Int J Stem Cells.  2015 Nov;8(2):170-180. 10.15283/ijsc.2015.8.2.170.

Therapeutic Effect of Adipose Derived Stem Cells versus Atorvastatin on Amiodarone Induced Lung Injury in Male Rat

Affiliations
  • 1Department of Histology, Faculty of Medicine, Cairo University, Cairo, Egypt. maha_kaah@yahoo.com
  • 2Department of Clinical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.
  • 3Department of Plastic Surgery, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.

Abstract

BACKGROUND AND OBJECTIVES
Amiodarone (AM), a class 3 antiarrhythmic drug, has been associated with variety of adverse effects, the most serious of which is pulmonary toxicity. Ator (A) is a statin, known for their immunomodulatory and anti-inflammatory activities. Recent studies provide evidence of potential therapeutic effect of statins on lung injury. Adipose derived stem cells (ADSCs) have shown great promise in the repair of various tissues. The present study aimed at investigating and comparing the possible therapeutic effect of A and ADSCs on AM induced lung injury in albino rats.
METHODS AND RESULTS
34 adult male albino rats were divided into 5 groups: control group (Gp I), A group (Gp II) received 10 mg/kg of A orally 6 days (d)/week (w) for 4 weeks (ws), AM group (Gp III) received 30 mg/kg of AM orally 6 d/w for 4 ws, AM&A group (Gp IV) received AM for 4ws then A for other 4 ws and AM&SCs group (Gp V) received AM for 4 ws then injected with 0.5 ml ADSCs on 2 successive days intravenously (IV). Histological, histochemical, immunohistochemical and morphometric studies were performed. Group III displayed bronchiolitis obliterans, thickened interalveolar septa (IAS) and thickened vascular wall which were proven morphometrically. Increased area% of collagen fibers and apoptotic changes were recorded. All findings regressed on A administration and ADSCs therapy.
CONCLUSION
Ator proved a definite ameliorating effect on the degenerative, inflammatory, apoptotic and fibrotic changes induced by AM. ADSCs administration denoted more remarkable therapeutic effect compared to A.

Keyword

Lung; Amiodarone; Ator; ADSCs

MeSH Terms

Adult
Amiodarone*
Animals
Atorvastatin Calcium
Bronchiolitis Obliterans
Collagen
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Lung Injury*
Lung*
Male*
Rats*
Stem Cells*
Amiodarone
Collagen

Figure

  • Fig. 1 Lung sections of control rats (H&E) showing (A): a bronchiole (B), a venule (V), an arteriole (ar), alveoli (a), alveolar sacs (A) and IAS (I) (×100), (B): a blood vessel (V) and a bronchiole (B) lined by columnar cells and Clara cells ( ) (×400) (C): alveoli (a) lined mainly by type I pneumocytes ( ). Note few type II pneumocytes ( ) and pulmonary capillaries (c) (×1000). Lung sections in Gp III (H&E) showing (D): obvious thickening of multiple IAS ( ), a distorted bronchiole ( ) and partial thickening of the wall of a venule ( ) (×100), (E): two peribronchial mononuclear aggregates, (MA1) and (MA2). Note obvious thickening of the wall of a vessel ( ) (×100) (F): stratification of the lining epithelium ( ), shed cellular debris ( ) in the lumen of a bronchiole, a congested vessel (c). Note the lining cells with dark nuclei ( ) (×400). (G): thickened IAS harboring multiple fibroblasts (F) surrounded by collagen deposition (*). Note multiple infiltrating cells ( ) (H): multiple type II pneumocytes ( ) and few type I pneumocytes ( ). Note shed cells (*) (×1000).

  • Fig. 2 Rat lung sections in Gp IV (H&E) showing (A): 2 bronchioles with few shed epithelial cells (*) in their lumens and thickening of some IAS ( ) (×100), (B): focal stratification of the bronchiolar lining epithelium ( ) and few shed cells (*) (×400) (C): numerous type I pneumocytes ( ) and fewer type II pneumocytes ( ) (×1000). In Gp V showing (D): a bronchiole with few shed epithelial cells in the lumen (*) and few thickened IAS ( ). Note a congested vessel (c) (×100), (E): multiple spindle cells (S) in the lumen of a vessel. Note partial thickening ( ) of its wall and few round infiltrating cells in the IAS ( ) (×400) and (F): numerous type I pneumocytes ( ) and fewer type II pneumocytes ( ) (×1000).

  • Fig. 3 (A): Lung sections in Gp I showing fine collagen fibers in the IAS ( ), in the adventitia of a bronchiole ( ) and that of a venule ( ). (B): In Gp III showing dense collagen fibers deposition in thickened IAS ( ), around bronchioles ( ) and around congested blood vessels ( ). (C): In Gp IV showing minimal collagen fibers in the IAS ( ), the adventitia of a bronchiole ( ) and that of a vessel ( ). (D): In Gp V showing minimal collagen fibers in the IAS ( ), the adventitia of a bronchiole ( ) and that of a vessel ( ). (Masson’s trichrome, ×200).

  • Fig. 4 (A): In Gp I showing −ve staining with Pb in a bronchiole (B), alveoli and IAS. In Gp V showing (B): multiple Pb +ve cells surrounding ( ) and inside ( ) a congested blood vessel (c), (C): multiple Pb +ve cells ( ) in thickened IAS (Pb, ×400).

  • Fig. 5 Caspase 3 immunostaining (×400) lung sections (A): in Gp I showing an immunostained +ve cell among the epithelial lining of an alveolus ( ) and another +ve cell in the lining of a bronchiole ( ) (B): In Gp III showing multiple +ve cells in the epithelial lining of alveoli, alveolar sacs ( ) and in thickened IAS ( ) (C): In GP IV showing few +ve cells in the lining epithelium ( ) of 2 alveoli, alveolar sac and in 2 IAS ( ). (D): In GP V showing few +ve cells in the lining epithelium ( ) and adventitia (*) of a bronchiole. Note a +ve cell in the lining epithelium of an alveolus ( ). CD44 immunostaining (×400) lung sections (E): in Gp I showing −ve CD44 immunostaining among the epithelium lining a bronchiole, alveoli and alveolar sacs. (F): In Gp III showing few CD44 +ve spindle cells in obviously thickened IAS ( ) (G): In Gp IV showing multiple +ve spindle cells in thickened IAS ( ). (H): In Gp V showing multiple +ve cuboidal cells (C) and +ve spindle cells (S) among the epithelial lining of alveoli and alveolar sacs.

  • Fig. 6 Histogram comparing (A): the mean values of thickness of IAS in the control and experimental groups, (B): the mean values of thickness of wall of blood vessels in the control and experimental groups, (C): the mean values of area % of collagen fibers in the control and experimental groups, (D): the mean values of area % of caspase 3 +ve cells in the control and experimental groups, (E): the mean values of area % of CD44 +ve cells in the control and experimental groups.


Cited by  2 articles

Effect of Stem Cells, Ascorbic Acid and SERCA1a Gene Transfected Stem Cells in Experimentally Induced Type I Diabetic Myopathy
Maha B Zickri, Eman M Sadek, Amal E Fares, Nehal G Heteba, Ahmed M Reda
Int J Stem Cells. 2020;13(1):163-175.    doi: 10.15283/ijsc18066.

Effect of Stem Cells and Gene Transfected Stem Cells Therapy on the Pancreas of Experimentally Induced Type 1 Diabetes
Maha Baligh Zickri, Gihan Ibrahim Aboul-Fotouh, Abeer Ibraheem Omar, Asmaa Ahmed El-Shafei, Ahmed Mahmoud Reda
Int J Stem Cells. 2018;11(2):205-215.    doi: 10.15283/ijsc18002.


Reference

References

1. Meyer KC. Diagnosis and management of interstitial lung disease. Transl Respir Med. 2014; 2:1–13. DOI: 10.1186/2213-0802-2-4.
Article
2. Garg J, Agrawal N, Marballi A, Agrawal S, Rawat N, Sule S, Lehrman SG. Amiodarone induced pulmonary toxicity: An unusual response to steroids. Am J Case Rep. 2012; 13:62–65. DOI: 10.12659/AJCR.882757. PMID: 23569490. PMCID: 3615935.
Article
3. Mankikian J, Favelle O, Guillon A, Guilleminault L, Cormier B, Jonville-Béra AP, Perrotin D, Diot P, Marchand-Adam S. Initial characteristics and outcome of hospitalized patients with amiodarone pulmonary toxicity. Respir Med. 2014; 108:638–646. DOI: 10.1016/j.rmed.2014.01.014. PMID: 24565600.
Article
4. Minder CM, Blaha MJ, Horne A, Michos ED, Kaul S, Blumenthal RS. Evidence-based use of statins for primary prevention of cardiovascular disease. Am J Med. 2012; 125:440–446. DOI: 10.1016/j.amjmed.2011.11.013. PMID: 22387091.
Article
5. Malekinejad H, Mehrabi M, Khoramjouy M, Rezaei-Golmisheh A. Antifibrotic effect of atorvastatin on paraquat-induced pulmonary fibrosis: role of PPARγ receptors. Eur J Pharmacol. 2013; 720:294–302. DOI: 10.1016/j.ejphar.2013.10.013. PMID: 24161914.
Article
6. Labusca L, Zugun-Eloae F, Nacu V, Mashayekhi K. Adipose derived stem cells for musculoskeletal regeneration: recent patents and future perspectives. Regen Med. 2013; 3:132–147.
Article
7. Tajiri N, Acosta SA, Shahaduzzaman M, Ishikawa H, Shinozuka K, Pabon M, Hernandez-Ontiveros D, Kim DW, Metcalf C, Staples M, Dailey T, Vasconcellos J, Franyuti G, Gould L, Patel N, Cooper D, Kaneko Y, Borlongan CV, Bickford PC. Intravenous transplants of human adipose-derived stem cell protect the brain from traumatic brain injury-induced neurodegeneration and motor and cognitive impairments: cell graft biodistribution and soluble factors in young and aged rats. J Neurosci. 2014; 34:313–326. DOI: 10.1523/JNEUROSCI.2425-13.2014. PMID: 24381292. PMCID: 3866490.
Article
8. Zhu B, Ma AQ, Yang L, Dang XM. Atorvastatin attenuates bleomycin-induced pulmonary fibrosis via suppressing iNOS expression and the CTGF (CCN2)/ERK signaling pathway. Int J Mol Sci. 2013; 14:24476–24491. DOI: 10.3390/ijms141224476. PMID: 24351828. PMCID: 3876122.
Article
9. Madkour NK, Ahmed M. Amelioration of amiodarone-induced lung fibrosis in rats by grape seed extract. J Appl Sci Res. 2013; 9:3698–3707.
10. Gnanasegaran N, Govindasamy V, Musa S, Kasim NH. Different isolation methods alter the gene expression profiling of adipose derived stem cells. Int J Med Sci. 2014; 11:391–403. DOI: 10.7150/ijms.7697. PMID: 24669199. PMCID: 3964446.
Article
11. Ma T, Gong K, Ao Q, Yan Y, Song B, Huang H, Zhang X, Gong Y. Intracerebral transplantation of adipose-derived mesenchymal stem cells alternatively activates microglia and ameliorates neuropathological deficits in Alzheimer’s disease mice. Cell Transplant. 2013; 22(Suppl 1):S113–S126. DOI: 10.3727/096368913X672181.
Article
12. Koch TG, Heerkens T, Thomsen PD, Betts DH. Isolation of mesenchymal stem cells from equine umbilical cord blood. BMC Biotechnol. 2007; 7:26–34. DOI: 10.1186/1472-6750-7-26. PMID: 17537254. PMCID: 1904213.
Article
13. Wei Y, Gong K, Zheng Z, Wang A, Ao Q, Gong Y, Zhang X. Chitosan/silk fibroin-based tissue-engineered graft seeded with adipose-derived stem cells enhances nerve regeneration in a rat model. J Mater Sci Mater Med. 2011; 22:1947–1964. DOI: 10.1007/s10856-011-4370-z. PMID: 21656031.
Article
14. Kraitchman DL, Heldman AW, Atalar E, Amado LC, Martin BJ, Pittenger MF, Hare JM, Bulte JW. In vivo magnetic resonance imaging of mesenchymal stem cells in myocardial infarction. Circulation. 2003; 107:2290–2293. DOI: 10.1161/01.CIR.0000070931.62772.4E. PMID: 12732608.
Article
15. Strober W. Trypan blue exclusion test of cell viability. Curr Protoc Immunol. 2001; DOI: 10.1002/0471142735.ima03bs21.
Article
16. Osanai K, Higuchi J, Oikawa R, Kobayashi M, Tsuchihara K, Iguchi M, Huang J, Voelker DR, Toga H. Altered lung surfactant system in a Rab38-deficient rat model of Hermansky-Pudlak syndrome. Am J Physiol Lung Cell Mol Physiol. 2010; 298:L243–L251. DOI: 10.1152/ajplung.00242.2009.
Article
17. Kiernan JK. Histological and histochemical methods. Theory and practice. 3rd ed. London, New York, New Delhy: Arnold Publisher;2001. p. 111–162.
18. Suvarna KS, Layton C, Bancroft JD. Pigments and minerals. Bancroft’s theory and practice of histological techniques. 7th ed. Oxford, UK, China: Churchill Livingstone Elsevier;2013. p. 241–242.
19. Ellis R. Perl’s prussian blue stain protocol. South Australia: Pathology Division, Queen Elizabeth Hospital;2007.
20. Sun W, Su Q, Cao X, Shang B, Chen A, Yin H, Liu B. High expression of polo-like kinase 1 is associated with early development of hepatocellular carcinoma. Int J Genomics. 2014; 2014:312130. DOI: 10.1155/2014/312130. PMID: 25019081. PMCID: 4074973.
Article
21. Li L, Xia Y. Study of adipose tissue-derived mesenchymal stem cells transplantation for rats with dilated cardiomyopathy. Ann Thorac Cardiovasc Surg. 2014; 20:398–406. DOI: 10.5761/atcs.oa.13-00104. PMID: 24492176.
Article
22. Barker AF, Bergeron A, Rom WN, Hertz MI. Obliterative bronchiolitis. N Engl J Med. 2014; 370:1820–1828. DOI: 10.1056/NEJMra1204664. PMID: 24806161.
Article
23. Grommes J, Soehnlein O. Contribution of neutrophils to acute lung injury. Mol Med. 2011; 17:293–307. DOI: 10.2119/molmed.2010.00138. PMCID: 3060975.
Article
24. Shroff A, Mamalis A, Jagdeo J. Oxidative stress and skin fibrosis. Curr Pathobiol Rep. 2014; 2:257–267. DOI: 10.1007/s40139-014-0062-y. PMID: 25401052. PMCID: 4223577.
Article
25. Valcheva-Kuzmanova S, Stavreva G, Dancheva V, Terziev L, Atanasova M, Stoyanova A, Dimitrova A, Shopova V. Effect of Aronia melanocarpa fruit juice on amiodarone-induced pneumotoxicity in rats. Pharmacogn Mag. 2014; 10:132–140. DOI: 10.4103/0973-1296.131024. PMID: 24914278. PMCID: 4048559.
Article
26. Lee TH, Sottile J, Chiang HY. Collagen inhibitory peptide R1R2 mediates vascular remodeling by decreasing inflammation and smooth muscle cell activation. PLoS One. 2015; 10:e0117356. DOI: 10.1371/journal.pone.0117356. PMID: 25675397. PMCID: 4326127.
Article
27. Gumuser G, Vural K, Varol T, Parlak Y, Tuglu I, Topal G, Sayit E. Assessment of lung toxicity caused by bleomycin and amiodarone by Tc-99m HMPAO lung scintigraphy in rats. Ann Nucl Med. 2013; 27:592–599. DOI: 10.1007/s12149-013-0722-8. PMID: 23558450. PMCID: 3742950.
Article
28. Selman M, Vicens V, Mendoza C, Montaño M, Ramos C, Romero Y, Molina M. Subsets of fibroblasts show resistance to apoptosis independently of their interstitial lung disease origin. FASEB J. 2013; 27:1166.4.
Article
29. Lee J, Hong EM, Koh DH, Choi MH, Jang HJ, Kae SH, Choi HS. HMG-CoA reductase inhibitors (statins) activate expression of PPARalpha/PPARgamma and ABCA1 in cultured gallbladder epithelial cells. Dig Dis Sci. 2010; 55:292–299. DOI: 10.1007/s10620-009-0734-3.
Article
30. Khodayar MJ, Kiani M, Hemmati AA, Rezaie A, Zerafatfard MR, Rashidi Nooshabadi MR, Goudarzi M. The preventive effect of atorvastatin on paraquat-induced pulmonary fibrosis in the rats. Adv Pharm Bull. 2014; 4:345–349. PMID: 25436189. PMCID: 4137423.
31. Zhang Y, Dai L, Wu S, Chen P, Zhao S. Atorvastatin attenuates involvement of RhoA/Rho-kinase pathway and NF-κB activation in hypoxic pulmonary hypertensive rats. Chin Med J (Engl). 2014; 127:869–872.
32. Chen ZY, Liu SN, Li CN, Sun SJ, Liu Q, Lei L, Gao LH, Shen ZF. Atorvastatin helps preserve pancreatic β cell function in obese C57BL/6 J mice and the effect is related to increased pancreas proliferation and amelioration of endoplasmic-reticulum stress. Lipids Health Dis. 2014; 13:98. DOI: 10.1186/1476-511X-13-98.
33. Ghasemi N. Therapeutic effects of adipose derived mesenchymal stem cells on remyelination process in inflammatory demyelinating diseases. J Histol Histopathol. 2015; 2:8. DOI: 10.7243/2055-091X-2-8.
Article
34. Abd El Azeem AF, Al-Ahmadyb HM, Abdul Rahmana MA, Abdel Hameed MA, Shaalan OF. Angiogenesis induced by autologous whole bone marrow stem cells seeded on collagen scaffolds in silicone nerve tubes. An experimental study. Tanta Dental J. 2014; 111:227–234. DOI: 10.1016/j.tdj.2014.10.006.
Article
35. Linero I, Chaparro O. Paracrine effect of mesenchymal stem cells derived from human adipose tissue in bone regeneration. PLoS One. 2014; 9:e107001. DOI: 10.1371/journal.pone.0107001. PMID: 25198551. PMCID: 4157844.
Article
36. Castiglione F, Hedlund P, Van der Aa F, Bivalacqua TJ, Rigatti P, Van Poppel H, Montorsi F, De Ridder D, Albersen M. Intratunical injection of human adipose tissue-derived stem cells prevents fibrosis and is associated with improved erectile function in a rat model of Peyronie’s disease. Eur Urol. 2013; 63:551–560. DOI: 10.1016/j.eururo.2012.09.034.
Article
37. Wang WW, Li ZZ, Wang W, Jiang Y, Cheng J, Lu S, Zhang JY. Enhanced renoprotective effect of HIF-1α modified human adipose-derived stem cells on cisplatin-induced acute kidney injury in vivo. Sci Rep. 2015; 5:10851. DOI: 10.1038/srep10851.
Article
38. Albersen M, Berkers J, Dekoninck P, Deprest J, Lue TF, Hedlund P, Lin CS, Bivalacqua TJ, Van Poppel H, De Ridder D, Van der Aa F. Expression of a distinct set of chemokine receptors in adipose tissue-derived stem cells is responsible for in vitro migration toward chemokines appearing in the major pelvic ganglion following cavernous nerve injury. Sex Med. 2013; 1:3–15. DOI: 10.1002/sm2.1. PMID: 25356281. PMCID: 4184711.
Article
39. Ding Z, Huang H. Mesenchymal stem cells in rabbit meniscus and bone marrow exhibit a similar feature but a heterogeneous multi-differentiation potential: superiority of meniscus as a cell source for meniscus repair. BMC Musculoskelet Disord. 2015; 16:65. DOI: 10.1186/s12891-015-0511-8. PMID: 25887689. PMCID: 4373281.
Article
40. Williams AR, Hare JM. Mesenchymal stem cells: biology, pathophysiology, translational findings, and therapeutic implications for cardiac disease. Circ Res. 2011; 109:923–940. DOI: 10.1161/CIRCRESAHA.111.243147. PMID: 21960725. PMCID: 3604746.
Full Text Links
  • IJSC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr