UTILIZATION BY THE RAT OF LARGE LIVER RESERVES OR OF A SMALL DAILY INTAKE OF VITAMIN A

1962 ◽  
Vol 40 (1) ◽  
pp. 1407-1413
Author(s):  
T. K. Murray

Weanling female rats were given a massive dose of vitamin A and thereafter fed a vitamin A free diet while similar rats were provided with the same diet plus a small daily intake of vitamin A for the entire period. Some of the rats from each group were bred to normal males. There were no differences in the growth rate, the number of young produced and weaned, nor in the weight of the young. Somewhat more vitamin A was transferred to the liver and kidney of the young by mothers with large liver stores but these differences had disappeared by weaning age. It was concluded that sufficient vitamin A could be given a rat at weaning to allow normal development and the production of at least one normal litter.

1962 ◽  
Vol 40 (10) ◽  
pp. 1407-1413
Author(s):  
T. K. Murray

Weanling female rats were given a massive dose of vitamin A and thereafter fed a vitamin A free diet while similar rats were provided with the same diet plus a small daily intake of vitamin A for the entire period. Some of the rats from each group were bred to normal males. There were no differences in the growth rate, the number of young produced and weaned, nor in the weight of the young. Somewhat more vitamin A was transferred to the liver and kidney of the young by mothers with large liver stores but these differences had disappeared by weaning age. It was concluded that sufficient vitamin A could be given a rat at weaning to allow normal development and the production of at least one normal litter.


Retinoic acid (vitamin A acid), the carboxylic acid corresponding to the primary alcohol retinol (vitamin A), has previously been thought to fulfil all the functions of vitamin A except in vision, since rats fed a diet deficient in retinol but supplemented with retinoic acid grow well, outwardly appearing healthy, yet become blind. This paper reports that female rats on such a diet had normal oestrous cycles and became pregnant when mated, but always resorbed the foetuses and no litters were born. The first abnormalities detected were necrosis and slight polymorph infiltration around the periphery of the placental disk about the sixteenth day of pregnancy. Supplementation with retinol as late as the tenth day resulted in the birth of a healthy litter. Retinoic acid therefore maintained the early but not the later stages of gestation. When very small amounts of retinol were given during pregnancy, dead or weak young were born; on higher supplements of the vitamin, litters were weaned successfully. By this means young rats were produced with negligible stores of retinol. Male rats fed retinoic acid but not retinol had small and often oedematous testes. The germinal epithelium sloughed off and in some tubules the lumen was obliterated, but in others the lumen remained, and in these some spermatocytes and spermatogonia were held tenaciously. The seminal vesicles were smaller than in controls given retinol. In rats born with negligible stores of retinol—see above—and maintained on retinoic acid, the testes remained infantile; spermatids were never formed. Feeding retinol restored spermatogenesis in degenerate testes and promoted the normal development of testes that had remained infantile; it also ensured the growth of the seminal vesicles. Retinoic acid did not therefore serve in reproduction, although it replaced the true vitamin in maintaining life, growth and general health. Besides the latter so-called systemic function, vitamin A must have a discrete and specific role in reproduction, viz. that performed by retinol but not by retinoic acid. From among the many previously reported features of disordered reproduction in vitamin A-deficient animals, it was possible to distinguish which had arisen from a failure of this specifically ‘reproductive’ role and which from a ‘systemic’ deficiency. The inactivity of retinoic acid in reproduction demonstrates that in rats vitamin A has not two, as previously thought, but three dissociable modes of action: (1) systemic; (2) in vision; and (3) in reproduction.


1969 ◽  
Vol 111 (1) ◽  
pp. 97-105 ◽  
Author(s):  
H. S. Juneja ◽  
N. R. Moudgal ◽  
J. Ganguly

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-17β, 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 Δ5-3β-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.


1965 ◽  
Vol 43 (10) ◽  
pp. 1625-1632 ◽  
Author(s):  
Sheila I. Read ◽  
W. P. McKinley

Rats of different ages were fed a diet containing 10 p.p.m. parathion with or without vitamin A supplementation for various periods of time, and the effects on liver and kidney carboxylesterases were measured.Marked inhibition of carboxylesterases was observed shortly after the parathion diet was introduced. The degree of inhibition was not altered appreciably by continued feeding of the diet containing parathion. Young female rats showed some recovery of liver carboxylesterases on continued feeding of the parathion diet. After removal of vitamin A from the diet, the levels of liver carboxylesterases of male rats fed parathion increased appreciably.


1965 ◽  
Vol 43 (3) ◽  
pp. 317-322 ◽  
Author(s):  
Sheila I. Read ◽  
T. K. Murray ◽  
W. P. McKinley

DDT (100 p.p.m.) was added to the diet of female rats that were then bred to males receiving the same diet. Liver carboxylesterase and liver and kidney vitamin A levels were measured in the dams and their young at parturition and at weaning.DDT did not have any adverse effect on the breeding performance of the adults or on the vitamin A stores of the newborn or weanling rats. Vitamin A stores of the dams were reduced by the pesticide. Liver carboxylesterase increased greatly between birth and weaning and remained almost constant thereafter. DDT caused a marked increase in liver carboxylesterase over and above that which occurred during growth.


1968 ◽  
Vol 58 (4) ◽  
pp. 600-612 ◽  
Author(s):  
Robert Boyd ◽  
Donald C. Johnson

ABSTRACT The effects of various doses of testosterone propionate (TP) upon the release of luteinizing hormone (LH or ICSH) from the hypophysis of a gonadectomized male or female rat were compared. Prostate weight in hypophysectomized male parabiotic partners was used to evaluate the quantity of circulating LH. Hypophyseal LH was measured by the ovarian ascorbic acid depletion method. Males castrated when 45 days old secreted significantly more LH and had three times the amount of pituitary LH as ovariectomized females. Administration of 25 μg TP daily reduced the amount of LH in the plasma, and increased the amount in the pituitary gland, in both sexes. Treatment with 50 μg caused a further reduction in plasma LH in males, but not in females, while pituitary levels in both were equal to that of their respective controls. LH fell to the same low level in partners of males or females receiving 100 μg TP. When gonadectomized at 39 days, males and females had the same amount of plasma LH, but males had more stored hormone. Pituitary levels were unchanged from controls following treatment with 12.5, 25 or 50 μg TP daily, but plasma values dropped an equal amount in both sexes with the latter two doses. Androgenized males or females, gonadectomized when 39 days old, were very sensitive to the effects of TP and plasma LH was significantly reduced with 12.5 μg daily. Pituitary LH in androgenized males was higher than that of normal males but was reduced to normal by small amounts of TP. The amount of stored LH in androgenized females was not different from that of normal females and it was unchanged by any dose of TP tested. Results are consistent with the conclusion that the male hypothalamic-hypophyseal axis is at least as sensitive as the female axis to the negative feedback effects of TP. Androgenization increases the sensitivity to TP in both males and females.


Toxins ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 537
Author(s):  
Tarana Arman ◽  
John D. Clarke

Microcystins are ubiquitous toxins produced by photoautotrophic cyanobacteria. Human exposures to microcystins occur through the consumption of contaminated drinking water, fish and shellfish, vegetables, and algal dietary supplements and through recreational activities. Microcystin-leucine-arginine (MCLR) is the prototypical microcystin because it is reported to be the most common and toxic variant and is the only microcystin with an established tolerable daily intake of 0.04 µg/kg. Microcystin toxicokinetics is characterized by low intestinal absorption, rapid and specific distribution to the liver, moderate metabolism to glutathione and cysteinyl conjugates, and low urinary and fecal excretion. Molecular toxicology involves covalent binding to and inhibition of protein phosphatases, oxidative stress, cell death (autophagy, apoptosis, necrosis), and cytoskeleton disruption. These molecular and cellular effects are interconnected and are commonly observed together. The main target organs for microcystin toxicity are the intestine, liver, and kidney. Preclinical data indicate microcystins may also have nervous, pulmonary, cardiac, and reproductive system toxicities. Recent evidence suggests that exposure to other hepatotoxic insults could potentiate microcystin toxicity and increase the risk for chronic diseases. This review summarizes the current knowledge for microcystin toxicokinetics, molecular toxicology, and pathophysiology in preclinical rodent models and humans. More research is needed to better understand human toxicokinetics and how multifactorial exposures contribute to disease pathogenesis and progression.


2019 ◽  
Vol 122 (11) ◽  
pp. 1295-1302 ◽  
Author(s):  
Takehiro Michikawa ◽  
Shin Yamazaki ◽  
Makiko Sekiyama ◽  
Tatsuo Kuroda ◽  
Shoji F. Nakayama ◽  
...  

AbstractThe pathogenesis of congenital diaphragmatic hernia (CDH) is largely unknown; however, vitamin A seems to play a role in diaphragmatic development. Previous case–control studies reported that maternal dietary vitamin A intake was inversely associated with the risk of CDH. To our knowledge, however, there is no prospective evidence regarding this association. Our aim was to examine whether maternal intake of vitamin A was associated with CDH occurrence. Baseline data, from the Japan nationwide birth cohort study (2011–2014) of 89 658 mothers (mean age at delivery = 31·2 years) who delivered singleton live births, were analysed. We assessed dietary habits using an FFQ focused on the first trimester and estimated the daily intake of total vitamin A (retinol activity equivalents), retinol, provitamin A carotenoids and vegetables. The occurrence of CDH was ascertained from medical records. A total of forty cases of CDH were documented. The adjusted OR of CDH occurrence for the high total vitamin A intake category (median = 468 μg/d) was 0·6 (95 % CI 0·3, 1·2) with reference to the low intake category (230 μg/d). When we restricted to mothers with a prepregnancy BMI of 18·5–24·9 kg/m2, vitamin A intake was inversely associated with the risk of their children being born with CDH (OR 0·5, 95 % CI 0·2, 1·0). Even given the limited number of cases in the study, our findings provide additional evidence to link vitamin A with CDH.


2012 ◽  
Vol 63 (4) ◽  
pp. 417-427 ◽  
Author(s):  
Mariana Tozlovanu ◽  
Delphine Canadas ◽  
Annie Pfohl-Leszkowicz ◽  
Christine Frenette ◽  
Robert J. Paugh ◽  
...  

AbstractIn the present study the photoreactivity of the fungal carcinogen ochratoxin A (OTA) has been utilised to generate authentic samples of reduced glutathione (GSH) and N-acetylcysteine (NAC) conjugates of the parent toxin. These conjugates, along with the nontoxic OTα, which is generated through hydrolysis of the amide bond of OTA by carboxypeptidase A, were utilised as biomarkers to study the metabolism of OTA in the liver and kidney of male and female Dark Agouti rats. Male rats are more susceptible than female rats to OTA carcinogenesis with the kidney being the target organ. Our studies show that the distribution of OTA in male and female rat kidney is not significantly different. However, the extent of OTA metabolism was greater in male than female rats. Much higher levels of OTα were detected in the liver compared to the kidney, and formation of OTα is a detoxification pathway for OTA. These findings suggest that differences in metabolism between male and female rats could provide an explanation for the higher sensitivity of male rats to OTA toxicity


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