Studies on the Chemical Composition of Muscle Tissue

1961 ◽  
Vol 38 (4) ◽  
pp. 707-728
Author(s):  
JAMES D. ROBERTSON

1. Comprehensive analyses have been made of the muscle and plasma for inorganic ions, organic phosphates, soluble carbohydrates, amino acids and nitrogenous bases. 2. Compared with a total of 1108 mg. ions/kg. water in the plasma, the muscle had 1045, of which 515 were mg. ions (Na, K, Ca, Mg, Cl, SO4, lactate, HCO3, inorganic and arginine phosphates, adenosine triphosphate, hexose phosphates, etc.), and the remainder amino acids (405 mM.) and the nitrogenous compounds trimethylamine oxide (59 mM.) and betaine (66 mM.). 3. Measurements of the apparent extracellular spaces in the muscle following injections of inulin, sucrose and sodium thiosulphate have led to the conclusion that the inulin space or permeation, 12.1%±0.69 (S.E.) of the total muscle water, is the best indication of total extracellular fluid in the muscle. The copper space, 4.11±0.37, represents a maximum value for the blood space (that filled with haemocyanin), leaving 8.0% as the volume occupied by interstitial fluid. 4. Intracellular concentrations of potassium and chloride do not conform to values expected on the basis of a Donnan equilibrium with plasma: [Ki]/[Ko] = 21.9, [Clo]/[Cli] = 9.9. 5. Mean values in mg. ions/kg. water for the whole muscle concentrations of phosphate ions are inorganic phosphate 18.3, arginine phosphate 71.0, adenosine triphosphate 11.6, remaining acid-soluble phosphate, chiefly hexose phosphates, 14.4, total 115.2. 6. Total non-protein amino acids of muscle from measurements of α-amino N are 339-551 mM., mean 476. These are chiefly glycine, proline, arginine, taurine, alanine and glutamine. Most of the arginine is combined as arginine phosphate. 7. Direct measurements of osmolality of the plasma using Krogh-Baldes thermocouples give a mean value of 100.4±0.34 (N = 9), taking sea water as 100. Measurements of the juice expressed from muscle with a tissue-press give a mean value compared with plasma (100) of 102.0±0.70 if done within 1.5 hr. of removing the muscle, 101.7±0.87 for seven estimations done within an hour; the latter result is not significantly different from the plasma values. Delay in measurement leads to higher values (plus 5-8% on plasma), owing to the breakdown of labile compounds. 8. Compared with whole muscle on a water-content basis, the concentrations of ions in the muscle-juice are Na 76%, K 74%, Ca 10%, Mg 40%, Cl 100%, total acid-soluble P 78%. This is interpreted as showing binding by proteins of fractions of all these ions except chloride. If the juice is corrected for its extracellular component, approximate percentages of ions bound inside the muscle cells are Na 82%, K 26%, Ca 100%, Mg 64% and P 22% all the cellular chloride is free. 9. A final osmotic balance sheet for Nephrops muscle cells, in which consideration has been given to such factors as binding of ions, osmotic coefficients of ions and probable ideal behaviour of the nitrogenous compounds, shows that about 92% of the total osmotic concentration (in milliosmoles) has been accounted for. 10. Increasing the concentration of potassium and calcium in sea water leads to increases in the values of these ions in both plasma and muscle.

2020 ◽  
Vol 21 (8) ◽  
pp. 785-798 ◽  
Author(s):  
Abedin Abdallah ◽  
Evera Elemba ◽  
Qingzhen Zhong ◽  
Zewei Sun

The gastrointestinal tract (GIT) of humans and animals is host to a complex community of different microorganisms whose activities significantly influence host nutrition and health through enhanced metabolic capabilities, protection against pathogens, and regulation of the gastrointestinal development and immune system. New molecular technologies and concepts have revealed distinct interactions between the gut microbiota and dietary amino acids (AAs) especially in relation to AA metabolism and utilization in resident bacteria in the digestive tract, and these interactions may play significant roles in host nutrition and health as well as the efficiency of dietary AA supplementation. After the protein is digested and AAs and peptides are absorbed in the small intestine, significant levels of endogenous and exogenous nitrogenous compounds enter the large intestine through the ileocaecal junction. Once they move in the colonic lumen, these compounds are not markedly absorbed by the large intestinal mucosa, but undergo intense proteolysis by colonic microbiota leading to the release of peptides and AAs and result in the production of numerous bacterial metabolites such as ammonia, amines, short-chain fatty acids (SCFAs), branched-chain fatty acids (BCFAs), hydrogen sulfide, organic acids, and phenols. These metabolites influence various signaling pathways in epithelial cells, regulate the mucosal immune system in the host, and modulate gene expression of bacteria which results in the synthesis of enzymes associated with AA metabolism. This review aims to summarize the current literature relating to how the interactions between dietary amino acids and gut microbiota may promote host nutrition and health.


1984 ◽  
Vol 2 (1) ◽  
pp. 11-21 ◽  
Author(s):  
James Braven ◽  
Roger Evens ◽  
E. Ian Butler
Keyword(s):  

Author(s):  
E. D. S. Corner ◽  
B. S. Newell

A study has been made of the nitrogenous compounds excreted by Calanus helgolandicus (Claus) collected at Plymouth.Most of the excreted nitrogen is in the form of ammonia which accounts for 60–100% (average 74.3%) of the total, and some of the remainder may be lost as urea. There is no evidence for the excretion of measurable amounts of amino acids.Whether the animals are starved or fed they are primarily ammonotelic, and the quantity of ammonia produced at 10° C (3.33 μg/g. dry body wt/day) is not significantly changed when the animals are used at an abnormally high experimental density. This latter condition does, however, lead to the production of large quantities of additional nitrogenous substances that give a positive reaction with ninhydrin.IntroductionThe amounts of nitrogen excreted by zooplankton have been measured by several workers. Harris (1959) used the method of Riley (1953) to estimate the copious quantities of ammonia produced by animals (mainly Acartia tonsa and A. clausi) collected from Long Island Sound; Beers (1964), in laboratory experiments with the chaetognath Sagitta hispida, estimated the excreted ammonia by the procedure of Kruse & Mellon (1952); and Corner, Cowey & Marshall (1965) determined the ammonia excreted by Calanus helgolandicus and C. finmarchicus, using a ninhydrin technique described by Moore & Stein (1954). The methods employed by Harris and by Beers are specific for ammonia: that used by Corner et al. estimates nitrogenous substances (e.g. amino acids) in addition to ammonia, but certain tests were made which seemed to exclude the possibility that these substances contributed significantly to the nitrogen excreted by the animals.


2011 ◽  
Vol 2011 ◽  
pp. 1-6
Author(s):  
Ramón A. Lorca ◽  
Lorena Varela-Nallar ◽  
Nibaldo C. Inestrosa ◽  
J. Pablo Huidobro-Toro

Although the physiological function of the cellular prion protein (PrPC) remains unknown, several evidences support the notion of its role in copper homeostasis. PrPCbinds Cu2+through a domain composed by four to five repeats of eight amino acids. Previously, we have shown that the perfusion of this domain prevents and reverses the inhibition by Cu2+of the adenosine triphosphate (ATP)-evoked currents in the P2X4receptor subtype, highlighting a modulatory role for PrPCin synaptic transmission through regulation of Cu2+levels. Here, we study the effect of full-length PrPCin Cu2+inhibition of P2X4receptor when both are coexpressed. PrPCexpression does not significantly change the ATP concentration-response curve in oocytes expressing P2X4receptors. However, the presence of PrPCreduces the inhibition by Cu2+of the ATP-elicited currents in these oocytes, confirming our previous observations with the Cu2+binding domain. Thus, our observations suggest a role for PrPCin modulating synaptic activity through binding of extracellular Cu2+.


1966 ◽  
Vol 13 (6) ◽  
pp. 1115-1124 ◽  
Author(s):  
Y.K. Chau ◽  
J.P. Riley
Keyword(s):  

1971 ◽  
Vol 178 (1050) ◽  
pp. 111-129 ◽  

When symbiotic coelenterates, especially hermatypic corals, were incubated in the light in sea water containing NaH 14 CO 3 , small quantities of fixed 14 C were released from the tissues at a steady rate over 4 h. The rate of release was greatly increased in the presence of glycerol, glucose and alanine; the additional 14 C released was in the same substance as that added to the medium. The following related compounds had little or no effect on 14 C release : ethylene glycol, sorbose, fructose, glucosamine, glycine, proline, serine and glutamic acid. Such results have been previously reported in other symbiotic systems, and the substances causing the specific release of fixed 14 C are believed to be those which move from the autotrophic to the heterotrophic symbiont. This belief is supported here by previous observations that glycerol, glucose and alanine are among the most important organic substances released by freshly isolated zooxanthellae. Ammonium chloride increased the amount of fixed 14 C released by corals into alanine media, possibly due to conversion of ammonia to amino acids by zooxanthellae. Appreciable release of 14 C fixed in the dark also occurred into alanine solutions. These results suggest possible roles of zooxanthellae in supplying organic nitrogen compounds to the host cell at night as well as during the day. The involvement of zooxanthellae in ‘recycling’ nitrogen compounds within the association may help to explain the success of corals in seas poor in nutrients. There was substantial utilization of external glycerol and glucose when supplied at either high or low concentrations. Corals may well be able to utilize some of the small amounts of organic matter dissolved in sea water in the natural environment.


1962 ◽  
Vol 39 (3) ◽  
pp. 345-352
Author(s):  
H. BARNES

1. The results of some chemical analyses for inorganic and organic constituents of the seminal plasma of Balanus balanus are presented. 2. The inorganic ions show a cation deficit of 178 m-equiv./l., which is probably made up by free amino-acids. 3. Cystine is a prominent amino acid present. 4. Potassium and calcium are present in excess of their quantities in sea water. 5. Reducing sugars, compared with the amount found in sea-urchin spermatozoa, are found in moderate quantities, 1 mg./ml. 6. Phosphorus of all kinds is present in only small quantities (total of o.14 mg./ml.). 7. Some phosphatases are present. 8. There are 21 /µg./ml. of ascorbic acid; the function of this is discussed in relation to its possible contribution to the protective action against the poisoning of -SH groups by thiol-reactive agents.


1968 ◽  
Vol 3 (4) ◽  
pp. 515-527
Author(s):  
J. PIATIGORSKY ◽  
A. TYLER

Unfertilized and fertilized eggs of the sea urchin Lytechinus pictus were preloaded with [14C]valine and exposed to individual solutions of each of the twenty ‘coded’ [12C]amino acids in artificial sea water. After 1 h incubation the amount of radioactivity in the medium was determined. The radioactivity was effectively displaced by most of the other neutral [12C]amino acids that are known to compete with valine for uptake. A chromatographic test with fertilized eggs showed the displaced radioactivity to be [14C]valine and not some metabolic product. Addition of acidic, basic or some neutral amino acids that are known to be poor inhibitors of valine uptake did not cause significant quantities of label to appear in the medium. For the unfertilized eggs, the concentration of acid-soluble label remained many hundreds of times greater in the egg fluid than in the sea water. Tests indicated that efflux of [14C]valine and subsequent competition for re-entry is a primary factor responsible for the displacement phenomenon. That this may not be the sole factor is suggested by the fact that some amino acids that are known to be powerful inhibitors of valine uptake were found to be only weak displacers of [14C]valine. Neither [14C]arginine nor [14C]glutamic acid were displaced in significant amounts from preloaded unfertilized or fertilized eggs by any of the tested [12C]amino acids. Attempts were made to utilize the displacement of [12C]valine to elevate the incorporation of [14C]valine and of other labelled amino acids into protein by intact eggs. Unfertilized and fertilized eggs were pretreated with related [12C]amino acids and then exposed to [14C]valine or a mixture of [14C]amino acids. The results varied in the different tests, ranging from no significant increase to 2-fold.


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