scholarly journals Bile acids of snakes of the subfamily Viperinae and the biosynthesis of C-23-hydroxylated bile acids in liver homogenate fractions from the adder, Vipera berus (Linn.)

1976 ◽  
Vol 153 (2) ◽  
pp. 343-350 ◽  
Author(s):  
S Ikawa ◽  
A R Tammar

1. Analysis of bile salts of four snakes of the subfamily Viperinae showed that their bile acids consisted mainly of C-23-hydroxylated bile acids. 2. Incubations of 14C-labelled sodium cholate (3 α, 7 α, 12 α-trihydroxy-5 β-cholan-24-oate) and deoxycholate (3 α, 12 α-dihydroxy-5 β-cholan-24-oate) with whole and fractionated adder liver homogenates were carried out in the presence of molecular oxygen and NADPH or an NADPH-generating system. The formation of C-23-hydroxylated bile acids, namely bitocholic acid (3 α, 12 α, 23xi-trihydroxy-5 β-cholan-24-oic acid) and 3 α, 7 α, 12 α, 23 ξ-tetrahydroxy-cholanic acid (3 α, 7 α, 12 α, 23 ξ-tetrahydroxy-5 β-cholan-24-oic acid), was observed mainly in the microsomal fraction and partly in the mitochondrial fraction. 3. Biosynthetic pathways of C-23-hydroxylated bile acids are discussed.

1954 ◽  
Vol 32 (1) ◽  
pp. 383-394 ◽  
Author(s):  
Claude Allard ◽  
Gaston de Lamirande ◽  
Hugo Faria ◽  
Antonio Cantero

Acid phosphatase or phosphomonoesterase II activity of rat and mouse liver homogenates, prepared in 0.25 M sucrose, was found mainly in the cytoplasmic granules. Since the small percentage of activity of the nuclear fraction activity could be explained by the presence of mitochondria (which were actually counted in this fraction) it is concluded that rat and mouse liver nuclei do not contain acid phosphatase activity.A rather broad range of acid phosphatase activity was observed in rat and mouse livers depending on the time elapsed between the preparation of homogenate and the activity determinations. However, a preincubation of the tissues or isolated fractions at 37° C. for 60 min. was sufficient to increase the activity to an optimal value, and thus eliminate variations due to the latency of this enzyme.Alkaline phosphatase or phosphomonoesterase I activity was also found to be latent in rat liver homogenates. The phenomenon was less apparent than for acid phosphatase and seemed to depend mostly on the nature of the buffer employed in the assay system.Some evidence for the presence of two forms of alkaline phosphatase in rat liver cells is presented. One form of the enzyme was found to have an absolute requirement of magnesium for activity and was present in the soluble fraction, whereas the other which was not activated by magnesium seemed firmly linked to the nuclei and microsomes and was absent in the soluble fraction. The activity in the mitochondrial fraction was small and seemed of doubtful significance.


1954 ◽  
Vol 32 (4) ◽  
pp. 383-394 ◽  
Author(s):  
Claude Allard ◽  
Gaston de Lamirande ◽  
Hugo Faria ◽  
Antonio Cantero

Acid phosphatase or phosphomonoesterase II activity of rat and mouse liver homogenates, prepared in 0.25 M sucrose, was found mainly in the cytoplasmic granules. Since the small percentage of activity of the nuclear fraction activity could be explained by the presence of mitochondria (which were actually counted in this fraction) it is concluded that rat and mouse liver nuclei do not contain acid phosphatase activity.A rather broad range of acid phosphatase activity was observed in rat and mouse livers depending on the time elapsed between the preparation of homogenate and the activity determinations. However, a preincubation of the tissues or isolated fractions at 37° C. for 60 min. was sufficient to increase the activity to an optimal value, and thus eliminate variations due to the latency of this enzyme.Alkaline phosphatase or phosphomonoesterase I activity was also found to be latent in rat liver homogenates. The phenomenon was less apparent than for acid phosphatase and seemed to depend mostly on the nature of the buffer employed in the assay system.Some evidence for the presence of two forms of alkaline phosphatase in rat liver cells is presented. One form of the enzyme was found to have an absolute requirement of magnesium for activity and was present in the soluble fraction, whereas the other which was not activated by magnesium seemed firmly linked to the nuclei and microsomes and was absent in the soluble fraction. The activity in the mitochondrial fraction was small and seemed of doubtful significance.


1969 ◽  
Vol 113 (2) ◽  
pp. 429-440 ◽  
Author(s):  
Elizabeth H. Shephard ◽  
G. Hübscher

1. After conventional fractionation of rat liver homogenates in 0·88m-sucrose the mitochondrial fraction was subjected to short-term water lysis followed by separation of the resulting membrane preparations. 2. Phosphatidate formation was measured in all subcellular fractions and subfractions and was compared with the distribution of succinate dehydrogenase, monoamine oxidase, rotenone-insensitive NADH cytochrome c reductase, arylsulphatase, urate oxidase, arylesterase and glucose 6-phosphatase. 3. The results obtained indicated that mitochondria were capable of synthesizing phosphatidate, though this activity was only about one-third of the total homogenate activity. 4. Mitochondrial phosphatidate formation was located predominantly in the outer mitochondrial membrane. Although this membrane preparation was found to be significantly contaminated by the microsomal fraction, this contamination was estimated to account for not more than about 20% of the total phosphatidate formation observed in preparations of outer mitochondrial membrane.


1967 ◽  
Vol 105 (2) ◽  
pp. 505-513 ◽  
Author(s):  
V. N. Nigam ◽  
A. Fridland

Liver homogenates of avian species, but not of mammals, form glycogen from glucose, mannose, fructose and galactose. Incorporation of labelled glucose, fructose and mannose, but not of labelled galactose, into glycogen is diluted isotopically by unlabelled glucose. Except for fructose, glycogen formation from other substrates by pigeon liver homogenates compares favourably with that from the same substrates in pigeon liver slices. Optimum conditions for glycogen synthesis from glucose by pigeon liver homogenate are: medium of incubation, 0·175m-sucrose–45mm-potassium chloride−15mm-glycylglycine buffer, pH 7·5; concentration of substrate, 15mm; concentration of tissue, less than 120mg./ml.; temperature of incubation, 37–43°; atmosphere, oxygen. Uncouplers of oxidative phosphorylation, Ca2+, EDTA, PPi, 2-deoxyglucose 6-phosphate and microsomal fraction of rat liver are inhibitory to glycogen synthesis from glucose. Starvation of pigeons for 24 and 48hr. leads to a slight stimulation of glycogen synthesis in their liver homogenates as compared with fed controls. Pigeon liver homogenates can be separated into subcellular fractions that on reconstitution can synthesize glycogen. All the enzymes of the glycogen pathway except soluble high-Km glucokinase are present in pigeon liver.


Author(s):  
O. V. Lototska

Toxic effects of heavy metals on animals and humans is aggravating the presence of surfactants. The aim of our research was to identify the peculiarities of free radical oxidation and antioxidant protection in the use of drinking water with subtoxic doses of potassium and sodium stearates in combination with copper on the body of warmblooded animals, such as the liver of experimental rats. Analysis of indicators allows asserting that in experimental rats liver homogenate observed activation of free radical oxidation, the intensity of which depended on the concentration of stearates in water. More pronounced changes were in animals that consumed water with potassium stearate.The action of potassium stearate observed inhibition of antioxidant systems while under the influence of sodium stearate – its activation. Changes in performance were more pronounced in combination stearates with copper.


In this work the bile acids and certain of their derivatives have been studied with regard to their bacteriostatic power and relative activities in removing the Gram-positive complex from yeast. No correlation between these properties was obtained. A simple relationship was apparent, however, between the bacteriostatic activities of the compounds and their ability to depress the surface tension of the metabolism medium. The limiting dilution at which the 'active' bile acids were bacteriostatic for Staphylococcus aureus corresponded to a depression of the surface tension of the medium by approximately 4∙5 dynes. The relationship between bacteriostatic power and surface activity was only valid for this particular series of compounds of closely related molecular structure.


2006 ◽  
Vol 27 (5-6) ◽  
pp. 1248-1254 ◽  
Author(s):  
Carmem Dickow Cardoso ◽  
Valquíria A. Polisel Jabor ◽  
Pierina Sueli Bonato

1955 ◽  
Vol 33 (2) ◽  
pp. 135-138 ◽  
Author(s):  
B. B. Migicovsky

The inability of liver homogenates, from starved and vitamin A deficient rats, to synthesize cholesterol is illustrated. A possible reason for this phenomenon is that these preparations inhibit cholesterol synthesis when added to a liver homogenate from a normal rat. The inhibitory factor or factors are present in both the supernate and residue portions of the homogenate, although the residue matter is more inhibitory.


2020 ◽  
Author(s):  
Bojana R. Vasiljević ◽  
Edward T. Petri ◽  
Sofija S. Bekić ◽  
Andjelka S. Ćelić ◽  
Ljubica M. Grbović ◽  
...  

Green synthesis of bile acids derivatives and 5β-cholanic acid was achieved under microwave irradiation, and the binding affinity for the ligand binding domain of the glucocorticoid receptor was measured.


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