Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 3
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

Lipogranulomas are lesions found in histopathological liver examination in humans and in various animal species, including dogs, especially those with portosystemic shunts. They consist of macrophages and other inflammatory cells, and sometimes they contain iron salts (pigment granuloma). This study aimed at determining the number of granulomas and cellular composition of lipogranulomas in dogs with the congenital extrahepatic portosystemic shunt, and to identify factors associated with their development. 44 archival liver samples from dogs with portosystemic shunt were stained using HE, Perl’s method and – in randomly-selected cases – immunohistochemically against CD56, CD20 and CD3 (DAKO). A reduction in the size of the liver was observed in all dogs during laparotomy, and the diameter of the vessel circumventing the liver was also measured (in 24 dogs). Lipogranulomas were found in 52.3% of samples; iron salts were present in 47.8% of them; 72% of cells in lipogranulomas were macrophages. In lipogranulomas both types of lymphocytes – T and B – were seen. The presence of lipogranulomas in liver samples in dogs was connected with fatty degeneration of hepatocytes and was correlated with the age of animals and with the diameter of the abnormal vessel circumventing the liver. Their formation appears to be triggered by severe ischemia and shortage of nutrient supply.
Go to article

Authors and Affiliations

M. Sobczak-Filipiak
T. Męcik-Kronenberg
M. Czopowicz
M. Galanty
P. Trębacz
J. Frymus
I. Badurek
J. Szarek
Download PDF Download RIS Download Bibtex

Abstract

The aim of the study was to compare the effects of corneal healing in case of application of stem cells in various forms, in relation to the antibiotic-assisted procedures. Rabbits were divided into 4 groups in the first stage of the experiment. Group 0 (negative control group) was not subjected to any actions, which would cause damage to the cornea. The remaining three groups had their cornea damaged. Group 1 (positive control group) – no drugs were administered during the experiment. Rabbits in group 2 were administered with ointment containing stem cells to the lesion, while group 3 – with ofloxacinum. The stem cells were administered during the first five days, twice a day, onto the corneal surface. The further course of the experiment consisted of observing the rate of healing of the injured cornea and assessment of its transparency, size of lesion, hyperaemia, eyelid spasm and outflow from the conjunctival sac after 5, 10 and 20 days.

In the second stage the animals were euthanised after clinical examination on the twentieth day of the experiment, in order to analyse the corneal reparative processes on the same day. The studies revealed that the application of antlerogenic stem cells had a positive effect on the healing process of corneal defects. The application thereof not only shortened the healing time, but also weakened or arrested the development of side effects. The results have demonstrated that the epithelial proliferation in each group was different. The longest was maintained in the group with stem cells, the shortest – in the group with chemotherapeutics. The use of antlerogenic stem cells had a positive effect on the healing process of corneal lesions. The use of stem cells helped to maintain high transparency of the cornea.

Go to article

Authors and Affiliations

M. Kiełbowicz
P. Kuropka
M. Cegielski
Z. Kiełbowicz
P. Trębacz
M. Hebel
R. Aleksiewicz
Download PDF Download RIS Download Bibtex

Abstract

In 46 dogs with congenital portosystemic shunt (cPSS) histopathological examination of the pancreas, including measuring of the islet area, was performed, and the results were compared with those obtained in 6 control dogs without cPSS. Pancreatic islets were found in 43 (94%) dogs with cPSS and in all control animals. Mean area of the pancreatic islets was significantly lower in cPSS patients (median of 2219.4 μm2, interquartile range [IQR] from 1559.0 to 3146.2 μm2, range from 485.4 to 10333.4 μm2) than in control dogs (median of 8705.5 μm2, IQR from 8284.4 to 9329.2 μm2, range from 7689.9 to 9624.2 μm2) (p<0.001). The area of pancreatic islets was weakly, but significantly, positively correlated with the body weight of dogs (r=0.32, p=0.026), but not with the age or sex. Vacuoles were found in the cytoplasm of pancreatic islet cells in 37 (87%) dogs with cPSS and in none of the control animals (p<0.001). Their presence was not linked to the sex, breed, age or body weight. Extracellular homogenous eosinophilic masses were present in pancreatic islets in 5 (12%) cPSS patients and in none of control animals. Connective tissue hyperplasia was found in pancreatic islets of 4 (9%) dogs with cPSS and in none of the control dogs. These results indicate that cPSS severely affects the pancreas, as shown by significantly reduced area of the islets, and the presence of eosinophilic masses in the pancreas and/or intracellular vacuoles.
Go to article

Bibliography


Baade S, Aupperle H, Grevel V, Schoon HA (2006) Histopathological and immunohistochemical investigations of hepatic lesions associated with congenital portosystemic shunt in dogs. J Comp Pathol 134: 80-90.

Collings AJ, Gow AG, Marques A, Yool D, Furneaux R, Mellanby R, Watson PJ (2012) A prospective study of basal insulin concentrations in dogs with congenital portosystemic shunts. J Small Anim Pract 53: 228-233.

Cui W, Cui H, Peng X, Fang J, Zuo Z, Liu X, Wu B (2011) Changes of relative weight and cell cycle, and lesions of bursa of Fabricius in-duced by dietary excess vanadium in broilers. Biol Trace Elem Res 143: 251-260.

Frymus J, Trębacz P, Degórska B, Sterna J, Kowalczyk P, Tomkowicz A, Galanty M (2015) Portosystemic shunt in dogs and cats. Current diagnostic aspects. Magazyn Wet 24: 12-22

Frymus J, Trębacz P, Sobczak-Filipiak M, Czopowicz M, Degórska B, Galanty M (2020) Histopathological picture of pancreatic islets in dogs with congenital portosystemic shunt. Med Weter 76: 103-106.

Gow AG (2017) Hepatic encephalopathy. Vet Clin North Am Small Anim Pract 47: 585-599.

Kikumoto Y, Sugiyama H, Inoue T, Morinaga H, Takiue K, Kitagawa M, Fukuoka N, Saeki M, Maeshima Y, Wang DH, Ogino K, Masuoka N, Makino H (2010) Sensitization to alloxan-induced diabetes and pancreatic cell apoptosis in acatalasemic mice. Biochim Biophys Acta 1802: 240-246.

Kraun MB, Nelson LL, Hauptman JG, Nelson NC (2014) Analysis of the relationship of extrahepatic portosystemic shunt morphology with clinical variables in dogs: 53 cases (2009-2012). J Am Vet Med Assoc 245: 540-549.

Majd N E, Tabandeh MR, Shahriari A, Soleimani Z (2018) Okra (Abelmoscus esculentus) improved islets structure, and down-regulated PPARs gene expression in pancreas of high-fat diet and streptozotocin-induced diabetic rats. Cell J 20: 31-40.

Mankin KM (2015) Current concepts in congenital portosystemic shunts. Vet Clin North Am Small Anim Pract 45: 477-487.

Masjedi F, Gol A, Dabiri S (2013) Preventive effect of garlic (Allium sativum L.) on serum biochemical factors and histopathology of pan-creas and liver in streptozotocin-induced diabetic rats. Iran J Pharm Res 12: 325-338.

Morandi F, Sura PA, Sharp D, Daniel GB (2010) Characterization of multiple acquired portosystemic shunts using transplenic portal scintig-raphy. Vet Radiol Ultrasound 51: 466-471.

Muranishi T, Takehana K, Hiratsuka T, Kobayashi A, Eerdunchaolu, Iwasa K, Abe M (1999) An investigation of the relationship between duct system and A cell-rich and PP cell-rich pancreatic islets in the canine pancreas. J Vet Med Sci 61: 737-742.

Noda K, Melhorn MI, Zandi S, Frimmel S, Tayyari F, Hisatomi T, Almulki L, Pronczuk A, Hayes KC, Hafezi-Moghadam A (2010) An animal model of spontaneous metabolic syndrome: Nile grass rat. FASEB J 24: 2443-2453.

Perazzo JC, Tallis S, Delfante A, Souto PA, Lemberg A, Eizayaga FX, Romay S (2012) Hepatic encephalopathy: an approach to its multiple pathophysiological features. World J Hepathol 4: 50–65.

Przybylik-Mazurek E, Pach D, Hubalewska-Dydejczyk A, Sowa-Staszczak A, Gilis-Januszewska A, Kulig J, Matyja A, Chrapczyński P (2012) Symptoms and early diagnostic possibilities of pancreatic endocrine cells hyperplasia (nesidioblastosis). Przegląd Lekarski 69: 9-14.

Raffel A, Krausch MM, Anlauf M, Wieben D, Braunstein S, Klöppel G, Röher HD, Knoefel WT (2007) Diffuse nesidioblastosis as a cause of hyperinsulinemic, hypoglycemia in adults: a diagnostic and therapeutic challenge. Surgery 141: 179-184.

Sobczak-Filipiak M, Szarek J, Czopowicz M, Galanty M, Dolka I, Trębacz P, Frymus J, Lechowski R (2018a) Stellate cells in livers of dogs with portal vein hypoperfusion. Med Weter 74: 392–397

Sobczak-Filipiak M, Męcik-Kronenberg T, Czopowicz M, Galanty M, Trębacz P, Frymus J, Badurek I, Szarek J (2018b) Lipogranulomas and pigment granulomas in livers of dogs with portosystemic shunt. Pol J Vet Sci 21: 265-272.

Sobczak-Filipiak M, Szarek J, Badurek I, Padmanabhan J, Trębacz P, Januchta-Kurmin M, Galanty M (2019) Retrospective Liver Histomor-phological Analysis in Dogs in Instances of Clinical Suspicion of Congenital Portosystemic Shunt. J Vet Res;63: 243-249.

Tivers MS, Handel I, Gow AG, Lipscomb VJ, Jalan R, Mellanby RJ (2014) Hyperammonemia and systemic inflammatory response syn-drome predicts presence of hepatic encephalopathy in dogs with congenital portosystemic shunts. PLoS One 9: e82303.

Tobias KM, Rohrbach BW (2003) Association of breed with the diagnosis of congenital portosystemic shunts in dogs: 2,400 cases (1980-2002). J Am Vet Med Assoc 223: 1636-1639.

Yabe K, Yamamoto Y, Suzuki T, Takada S, Mori K (2019) Functional and morphological characteristics of pancreatic islet lesions induced by quinolone antimicrobial agent gatifloxacin in rats. Toxicol Pathol 47: 35-43.

Zhang B, Li SS, Men JL, Zhang ZH (2018) Effect of long-term crotonaldehyde exposure on heart damage in male rats. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 36: 647-652
Go to article

Authors and Affiliations

J. Frymus
1
P. Trębacz
1
M. Sobczak-Filipiak
2
M. Czopowicz
3
M. Galanty
1

  1. Department of Small Animal Diseases with Clinic, Warsaw University of Life Sciences – SGGW, Nowoursynowska 159c, 02-776 Warszawa, Poland
  2. Department of Pathology and Veterinary Diagnostics, Warsaw University of Life Sciences – SGGW, Nowoursynowska 159c, 02-776 Warszawa, Poland
  3. Division of Veterinary Epidemiology and Economics, Institute of Veterinary Medicine, Warsaw University of Life Sciences – SGGW, Nowoursynowska 159c, 02-776 Warszawa, Poland

This page uses 'cookies'. Learn more