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Original Article

Attenuation of cyclophosphamide-induced pulmonary toxicity in Swiss albino mice by naphthalimide-based organoselenium compound 2-(5-selenocyanatopentyl)-benzo[de]isoquinoline 1,3-dione

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Pages 524-532 | Received 11 Apr 2014, Accepted 27 May 2014, Published online: 04 Dec 2014

Figures & data

Figure 1. Synthesis of compound 4, reagents, and conditions: (i) H2N(CH2)5OH, water, reflux, (ii) PBr3, ethyl acetate, and (iii) KSeCN, acetone, room temperature.

Figure 1. Synthesis of compound 4, reagents, and conditions: (i) H2N(CH2)5OH, water, reflux, (ii) PBr3, ethyl acetate, and (iii) KSeCN, acetone, room temperature.

Figure 2. Effect of compound 4 on pulmonary ROS level (A) and pulmonary NO level (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 2. Effect of compound 4 on pulmonary ROS level (A) and pulmonary NO level (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 3. Effect of compound 4 on pulmonary LPO level (A) and pulmonary GSH level (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 3. Effect of compound 4 on pulmonary LPO level (A) and pulmonary GSH level (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 4. Effect of compound 4 on pulmonary GST activity (A) and pulmonary SOD activity (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 4. Effect of compound 4 on pulmonary GST activity (A) and pulmonary SOD activity (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 5. Effect of compound 4 on pulmonary CAT activity (A) and pulmonary GPx activity (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 5. Effect of compound 4 on pulmonary CAT activity (A) and pulmonary GPx activity (B) after administration of CP. Data are represented as mean ± SD. (a) Significant (p < 0.05) as compared with Gr. I; (b) significant (p < 0.05) as compared with Gr. II; (c) significant (p < 0.05) as compared with Gr. III; (d) significant (p < 0.05) as compared with Gr. IV.

Figure 6. Photomicrographs of lung sections of mice stained with hematoxylin and eosin, 200 × ; (A) normal histology of lung with normal alveolar architecture without any epithelial damage in Gr. I; (B) normal histological features of lung in Gr. II; (C) alveolar damage, thickening of alveolar septa, and fibrous tissue proliferation in Gr. III; (D) pulmonary congestion and pulmonary inflammation in Gr. III; (E) mild to moderate thickening of alveoli, moderate reduction in alveolar distortion, and fibrous tissue proliferation in Gr. IV; (F) almost normal appearance of lung histology with no or very slight thickening of alveolar septa and no indication of fibrous tissue proliferation in Gr. V.

Figure 6. Photomicrographs of lung sections of mice stained with hematoxylin and eosin, 200 × ; (A) normal histology of lung with normal alveolar architecture without any epithelial damage in Gr. I; (B) normal histological features of lung in Gr. II; (C) alveolar damage, thickening of alveolar septa, and fibrous tissue proliferation in Gr. III; (D) pulmonary congestion and pulmonary inflammation in Gr. III; (E) mild to moderate thickening of alveoli, moderate reduction in alveolar distortion, and fibrous tissue proliferation in Gr. IV; (F) almost normal appearance of lung histology with no or very slight thickening of alveolar septa and no indication of fibrous tissue proliferation in Gr. V.

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