zinc is relatively nontoxic. • Gastrointestinal system tract symptoms, decrease in heme synthesis and hyperglycemia have been observed in excessive (1gram) or repetitive doses exposure of zinc for several months. • Heme synthesis is decreased due to effects of excessive zinc concentration on copper metabolism. • Excessive zinc exposure produces some symptoms as abdominal and epigastric pain, bloody diarrhea, nausea and vomiting, metallic taste, decreased immune function, alteration in copper and iron metabolism in acute conditions. • In chronic conditions it may lead to copper deficiency, numbness, weakness, ataxia, and spastic gait, sideroblastic anemia, neutropenia and hyperglycemia • Excessive levels of intracellular zinc may play a role in cellular toxicity. Ischemia-reperfusion injury and Alzheimer’s disease are related to excessive zinc levels. • Increased intracellular levels of zinc results in loss of mitochondrial membrane potential, generation of free radicals, cell death and inhibition of α -ketoglutarate dehydrogenase complex Copper • Copper- rich dietary sources are liver, kidney, shellfish, nuts, raisins, egg yolk, whole grain cereals, cacao containing products, and legumes • RDA 900 µg/day for adult *Copper is core part of copper- containing enzymes which terms as cuproenzymes Cuproenzyme Function Lysyl oxidase Indole 2,3-dioxygenase Dopamine monooxygenase Superoxide dismutase 1 izoenzyme Ceruloplasmin Collagen and elastin cross-link Tryptophan metabolism Norepinephrine synthesis Antioxidant Ferroxidase activity, chaperone binding, copper and iron transports Ferroxidase activity Melanin synthesis Oxidation of monoamine and diamines, detoxication of serotonin, spermidine, putresin,1 phenyl-ethylamine ATP production Hephestin Tyrosinase Amine oxidase Cytochrome c oxidase • Copper is absorbed mainly in the small intestine and slightly in stomach. • The intestinal uptake is dependent on pH. • Approximately, 40%-70% of ingested copper is absorbed • If copper content is low(lower than 1 mg/day), the absorption is around 50% whereas, if it is high around(higher than 5mg/day) 20% is absorbed *ceruloplasmin • It is synthesized in the liver. • It is an acute phase reactant. • It has ferroxidase activity. • It has antioxidant properties. • It contains 6-8 copper • Ceruloplasmin enables iron to be oxidized (Fe+3) with its ferroxidase activity and provide to bind transferrin • Normal value of serum copper level in a healthy adult is 65-165 g/dL Higher-than-normal serum copper level hypercupremia • Lower than normal serum copper level, hypocupremia *Disorders of copper metabolism • Menkes’ disease • Menkes disease (Menkes kinky hair syndrome), a progressive neurodegenerative disease with X-linked recessive inheritance starting from early childhood • Due to the mutation in the gene of the Cu+2 -carrying ATPase, the transport and storage of copper is impaired. • Low levels of plasma copper • The most important findings to support the diagnosis are hair findings. Lightening in hair color, wooly, hard and mixed hair is typical. • (Due to the loss of disulfide bond catalyzed by Cu+2------ Lysyl oxidase) If untreated, death occurs due to dysfunction of copper enzymes. *Wilson’s disease •It is a genetically determined copper accumulation disease. •. Loss- of- function mutation of gene that encodes ATP7B is lead to Wilson’s disease •Neurological disorders, liver cirrhosis, Kayser- Fleischer ring (green-brown discoloration) due to copper deposition •Copper accumulation in all tissues, especially liver, brain (Basal ganglia), cornea and kidneys Symptoms and signs Wilson cirrhosis • Serum ceruloplasmin levels are low. • Total serum copper decreased due to ceruloplasmin deficiency, but serum free copper increased. • Quantitative copper increase in liver biopsy (Gold standard in diagnosis) Copper toxicity • It can be formed by copper pots, some burn pomades and fungicides. • Bleeding in the GIS, renal dysfunction, and neurological findings are in question. manganese • Almond, apricot, bran, kidney, lentil, parsley, walnut, cress, wheat extract are manganese rich nutrients • It is absorbed through the small intestine by a mechanism similar to iron absorption. • It is found in many metalloenzyme structures in the form of Mn+2, Mn+3. • Enzymes containing Mn in their structure -arginase -Pyruvate carboxylase -Superoxide dismutase; -Transferase, - decarboxylase, -hydrolases; • Bone development; It is a cofactor of glycosyltransferase, which enables the synthesis of proteoglycans. • wound healing; in collagen and glycosaminoglycan synthesis Neuromuscular disorders and schizophrenia-like findings in manganese intoxication • Excess manganese activates atherosclerosis. • Manganese Deficiency: Irregularity in balance, infertility, decreased desire for sex, abnormal development in the body,increase birth of a dead child Chromium (Cr) • Cr +3 and Cr +6 valence forms are found in biological systems. • glucose tolerance factor • It strengthens the effects of insulin. • Facilitates the binding of insulin to its receptors • Insulin is ineffective as a glucose regulator without chromium. Chromium deficiency leads to atherosclerosis

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