HISTOLOGICAL CHANGES IN THE ANTERIOR PITUITARY GLAND OF RATS INTOXICATED WITH BENZENE

1958 ◽  
Vol 17 (4) ◽  
pp. 444-NP ◽  
Author(s):  
A. IANNACCONE ◽  
G. CICCHELLA

SUMMARY Changes occurring in the rat anterior pituitary after daily subcutaneous injections of 0·5 ml. benzene/kg body weight for 22 days have been studied using histochemical methods. The acidophil cells and the 'β' cells exhibit a closer relationship to the blood vessels and a reduction in their cytoplasmic granulation, associated with an increase in the chromidial substance and with enlarged and weakly stained nuclei. The most prominent change discernible in the 'δ' cells is the vesiculation of the cytoplasm, sometimes giving the typical appearance of 'signet-ring' castration cells. These alterations have been interpreted as indicating an increased secretion of simple protein hormones (especially adrenocorticotrophic hormone) and thyrotrophic hormone by the rat pituitary, and a decreased discharge of follicle stimulating and luteinizing hormone.

Author(s):  
E.P. Dolgov ◽  
◽  
A.A. Abramov ◽  
E.V. Kuzminova ◽  
E.V. Rogaleva ◽  
...  

The article presents the data on the study of the influence of mycotoxins combination (T-2 toxin at the concentration of 0.095 mg/kg and aflatoxin B1 in the concentration of 0.019 mg/kg) on the body of quails and the results of pharmacocorrection of toxicosis with a complex consisting of beet pulp and lecithin. Structural changes in the intestines of quais at fodder mycotoxicosis are described. The use of antitoxic feed additives in poultry led to a weakening of the action of xenobiotics, which was confirmed by an increase in the safety of poultry and increase in body weight of quails, a decrease in the clinical manifestations of intoxication, as well as in positive changes in the structure of the intestine of the poultry during histological examination.


1980 ◽  
Vol 87 (1) ◽  
pp. 95-103 ◽  
Author(s):  
G. DELITALA ◽  
T. YEO ◽  
ASHLEY GROSSMAN ◽  
N. R. HATHWAY ◽  
G. M. BESSER

The inhibitory effects of dopamine and various ergot alkaloids on prolactin secretion were studied using continuously perfused columns of dispersed rat anterior pituitary cells. Bromocriptine (5 nmol/l) and lisuride hydrogen maleate (5 nmol/l) both inhibited prolactin secretion, the effects persisting for more than 3 h after the end of the administration of the drugs. A similar although less long-lasting effect was observed with lergotrile (50 nmol/l) and the new ergoline derivative, pergolide (5 nmol/l). These effects contrasted with the rapid disappearance of the action of dopamine. The potency estimates of the ergots relative to that of dopamine were: lergotrile, 2·3; bromocriptine, 13; lisuride, 15; pergolide, 23. The dopamine-receptor blocking drugs, metoclopramide and haloperidol, antagonized the prolactin release-inhibiting activity of the compounds; bromocriptine and lisuride showed the highest resistance to this dopaminergic blockade. The results suggested that the direct effect of the ergot derivatives on dispersed pituitary cells was mediated through dopamine receptors and emphasized the long-lasting action of bromocriptine and lisuride in vitro.


1942 ◽  
Vol 75 (5) ◽  
pp. 547-566 ◽  
Author(s):  
B. A. Houssay ◽  
V. G. Foglia ◽  
F. S. Smyth ◽  
C. T. Rietti ◽  
A. B. Houssay

The ability of the pancreas, from various types of dogs, to correct diabetic hyperglycemia has been studied (Table XI). The pancreas from one animal was united by a vascular union with the neck blood vessels of another dog which had been pancreatectomized for 20 hours. The time necessary to reduce the blood sugar level to 120 mg. per cent was determined. 1. Pancreas from 6 hypophysectomized dogs produced a normal insulin secretion, showing that an anterior pituitary hormone is not necessary for its production or maintenance. 2. In 14 of 17 normal dogs given anterior pituitary extract for 3 or more consecutive days and presenting diabetes (fasting blood sugar 150 mg. per cent or more) the pancreas showed diminished insulin production. 3. In animals which remained diabetic after discontinuing the injections of hypophyseal extract, the pancreas islands were markedly pathologic and the insulin secretion was practically nil. 4. When hyperglycemia existed on the 2nd to 5th day but fell later, the insulin secretion of 5 dogs was normal in 2, supernormal in 1, and less than normal in 2. Histologic examination showed a restoration of beta cells. 5. In 14 dogs resistant to the diabetogenic action of anterior pituitary extract, as shown by little or no change in blood sugar, the pancreatic secretion of insulin was normal in 6 cases, supernormal in 3, and subnormal in 5 cases. Clear signs of hyperfunction of B cells were observed. In 6 resistant animals a high blood sugar (150 mg. per cent) appeared shortly before transplanting, but insulin secretion was normal in 4, supernormal in 1, and subnormal in 1 case. 6. With one injection of extract and 1 day of hyperglycemia the capacity of the pancreas to secrete insulin was not altered. 7. A high blood sugar level lasting 4 days does not alter the islets. The hypophyseal extract acts, therefore, by some other mechanism. In normal dogs, the continuous intravenous infusion of glucose for 4 days maintained the blood sugar at levels as high as those after pituitary extract. In these animals the B cells were hyperplastic and insulin secretion normal. 8. Anterior hypophyseal hyperglycemia is due at first to extrapancreatic factors which are the most important, and last only during the injections of extracts. Pancreatic factors appear afterwards and are responsible for permanent diabetes. Hypophyseal extract produces histological changes in many tissues and damages the Langerhans islands. The coexistent high blood sugar probably exhausts the B cells and exaggerates their injury. 9. In all cases there is a relation between the cytology of the islet B cells and the insulin secreting capacity.


2028 ◽  
Vol 7 (3) ◽  
pp. 253-256
Author(s):  
Atanu FO ◽  
◽  
Momoh S ◽  
Ugwu CE ◽  
Ameh O ◽  
...  

This work investigates the ability of Morinda lucida and co-administration of Morinda lucida/metformin in the control of biochemical and histological changes in alloxan-induced diabetic rats. Alloxan diabetic rats were treated with 200 mg/Kg body weight of Morinda lucida leaves extract, 1 mg/Kg BW of metformin or a combination of the two treatments for 28 days. Results of the studies revealed that Morinda lucida leaves extract significantly improved lipid profile and kidney function in diabetic rats. These positive outcomes were enhanced by combined treated with Morinda lucida leaves extract and metformin. Furthermore, the calculated atherogenic index of treated animals were close to those of normal rats as opposed to diabetic rats. Similarly, histological studies showed that Morinda lucida leaves extract and metformin administered together or singly, ameliorated damages in pancreas and kidneys from alloxan diabetic rats. It can therefore be inferred that combined treatment with Morinda lucida leaves extract and merformin could improve the potency of Morinda lucida leaves used in the management of diabetic complications


2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Ahmed Kaid Naji Allow ◽  
Ayah Rebhi Hilles ◽  
Zainab Yousef ◽  
Norbaiyah Mohamed Bakrim ◽  
Belqees Ahmed ◽  
...  

Introduction: This study evaluates the histological changes of uterine tissue in the female Sprague Dawley rats after administration of Trigonella foenum-graecum (fenugreek) seeds in comparison to combined oral contraceptive pills (COCPs). Methods: Twenty four female Sprague Dawley strain rats of 8 weeks old were divided into A, B, and C groups. Group A was the control and B was administrated with 0.05 mg/kg body weight of COCPs for 15 days. Group C was treated with 750 mg/kg body weight of fenugreek seed aqueous (FSA) extract for 15 days. The uterine tissues were isolated and studied histologically. Results: The uterine weight in the FSA extract treated group was normal, while in the COCPs treated group it was insignificantly increased. The endometrial thickness and endometrial gland density were normal in the FSA extract treated group, while in the COCPs treated group it was atrophied. Decidual-like cells were observed in the COCPs treated group only. Conclusions: Endometrial atrophy and decidual-like cells were noted after COCPs treatment while in the FSA extract and control groups they were absent. The findings suggest that fenugreek seeds could be used as an alternative natural and safe contraceptive product.


1961 ◽  
Vol 23 (2) ◽  
pp. 109-117 ◽  
Author(s):  
K. KOVÁCS

SUMMARY Homotransplantation of the anterior pituitary gland of rats was made into the anterior chamber of the eye. The centre of the grafts developed ischaemic necrosis, but the peripheral zone remained alive to a depth of about 100 μ. During the next 6 weeks there was no evidence of significant regeneration or atrophy of this live peripheral zone, and mitoses were not observed there. The gradual resorption and scarring of the central necrotic area led to a diminution of the overall size of the graft. In the surviving tissue nearly all the chromophil cells became completely degranulated during the first week or two. After 6 weeks only very rare shrunken basophil cells remained, although a few acidophil cells could still be identified. From previous work it is known that such intraocular grafts have very little functional activity. This may possibly be because of the absence of any direct connexion between the graft and the hypothalamus, but the reduction of the total amount of parenchyma may also be an important factor.


1988 ◽  
Vol 254 (4) ◽  
pp. E476-E481 ◽  
Author(s):  
M. Kato ◽  
M. A. Hattori ◽  
M. Suzuki

To further clarify the ionic mechanism of the action of growth hormone (GH)-releasing factor (hGRF) on GH secretion, the involvement of extracellular Na+ was studied in perifused dispersed rat anterior pituitary cells. Replacing extracellular Na+ with mannitol or tris(hydroxymethyl)aminomethane (Tris+) suppressed hGRF- and dibutyryl adenosine 3',5'-cyclic monophosphate (DBcAMP)-induced GH secretion. The peak responses to a 2-min application of 1 nM hGRF were 165.0 +/- 5.6 ng/ml (normal medium, mean +/- SE), 21.2 +/- 1.4 ng/ml (Na+-free, mannitol medium), and 18.0 +/- 1.7 ng/ml (Na+-free, Tris+ medium). GH secretion induced by DBcAMP was also suppressed by Na+ replacement to less than 50% of that in normal medium. However, either 15 or 30 mM KCl-stimulated GH secretion was not markedly affected by replacement of Na+ with either compound. Tetrodotoxin, a voltage-sensitive Na+ channel blocker, had no effect on either hGRF- or excess K+-induced GH secretion. cAMP production by hGRF was not greatly affected by replacing extracellular Na+. Thus extracellular Na+ plays an important role in hGRF-induced GH secretion, especially in the process after cAMP production. The involvement of cAMP-sensitive Na+ channels in hGRF-stimulated GH secretion is discussed.


1956 ◽  
Vol 7 (3) ◽  
pp. 211 ◽  
Author(s):  
KR Norris ◽  
BF Stone

Cattle ticks on four herds in southern Queensland survived dipping in a vat charged with 0.5 per cent. w/v toxaphene, which nevertheless disinfested a fifth herd. Protective periods afforded by toxaphene against attachment of resistant larvae were much shorter than against susceptible strains. Laboratory concentration-response tests on a culture of the toxaphene-resistant ticks indicated that the median lethal concentration of toxaphene for engorged females was 19 times higher than that of a reference strain, and t h at f o r the larvae was also significantly higher. The toxaphene-resistant ticks were not affected when cows were sprayed with 0.05 per cent. w/v gamma-BHC. This was consistent with an earlier history of BHC resistance in the ticks on these herds. Spraying trials indicated no marked arsenic resistance in the toxaphene-resistant ticks. The mortality of the toxaphene-resistant ticks on cattle sprayed with 0.5 per cent. W/V pp'-DDT, and the protective period against larval reinfestation, were as high as usually observed in other tick populations. A very high kill resulted from spraying the toxaphene-resistant ticks with 0.05 per cent. w/v diazinon. Subcutaneous injections of peanut oil solutions of lindane, dieldrin, and aldrin at the rate of 25 mg toxicant/kg host body weight were without effect on toxaphene-resistant ticks.


1982 ◽  
Vol 95 (2) ◽  
pp. 229-235 ◽  
Author(s):  
Susan G. Daniel ◽  
D. B. Ramsden

The release of immunoreactive β-endorphin from rat anterior pituitary cells in culture was studied by radioimmunoassay and gel-filtration chromatography. Two forms of immunoreactivity were detected corresponding to β-lipotrophin (β-LPH) and β-endorphin. Cells were found to release β-endorphin-like immunoreactivity (β-endorphin LIR) into the culture medium for up to 10 days with a trough in release occurring between days 2–4. The ratio of β-LPH to β-endorphin released remained constant during the course of culture. After 4 days in culture β-endorphin LIR release was constant and responsive to modulation. Incubation with lysine-vasopressin (0·1 units/ml) produced a two- to threefold increase in release and dexamethasone (10−6 mol/l) suppressed release to 33% of controls. Neither stimulation nor suppression resulted in a change in the ratio of β-LPH to β-endorphin released. Dexamethasone suppression was not overcome by removal of dexamethasone or addition of vasopressin.


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