Search PubMed⌕ Search

Biomedical subjects

J Ganguly

Publications and source records attributed to J Ganguly.

At least 55 records · Page 3Linked to original sources

Studies on the phospholipases of rat intestinal mucosa.

1. Subcellular distribution and characteristics of different phospholipases of rat intestinal mucosa were studied. 2. The presence of free fatty acid was necessary for the maximal hydrolysis of lecithin (phosphatidylcholine), but there was no accumulation of lysolecithin (1 or 2-acylglycerophosphorylcholine);lysolecithin accumulated when the reaction was carried out in the presence of sodium deoxycholate and at or above pH8.0. 3. The fatty acid-activated phospholipase B as well as lysolecithinase showed optimum activity at pH6.5, whereas for the phospholipase A it was about pH8.6. 4. The bulk of the phospholipase A was present in the microsomal fraction, whereas the phospholipase B and lysolecithinase activities were distributed between the microsomal and soluble fractions of the mucosal homogenate. 5. Phospholipase A was equally distributed between the brush border and brush-border-free particulate fraction, with the brush border having highest specific activity, whereas the other two activities were distributed between the brush-border-free particulate and soluble fractions. 6. Various treatments showed marked differences between the phospholipase A and phospholipase B activities, but not between phospholipase B and lysolecithinase activities. 7. By using (beta[1-(14)C]-oleoyl) lecithin it was shown that the mucosal phospholipase A was specific for the beta-ester linkage of the lecithin molecule.

Animals↗

Acylation of lysolecithin in the intestinal mucosa of rats.

1. The presence of an active acyl-CoA-lysolecithin (1-acylglycerophosphorylcholine) acyltransferase was demonstrated in rat intestinal mucosa. 2. ATP and CoA were necessary for the incorporation of free [1-(14)C]oleic acid into lecithin (phosphatidylcholine). 3. The reaction was about 20 times as fast with [1-(14)C]oleoyl-CoA as with free oleic acid, CoA and ATP. 4. With 1-acylglycerophosphorylcholine as the acceptor, both oleic acid and palmitic acid were incorporated into the beta-position of lecithin; the incorporation of palmitic acid was 60% of that of oleic acid. 5. Of the various analogues of lysolecithin tested as acyl acceptors from [1-(14)C]oleoyl CoA, a lysolecithin with a long-chain fatty acid at the 1-position was most efficient. 6. The enzyme was mostly present in the brush-border-free particulate fraction of the intestinal mucosa. 7. Of the various tissues of rats tested for the activity, intestinal mucosa was found to be the most active, with testes, liver, kidneys and spleen following it in decreasing order.

Acyltransferases↗

Studies on metabolism of vitamin A. The effect of hormones on gestation in retinoate-fed female rats.

1. Female rats, raised to maturity on a vitamin A-deficient diet supplemented with retinoate as the sole source of vitamin A, conceived when allowed to mate with normal males, but the conception resulted in foetal resorption, beginning from day 14 or 15 of pregnancy. 2. Daily injections of pregnenolone or oestradiol-17beta, but not of progesterone, were fully effective, and transplantation of pituitary homografts under kidney capsules was 80% effective, in preventing resorption. 3. Unilateral ovariectomy, leading to compensatory hypertrophy of the remaining ovary, resulted in significantly fewer corpora lutea and in lower weight of the hypertrophied ovary of the retinoate-treated rats, as compared with the corresponding retinyl acetate-fed ones. 4. The activity of the enzyme system Delta(5)-3beta-hydroxy steroid dehydrogenase was significantly less in the ovaries of the retinoate-fed rats that were subjected to unilateral ovariectomy or were made pregnant, when compared with that of the corresponding controls. Also, the ovaries of the retinoate-treated rats were insensitive to both exogenous and endogenous gonadotrophin stimulus. 5. These results indicate that one of the reasons for foetal resorption in the retinoate-fed rats might be inadequate synthesis of steroid hormones such as pregnenolone and oestrogen.

Animals↗

Studies on the positional integrity of glyceride fatty acids during digestion and absorption in rats.

1. Rats previously starved for 24hr. were separately given by intraduodenal injections 0.5ml. of a dispersion containing 10mg. of sodium taurocholate, with 50mg. of glycerol 1,3-dioleate 2[1-(14)C]-palmitate, glycerol 1,2-dioleate 3[1-(14)C]-palmitate, a mixture of [1-(14)C]palmitic acid and triolein, or a mixture of [1-(14)C]-palmitic acid and oleic acid. 2. At the end of 30min., the net amounts, and the radioactivity, of the neutral-lipid components recovered from the intestinal lumen and mucosa, and the position of the labelled palmitic acid in the mucosal triglycerides, were determined. 3. When glycerol 1,3-dioleate 2[1-(14)C]-palmitate was administered, most of the labelled acid was retained in the di- and monoglycerides of the lumen; the triglycerides were the major components containing the radioactivity in the mucosa and 75-80% of the labelled acid was located at the beta-position of these triglycerides. 4. When glycerol 1,2-dioleate 3[1-(14)C]-palmitate was administered, the labelled acid was readily split off in the lumen and virtually no radioactivity could be traced in the monoglyceride fraction; in the intestinal mucosa, triglycerides were again the chief components containing most of the radioactivity, and 80-85% of the labelled acid was esterified at the outer positions of the glycerol. 5. When [1-(14)C]palmitic acid mixed with triolein was administered, the concentrations of free fatty acids increased markedly in the intestinal lumen and mucosa, and 80-88% of the radioactivity of the mucosal triglycerides was located at the outer positions of the glycerol. 6. When [1-(14)C]palmitic acid mixed with oleic acid was administered, the labelled acid accumulated in the lumen as well as in the cell, and it was randomly incorporated into all three positions of the mucosal triglycerides.

Animals↗

Pathways of absorption of retinal and retinoic acid in the rat.

The chemical and anatomical pathways of absorption of dietary retinal, retinoic acid, and retinol were examined in rats containing lymph, bile, and duodenal cannulae. The experiments were designed to maintain physiological conditions to the greatest possible extent. In each rat an uninterrupted flow of bile into the duodenum was maintained by connecting the duodenal cannula to the bile duct of a second rat. Labeled vitamin A compounds were introduced into the duodenum in very small amounts (7-14 micrograms) in the form of a bile-lipid mixture resembling normal intestinal contents. Under these conditions, most (70-80%) of the radioactivity recovered after the feeding of labeled retinol or retinal was found in the lymph, predominantly in saturated retinyl esters. In contrast, 92-95% of the radioactivity recovered after the feeding of labeled retinoic acid was found in the bile, and was contained in a mixture of polar metabolites, most of them more polar than free retinoic acid. Two-thirds of the small amount of radioactivity found in lymph after retinoic acid-(14)C feeding was in the form of free retinoic acid. The results indicate that under normal conditions the major pathway of retinal absorption involves its reduction to retinol, which is then esterified and transported via the lymphatics in a manner similar to that of dietary retinol. A small proportion of retinal is apparently normally oxidized, and is then transported via the portal vein and excreted in the bile in a manner similar to that of dietary retinoic acid. The relative importance, in quantitative terms, of these two pathways of retinal metabolism can vary, depending on the status of the animal.

Animals↗

Role of the intestinal brush border in the absorption of cholesterol in rats.

1. Short-term incubation of the everted intestinal sacs of rats in media containing cholesterol oleate or cholesterol plus oleic acid resulted in rapid hydrolysis, but no synthesis, of the sterol ester. 2. On separation of the brush border from the rest of the mucosal cell, almost all of the hydrolytic activity and appreciable amounts of the synthetic activity of the whole cell were found to be present in the brush-border fraction. 3. The isolated brush-border fraction contained considerable amounts of cholesterol, which was always present in the unesterified state; the rest of the cell contained about an equal amount of unesterified cholesterol, but, in addition, small but definite amounts of the esterified sterol were also found in this fraction. 4. On feeding rats with [4-(14)C]cholesterol, which was diluted with 3mg. of cholesterol, it was found that the brush border very rapidly took up the fed sterol without changing its net content of cholesterol. No traces of radioactive cholesterol ester could ever be detected in the isolated brush border after feeding with (14)C-labelled esterified or unesterified cholesterol. 5. The appearance of the labelled sterol was quite rapid in the rest of the cell also, where small proportions were found in the esterified state. 6. Therefore the sequence of events in the absorption of cholesterol appears to be: the dietary cholesterol esters are hydrolysed by the cholesterol ester hydrolase of pancreas or of the mucosal brush border or both, after which the brush border rapidly absorbs the de-esterified sterol and transfers it into the mucosal cell, by a mechanism of displacement, where it is slowly re-esterified for transport through the lymph.

Alkaline Phosphatase↗

Studies on metabolism of vitamin A. The effect of the stage of vitamin A deficiency on sulphate activation in rat liver.

1. The synthesis of ;active sulphate' in rat liver was studied at various stages of vitamin A deficiency, with the corresponding pair-fed controls. 2. The activity was significantly decreased even at the onset of the deficiency, and at the acute stage there was further loss. 3. Only at the earlier stages of the deficiency was the addition of retinol, in vitro, fully effective in restoring the lost activity; retinoic acid was partially active. No such restoration was possible at the acute deficiency stage.

Adenine Nucleotides↗

The effect of vitamin A deficiency on the biosynthesis of steroid hormones in rats.

1. The synthesis, both in vivo and in vitro, of various steroid hormones in the adrenals, testes and ovaries of rats was compared at various stages of vitamin A deficiency with the corresponding pair-fed controls. 2. The enzymic conversion of the Delta(5)-3beta-hydroxy steroids into the corresponding Delta(4)-3-oxo steroids was significantly decreased in these tissues even at the mild-deficiency stage, further loss taking place on prolonging the deficiency. 3. In all three tissues the loss in the production of androstenedione from dehydroepiandrosterone could be reactivated in vitro by retinol or retinoic acid, but only at the mild stage of the deficiency. 4. Of the various lipoidal materials tried, retinal, retinol, retinoic acid, alpha-tocopherol acetate, menadione, calciferol, lecithin, palmitic acid and cholesterol, only retinol and retinoic acid restored the lost activity. 5. Intraperitoneal injection of retinal, retinol or retinoic acid into the deficient rats, 24hr. before they were killed, corrected the effect of the deficiency on this reaction. 6. Vitamin A deficiency markedly affected the synthesis of deoxycorticosterone and corticosterone from pregnenolone in the adrenals of rats, even at the mildly deficient stage, with further loss taking place at the acute stage; in vitro, retinol or retinoic acid could restore the loss at the mild-deficiency but not at the acute-deficiency stage. 7. The deficiency had no such effect on the synthesis of deoxycorticosterone from progesterone or of corticosterone from progesterone or deoxycorticosterone. 8. Compared with the pair-fed normals, the adrenals of deficient rats contained smaller amounts of deoxycorticosterone and corticosterone.

Adrenal Glands↗

Studies on metabolism of vitamin A. Absorption of retinal (vitamin A aldehyde) in rats.

1. Young rats with low reserves of vitamin A were dosed with retinal in groundnut oil, and the stomach, the contents, mucosa and muscles of small intestine, the blood and the liver were analysed at periods up to 24hr. after dosing. 2. Up to 6hr. after the dose, retinal was present in high concentrations in the contents, mucosa and muscles of the intestine. Small but significant amounts were present in blood and liver at all times. 3. The intestinal mucosa and muscles always contained small amounts of retinol and its esters. 4. A study of the distribution of the three forms of the vitamin within the mucosal cell showed that most of the mucosal retinal enters the cell unchanged. 5. When protein-depleted rats were similarly given retinal, the rate of reduction of the aldehyde, and the consequent deposition in the liver of retinol and its esters, progressively decreased with reduced protein intake.

Aldehydes↗