Printer Friendly

The structural changes of the rat's lung induced by intraperitoneal injection of 5-fluorouracil.

Byline: Muna Zuhair Al-Hamdany and Abduljabbar Yasin Muhammed Al-Hubaity

AbstractObjective: To record the main structural changes in the rat's lung induced by administration of 5-fluorouracil.Methods: The case-control study was conducted at College of Medicine, Mosul, Iraq, from December 2012 to June2013. Two groups of 6 rats each were used. The experimental group was given 20mg of 5-fluorouracil in 2ml normal saline per kg body weight by intraperitoneal injection for 7 consecutive days, while the other group was given 2ml normal saline per kg body weight intraperitoneally for 7 days and served as the control group. Specimens of lung tissue of the two groups were taken and prepared for light microscopic examination.Result: Structural changes were found in the experimental (5-fluorouracil) group compared to the controls, including abnormal alveolar duct, sac, and terminal bronchioles with emphysematous changes in most of the alveoli in addition to peribronchiolitis, perivasculitis, inflammatory cells infiltration and interstitial fibrosis.Conclusion: 5-fluorouracil has toxic effects on the lung tissue resulting in emphysema and interstitial fibrosis.Keywords: 5-fluorouracil, Rat, Lung, Emphesema, Interstitial fibrosis

IntroductionChemotherapy involves the use of chemical agents to combat the neoplastic growth which affects some tissues and organs, but it does not distinguish between the neoplastic and normal cells as it eliminates the fast- growing cancer cells and other healthy cells in the body, including those lining digestive and respiratory tracts.1

A potent antimetabolite is 5-fluorouracil (5-FU) that acts during the S phase of the cell cycle. It is activated by thymidine phosphrylase enzyme into fluorodeoxyuridylate (5-fluoro-2'deoxyuridine-5'monophosphate, or 5-FdUMP) which inhibits thymidylate synthase, thus preventing deoxyribonucleic acid (DNA) synthesis.2 The concentration of thymidine phosphorylase is 3-10 folds higher in tumour cells compared to its concentration in the healthy tissues, and this can enable selective drug activation of 5-FU at the tumour site with limitation of systemic toxicity.3

The 5-FU is metabolised through the liver and has a half- life of about 10 minutes.4 The common clinical side effects of 5-FU include myelosuppression, diarrhoea, vomiting and mucositis. However, in the last decade, cardiotoxicity and neurotoxicity have also been reported.5

The trade names of 5-FU are Efudex, Carac, Fluroplex, and it is widely used alone or as a combined protocol in the treatment of various malignancies, includinggastrointestinal, breast, head and neck, basal cell carcinoma of skin (as a cream) and in ophthalmic surgery.6

Since there are no literature available concerning the effects of 5-FU on the respiratory system, particularly on the lungs, the present study was, therefore, carried out to record any changes in the structure of the lungs during its use in the treatment of some malignancies.

Material and MethodsThe case-control study was conducted at the animal house of the College of Medicine, University of Mosul, Iraq from December 2012 to June 2013 as part of a Ph.D thesis, and comprised 12 healthy adult female Wistar albino rats of about 3 months age and 200-250gm weight. The animals were kept at room temperature of about 25C and all animals were allowed free access to laboratory pellet foods and tap water drink.

The animals were randomly distributed into 2 equal groups. In Group I, each animal was given 2ml/kg body weight/day of normal saline by intraperitoneal injection for 7consecutive days. This served as the control group.

In Group II, each animal was given 5-FU 20mg in 2ml normal saline (as a carrier solution) per kg body weight per day by intraperitoneal injection once daily for 7 consecutive days. This served as the experimental group.

One day after the last injection of the two groups, all the animals were dissected under light ether to extract the two lungs from each animal. The extracted lungs were then fixed in 10% neutral buffered formalin solution for about 48 hours. Small pieces of about 2-3mm in size were obtained from each lung and paraffin blocks were prepared for light microscopic examination. All sections were processed according to Luna7 and Dury's methods.8

Serial sections of about 5 microns in thickness were collected from each paraffin block using Reichert's Rotatory Microtome. The tissue sections were stained with Harris Haematoxylin and Eosin (HandE) stain and Masson's Trichrome stain. All the stained sections were examined using Compound PhotoMicroscope and some micrographs were taken from some sections using BEl Photonice microscope.

ResultsIn the control group, normal alveolar duct, alveolar spaces and terminal bronchioles with regular size and shape of the alveoli were found (Figure-1). Besides, thin interalveolar septae between the adjacent alveoli was lined by spindle shaped pneumocytes type I and rounded shaped pneumocytes type II (Figure-2). Few collagen fibers in the wall of alveolar spaces, in the wall of pulmonary capillary and in the wall of terminal bronchiole was seen on using Masson's Trichrome stain (Figure-3).

Among the cases, abnormal terminal bronchioles and pulmonary vessels showing features of peribronchiolitis and perivasculitis appeared as thickening in the wall of terminal bronchiole and in the wall of pulmonary vessels due to lymphocytic infiltration (Figure-4). There was congestion within the pulmonary vessels with adipocytic infiltration within the pulmonary lobule (Figure-5).

Also seen were abnormal alveolar spaces with rupture and fusion of some adjacent alveoli causing emphysematous dilatation (Figure-5 and 6) with hyperplasia of bronchus associated lymphatic tissue(BALT), forming lymphoid follicles or aggregates.

Besides, there was thickening of interalveolar septae with haemorrhage and congestion of the capillary bed and mononuclear inflammatory cells infiltration both within and in the wall of alveoli (Figure-7). Interstitial fibrosis and accumulation of collagen fibres in between the alveoli with congestion and fibrosis of capillary bed causing thickening of interalveolar septae was also present (Figure-8).Congestion and fibrosis around the pulmonary vessels with blood clot formation and mononuclear cell infiltration in the perivascular area was also seen (Figure-9). And, finally, there were increased collagen fibres due to hyperproliferation of fibroblasts in addition to mononuclear cell infiltration around the terminal bronchioles (Figure-10).

DiscussionThe drug 5-FU is usually given with a carrier in case of intraperitoneal injection. The best carrier which can be used in case of gastrointestinal tumours is HAS-Steri solution (neotype 6% hydroxyethyl starch), as this carrier will delay the absorption of 5-FU from the peritoneal cavity. This exposes the metastatic cells in the peritoneal cavity to 5-FU for a longer time before being absorbed by the peritoneum.9 Despite this fact we used the normal saline solution as a carrier for 5-FU as we wanted to get quicker absorption from the peritoneum and to achieve a higher level of toxicity of the drug as we were dealing with experimental model study, and not with the treatment of malignancies.

The occurrence of various structural changes in the lung tissue induced by 5-FU in our study as emphysema, inflammatory cell infiltration and interstitial fibrosis were nearly similar to what has been reported on the effects of rifampicin and isoniazide on the lung tissue.10,11 There are two types of alveolar cells, type I and type II pneumocytes. The latter produces surfactant whose main function is to lower the surface tension and also to protect the lung from different pathogens.12 It seems that probably 5-FU impaired the alveolar surface tension due to the inadequate production of surfactant caused by the cellular damage of pneumocytes type II induced by the drug and thus most of the alveoli ruptured and communicated with the neighbouring alveoli, leading to emphysema. To the best of our knowledge, no previous explanation for the occurrence of emphysema induced by some drugs has been given by any study.

The major amount of connective tissue has a peribronchial location along with severe inflammatory cell infiltration around the terminal bronchioles (Figure-8) of the current study were nearly similar to what has been noted in the experimental lung fibrosis induced by bleomycin.13,14 This finding could be attributed to degradation induced by the drug, which, in turn, initiated inflammation with inflammatory cell infiltration.

One of the main causes in the pathophysiology and pathogenesis of broncho-pulmonary dysplasia and lung fibrosis is reactive oxidative species (ROS).15,16 It is well known that fibroblasts are responsible for synthesis and secretion of extracellular protein and collagen fibres.17,18In our opinion hyperactivity of fibroblasts induced by 5-FU will lead to accumulation of collagen fibres and extracellular matrix in the interstitial spaces which will be converted into fibrous tissue later on.

Some previous studies noted that in normal lung, pneumocytes type II have been shown to secrete prostaglandin E2, which can act to suppress fibroblast activity and growth.19,20 Thus, in cases of exposure to 5- FU, prostaglandin E2 secretion is reduced, which, in turn,leads to overproduction of fibroblasts and interstitial fibrosis. In addition, the fibroproliferative process may be the potential target for the treatment of pulmonary fibrosis in the future.21

ConclusionThe use of 5 FU in the treatment of some tumours has toxic effect on the structure of the lung, causing emphysema and lung fibrosis probably due to alteration in the surfactant production and reduction in the secretion of prostaglandin E2 and resulting in overproduction of fibroblasts.

References1. El-Sayyad HI, Ismail MF, Shalaby FM, Abou-El-Magd RF, Gaur RL, Fernando A, et al. Histopathological effects of Cisplatin, Doxorubicin and 5-Fluorouracil (5-FU) on the liver ofmale albino rats. Int J Biol Science 2009; 5: 466-73.2. Lemaire L, MaletMartino MC, Forni MD, Martino R, Lasserre B.Cardiotoxicity of commercial 5-fluorouracil vials stems from the alkaline hydrolysis of this drug. Br J Cancer 2000; 66: 119-27.3. Robben NC, Pippas AW, Moore JO. The syndrome of 5-fluorouracil cardiotoxicity: An elusive cardiopathy. Cancer 1993; 71: 493-509.4. Saif MW, Black G, Roy S, Bell D, Russo S, Eloubeidi MA, et al. Phase II study of Capecitabine with concomitant radiotherapy for patients with locallyadvanced pancreatic cancer: up-regulation of thymidine phosphorylase. Cancer J 2007; 13: 247-56.5. Shoemaker LK, Arora U, Lima CM. 5-Fluorouracil-induced coronary vasospasm. Cancer Control 2004; 1: 46-9.6. Sobrero AF, Aschele C, Bertino JR. Fluorouracil in colorectal cancer--a tale of two drugs: implications for biochemical modulation. J Clin Oncol 2000; 15: 368-81.7. Luna LG. Manual of histological staining methods of the armed forces. 3rd ed. New York: McGraw-Hill book Company; 1968. 8. Durary RAB, Wallgton EA, Cameron SR. Carlton's histological techniques, 4th edition. New York: Oxford University Press; 1985.9. Wei ZG, Li Gx, Huang XC, Deng HJ, Qing SH. Pharmacokinetics and tissue distribution of intraperitoneal 5- fluorouracil with a novel carrier solution in rats. World J Gastroenterol 2008; 14: 2179-86.10. Ahmed DH. The effect of Rifampicin and Isiniazid on liver and lung tissues in rats. Iraqi J Pharmacol 2011; 11: 34-45.11. McCoenin MD, Zachary JF. Pathological basic veterinary disease.4th ed. Mosby: Elsevier Inc, 2007; pp 495-6.12. Orgeig S, Hiemstra E, Valdhuizen A. Recent advances in alveolar biology evolution and function of alveolar proteins. Respir Physiol Neurobiol 2010; 173 Suppl: S43-54.13. Grande NR, Peao MND, de Sa CM, Aguas AP. Lung fibrosis induced by bleomycin: structural changes and overview of recent advances. Scanning Microscopy 1998; 3: 487-94.14. Hay I, Shahzeid S, Laurent G. Mechanisms of Bleomycin - induced lung damage. Arch Toxicol 1997; 65: 81-94.15. Danic C, Cecchi A, Bertini G. Role of oxidative stress as physiopathologic factor in the preterm infants. Mine Pediatric2004; 36: 381-94.16. Bandari A, Badari V. Bronchopulmonary dysplasia: an Update.Indian J Pediatrics 2007; 74: 73-7.17. Cein J, Kinsella P. Pathogenesis and treatment of bronchopulmonary dysplasia. Curr Opin Pediatr 2011; 23: 305-13.18. Hayes JR, Meadows JT, Murphy BS, Feola DJ, Shock LA, Ballard HO.Pulmonary function outcomes in bronchopulmonary dysplasia through childhood and into adulthood implications for primary care. Prim Care Respir J 2011; 20: 128-38.19. Nenan S, Boichot E, Lagente V, Bertrand CP. Macrophage elastase(MMP-12): a pro-inflammatory mediator? Mem Inst Oswaldo Cruz2005; 100: 167-72.20. Yao HW, Zhu JP, Zhao MH, Lu Y. Losartan attenuates bleomycin- induced pulmonary fibrosis in rats. Respiration 2006; 73: 236.21. Safaeian L, Jafarian A, Rabbani M, Mirmohammad H, Torabinia N, Alavi S. The effect of AT1 receptor blockade on Bax and Bel-2 expression in Bleomycin- induced pulmonary fibrosis. DARU 2009;17: 53-9.
COPYRIGHT 2014 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2014 Gale, Cengage Learning. All rights reserved.

 
Article Details
Printer friendly Cite/link Email Feedback
Publication:Journal of Pakistan Medical Association
Date:Jul 31, 2014
Words:2009
Previous Article:Changes in brain metabolites in experimental cerebral malaria infection with plasmodium berghei ANKA: A literature review.
Next Article:The value of serum NGAL in determination of dialysis indication.
Topics:

Terms of use | Privacy policy | Copyright © 2018 Farlex, Inc. | Feedback | For webmasters