Zinc and Acrodermatitis Enteropathica

1980 ◽  
Vol 2 (3) ◽  
pp. 88-94

Mammalian zinc metalloenzymes include alkaline phosphatase. Zinc plays a crucial role in nucleic acid metabolism. RNA and DNA polymerases and thymidine kinase are zinc-dependent enzymes. Zinc deficiency in North America is most clearly seen in the disease acrodermatitis enteropathica. This is an autosomal recessive disease due to a zinc metabolic error—not well defined—which leads to zinc deficiency. Clinical manifestations include a rash around orifices, alopecia, and diarrhea. The laboratory can demonstrate hypozincemia and hypozincuria. Clinical and biochemical remission occurs with oral zinc administration.(R.H.R.)

2020 ◽  
Vol 35 (6) ◽  
pp. e201-e201
Author(s):  
Asma Al Naamani ◽  
Tuqa Al Lawati

Acrodermatitis enteropathica is a rare autosomal recessive disease caused by a genetic mutation leading to zinc deficiency. Clinical manifestation includes skin lesions, diarrhea, and alopecia. We report the case of a two-month-old girl, admitted with erythematous scaly lesions in the neck and vesiculopustular lesions in the perioral region, associated with alopecia and diarrhea. Clinical diagnosis of the disease was made from her first presentation. She was started on zinc therapy and her lesions resolved entirely after one month of treatment.


1965 ◽  
Vol 32 (3) ◽  
pp. 303-312 ◽  
Author(s):  
R. C. IMRIE ◽  
T. R. RAMAIAH ◽  
F. ANTONI ◽  
W. C. HUTCHISON

SUMMARY Treatment of female rats with adrenocorticotrophin (ACTH) increased the RNA content of the adrenal glands progressively during a period of 3 days, the DNA content increased only after prolonged administration. By contrast, ACTH caused a decrease in the uptake of [32P]orthophosphate into the total RNA of the gland and into most of the RNA fractions of the subcellular components. A method of analysis for RNA and DNA based on the Schmidt-Thannhauser procedure has been evolved which eliminates extraction of nucleic acid by lipid solvents.


1957 ◽  
Vol 106 (5) ◽  
pp. 641-648 ◽  
Author(s):  
H. F. Maassab ◽  
Philip C. Loh ◽  
W. Wilbur Ackermann

The RNA and DNA contents of the nucleus and cytoplasm of the HeLa cell were determined. The rates of incorporation of P32 into the various nucleic acid fractions were established for the ordinary HeLa cell maintained under a set of standard conditions. The changes in the rates of incorporation of P32 and in the amounts of RNA and DNA which occurred subsequent to infection with poliovirus were followed throughout the infectious cycle. These changes were correlated with the intracellular appearance of the newly formed virus. A net synthesis of RNA occurred in the cytoplasmic component of the cell. The increase was detectable 2 hours before the first appearance of demonstrable virus and reached a maximum (2.5 times normal) at 6 hours. Viral increase was not maximal before the 7th hour after infection.


1964 ◽  
Vol 47 (1) ◽  
pp. 85-94
Author(s):  
W. de Loecker

ABSTRACT Normal and hepatoma bearing rats were treated with cortisol in order to study the effect of adrenal steroids on nucleic acid metabolism of different tissues. Normal liver, precancerous liver, hepatoma nodules and skeletal muscle were used in these experiments. The incorporation of 14C from glycine-2-14C into RNA and DNA fractions of different tissues was examined. The incorporation of glycine carbon into RNA of normal and precancerous liver was found to be stimulated by cortisol treatment. The RNA fraction of hepatoma tissue of non treated animals showed a higher incorporation level than that observed in liver, but incorporation was drastically inhibited by cortisol. The DNA fraction of hepatoma tissue showed a higher incorporation than the DNA fraction from the other tissues examined, and followed the same incorporation pattern as RNA. The incorporation of 14C into the nucleic acids of skeletal muscle was not affected by cortisol treatment.


1969 ◽  
Vol 23 (3) ◽  
pp. 657-663 ◽  
Author(s):  
Ajay K. Chatterjee ◽  
Amitabha D. Roy ◽  
B. B. Ghosh

1. The effect of riboflavine deficiency on liver ribonuclease activity, RNA and DNA content, and 32P incorporation into RNA and DNA has been studied in rats maintained on a 16% protein diet, a protein-free diet and on a protein-free diet subsequently replaced with a 40% protein diet.2. Rats maintained on a riboflavine-deficient diet for 45 days showed decreased incorporation of 32P into liver RNA but no effect on the RNA content of liver. The concentration of DNA in liver and 33P incorporation into it remained unaffected. After a deficiency period of 70 days, both the RNA and DNA contents of liver were found to be decreased. When the riboflavine-deficient or control rats were given the protein diet for 30 days and then a proteinfree diet for 15 days, the RNA content of their livers decreased, while the liver DNA content was increased. Repletion with a 40% protein diet restored the RNA and DNA content in both control and riboflavine-deficient rats.3. Liver ribonuclease activity was decreased after a deficiency period of 45 days, whereas it was increased after a deficiency period of 70 days.4. A correlation between liver RNA level and liver ribonuclease activity in riboflavine deficiency is suggested.


1969 ◽  
Vol 23 (3) ◽  
pp. 671-682 ◽  
Author(s):  
A. B. Mcallan ◽  
R. H. Smith

1. Procedures, based on those of Schmidt & Thannhauser (1945) and Schneider (1945), for the extraction and estimation of nucleic acids in bovine digesta were examined in detail.2. Final methods which were suitable for routine determination of RNA and DNA were essentially as follows. Digesta samples were extracted in the cold, first with a solution of trichloroacetic acid in ethanol, then with aqueous trichloroacetic acid solution and finally with lipid solvents. The dried residue was hydrolysed with alkali, purified by passage through a Dowex resin, and the RNA, in the form of mononucleotides, determined by U.V. absorption. DNA was determined separately in hot perchloric acid extracts of the original dried residue by colorimetric estimation of the deoxyribose content.


Author(s):  
A. V. Goryainova ◽  
P. V. Shumilov ◽  
N. Yu. Kashirskaya ◽  
S. Yu. Semykin

The article considers the issue of cystic fibrosis – a monogenic autosomal recessive disease. It describes the history of the CFTR gene discovery, the further search for modifier genes to explain the variability of the clinical manifestations of cystic fibrosis. The review discusses problems of connective tissue dysplasia and somatic pathology, which is formed due to the connective tissue dysmorphogenesis in patients with cystic fibrosis; and also the article contains justification for the connection between the formation of severe fibrosis of the lungs and liver and the presence of clinical and genetic markers of connective tissue dysplasia. The author assumes that the clinical and genetic polymorphisms of connective tissue influence the course of cystic fibrosis, formation of bronchiectasis, interstitial pneumofibrosis, cystic fibrosis dysplasia, liver fibrosis and cirrhosis.


Author(s):  
G. V. Volynets ◽  
A. V. Nikitin

Alpha-1-antitrypsin deficiency is an autosomal recessive disease characterized by both liver damage and lung disease in children and adults because of a decrease in the serum protein content due to the mutations in the PI (proteinase inhibitor) gene. The majority of liver diseases are associated with a homozygous mutation of the Z allele. There are many variations of clinical manifestations of the liver disease in children with the PI*ZZ genotype.  In the neonatal period, liver disease is usually cholestatic; and it is accompanied by a prolonged cholestatic jaundice, skin itching, which can be determined only later (after 6 months), decreased appetite and bad weight gain, hepato- and splenomegaly. The article describes the pathophysiology of liver damage in children with alpha-1-antitrypsin deficiency. The authors provide their recommendations for the management of children with suspected and confirmed alpha-1-antitrypsin deficiency.


1971 ◽  
Vol 25 (1) ◽  
pp. 181-190 ◽  
Author(s):  
R. H. Smith ◽  
A. B. Mcallan

1. Concentrations of nucleic acid nitrogen and other nitrogenous constituents were estimated in digesta taken from the proximal duodenum of calves which were given, either, one of a number of stall diets or pasture. These concentrations were compared, using polyethylene glycol (PEG) as a non-absorbed marker, with corresponding concentrations in rumen fluid and ileal contents.2. There was little net change in amounts of RNA or DNA between rumen and duodenum relative to PEG, but there was a marked increase in amounts of total-N. In duodenal digesta, for any one animal given most diets, nucleic acid-N formed a fairly constant percentage (8–11 for different animals) of the total non-ammonia-N. This value was lower (by about 3) than the corresponding percentage in rumen fluid. Comparison of nucleic acid-N: total-N ratios in duodenal contents and bacteria suggested that, for these diets, about 40–55% of the non-ammonia-N in duodenal contents was of microbial origin.3. During passage of digesta between the duodenum and ileum the mean percentage disappearances of total-N, RNA and DNA were estimated to be about 67, 85 and 75 respectively. There was evidence that these values varied with the amounts of the constituents entering the duodenum.4. Ammonia was absorbed in the omasum-abomasum only when concentrations in rumen fluid were high (40 mM), but even moderate concentrations of ammonia entering the duodenum (3 mM) were efficiently absorbed (about 90%) in the small intestine.


Weed Science ◽  
1970 ◽  
Vol 18 (1) ◽  
pp. 1-4 ◽  
Author(s):  
S. S. Malhotra ◽  
J. B. Hanson

The changes in the nucleic acid metabolism were studied in plants susceptible and resistant to 4-amino-3,5,6-trichloropicolinic acid (picloram). The total RNA and DNA content of the tissue correlated inversely with the herbicide resistance; the resistant plants were low in nucleic acids, whereas sensitive plants were high. The increase in the nucleic acids of the sensitive species 24 hr after picloram treatment appeared to be associated with lower levels of ribonuclease and deoxyribonuclease. The inability of the resistant species to make more RNA may be associated with high levels of nucleases in the tissue.


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