Literature DB >> 29285566

Suppression of aortic expansion and contractile recovery in a rat abdominal aortic aneurysm model by biodegradable gelatin hydrogel sheet incorporating basic fibroblast growth factor.

Norikazu Kawai1, Hisashi Iwata2, Katsuya Shimabukuro1, Narihiro Ishida1, Hiroki Ogura1, Etsuji Umeda1, Kiyoshi Doi1.   

Abstract

Biodegradable gelatin hydrogel sheet (BGHS) incorporating basic fibroblast growth factor (bFGF) may inhibit the progression of abdominal aortic aneurysm (AAA). We investigated whether AAA in a rat model treated with BGHS soaked with bFGF can suppress aortic expansion and recover the contractile response of aneurysmal aortic wall. Experimental AAA was induced in 10-week-old male Sprague-Dawley rats with intra-aortic elastase infusion. Aortas of these rats were assigned to 4 groups (n = 6 each) as follows: Control group, aortas infused with saline; Elastase only group, aortas infused with elastase; Hydrogel group, aortas wrapped with saline-soaked BGHS after elastase infusion; and bFGF group, aortas wrapped with bFGF (100 μg)-soaked BGHS after elastase infusion. Preoperatively and on postoperative day (POD)7 and POD14, mean aortic maximal diameter was measured ultrasonographically. Aortic expansion ratio was calculated as: (post-infusion aortic diameter on POD14/pre-infusion aortic diameter × 100). Aortas were stained with Elastica van Gieson and α-smooth muscle actin to measure the ratio of elastic fibers and α-smooth muscle actin-positive cells area to the media area. Aortas on POD14 were cut into 2-mm rings and treated with contractile agent, then tension was recorded using myography. Maximum aorta diameters were significantly greater in Elastase only group, Hydrogel group, and bFGF group than in Control group (on POD14). Maximum diameter was significantly lower in bFGF group (3.52 ± 0.4 mm) than in Elastase only group (6.21 ± 1.4 mm on POD14, P < .05). On histological analysis, ratio of the area staining positively for elastic fibers was significantly greater in bFGF group (7.43 ± 1.8%) than in Elastase only group (3.76 ± 2.9%, P < .05). The ratio for α-smooth muscle actin-positive cells was significantly lower in Elastase only group (38.3 ± 5.1%) than in Control group (49.8 ± 6.7%, P < .05). No significant differences were seen between Elastase only group and bFGF group, but ratios tended to be increased in bFGF group. Consecutive mean contractile tensions were significantly higher in bFGF group than in Elastase only group. Maximum contractile tension was significantly higher in bFGF group (1.3 ± 0.4 mN) than in Elastase only group (0.4 ± 0.2 mN, P < .05). Aortic expansion can be suppressed and contractile responses of aneurysmal aortic wall recovered using BGHS incorporating bFGF.

Entities:  

Keywords:  Abdominal aortic aneurysm; Angiogenesis; Basic fibroblast growth factor; Vascular function

Mesh:

Substances:

Year:  2017        PMID: 29285566     DOI: 10.1007/s00380-017-1114-0

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  27 in total

1.  Gelatin sheet incorporating basic fibroblast growth factor enhances sternal healing after harvesting bilateral internal thoracic arteries.

Authors:  Atsushi Iwakura; Yasuhiko Tabata; Tadaaki Koyama; Kazuhiko Doi; Kazunobu Nishimura; Kazuaki Kataoka; Masatoshi Fujita; Masashi Komeda
Journal:  J Thorac Cardiovasc Surg       Date:  2003-10       Impact factor: 5.209

Review 2.  Late Rupture of Abdominal Aortic Aneurysm After Previous Endovascular Repair: A Systematic Review and Meta-analysis.

Authors:  George A Antoniou; George S Georgiadis; Stavros A Antoniou; Simon Neequaye; John A Brennan; Francesco Torella; S Rao Vallabhaneni
Journal:  J Endovasc Ther       Date:  2015-08-18       Impact factor: 3.487

Review 3.  Mechanical, biochemical, and extracellular matrix effects on vascular smooth muscle cell phenotype.

Authors:  Jan P Stegemann; Helen Hong; Robert M Nerem
Journal:  J Appl Physiol (1985)       Date:  2005-06

4.  Biomechanical properties of ruptured versus electively repaired abdominal aortic aneurysm wall tissue.

Authors:  Elena S Di Martino; Ajay Bohra; Jonathan P Vande Geest; Navyash Gupta; Michel S Makaroun; David A Vorp
Journal:  J Vasc Surg       Date:  2006-03       Impact factor: 4.268

Review 5.  Vascular mechanics for the cardiologist.

Authors:  R T Lee; R D Kamm
Journal:  J Am Coll Cardiol       Date:  1994-05       Impact factor: 24.094

6.  Controlled release of growth factors based on biodegradation of gelatin hydrogel.

Authors:  M Yamamoto; Y Ikada; Y Tabata
Journal:  J Biomater Sci Polym Ed       Date:  2001       Impact factor: 3.517

7.  Effects of chronic systemic administration of basic fibroblast growth factor on collateral development in the canine heart.

Authors:  D F Lazarous; M Scheinowitz; M Shou; E Hodge; S Rajanayagam; S Hunsberger; W G Robison; J A Stiber; R Correa; S E Epstein
Journal:  Circulation       Date:  1995-01-01       Impact factor: 29.690

Review 8.  Inflammation and cellular immune responses in abdominal aortic aneurysms.

Authors:  Koichi Shimizu; Richard N Mitchell; Peter Libby
Journal:  Arterioscler Thromb Vasc Biol       Date:  2006-02-23       Impact factor: 8.311

9.  The impact of endovascular aneurysm repair on mortality for elective abdominal aortic aneurysm repair in England and the United States.

Authors:  Alan Karthikesalingam; Peter J Holt; Alberto Vidal-Diez; Sandeep S Bahia; Benjamin O Patterson; Robert J Hinchliffe; Matthew M Thompson
Journal:  J Vasc Surg       Date:  2016-04-01       Impact factor: 4.268

Review 10.  The efficacy of pharmacotherapy for decreasing the expansion rate of abdominal aortic aneurysms: a systematic review and meta-analysis.

Authors:  Idris Guessous; Daniel Periard; Diane Lorenzetti; Jacques Cornuz; William A Ghali
Journal:  PLoS One       Date:  2008-03-26       Impact factor: 3.240

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