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(Circulation. 2000;102:III-307.)
© 2000 American Heart Association, Inc.
Myocardial Protection and Vascular Biology |
Novel Method to Enhance Sternal Healing After Harvesting Bilateral Internal Thoracic Arteries With Use of Basic Fibroblast Growth Factor
From the Department of Cardiovascular Surgery (A. Iwakura, N.T., A. Ikai, K.N., M.K.), Kyoto University Graduate School of Medicine, and the Institute for Frontier Medical Sciences (Y.T., M.M., M.O., T.N., Y.S.) and College of Medical Technology (M.F.), Kyoto University, Kyoto, Japan.
Correspondence to Masashi Komeda, MD, Professor and Chairman, Department of Cardiovascular Surgery, Kyoto University, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, Japan 606-8507. E-mail masakom{at}kuhp.kyoto-u.ac.jp
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Abstract |
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Background—Poor healing of the sternum often limits the use of bilateral internal thoracic arteries (BITAs) in coronary bypass surgery, especially for diabetic patients. We have reported that basic fibroblast growth factor (bFGF) enhanced regeneration of the skull. This study was designed to evaluate the effects of topical use of bFGF on sternal healing after removing the BITAs.
Methods and Results—Forty-five Wistar rats were subjected to median sternotomy and were divided into 3 groups: 15 had the BITAs removed and had a bFGF sheet applied on the posterior table of the sternum (group A), 15 had just the BITAs removed (group B), and 15 had intact BITAs (group C). Five and 10 rats were euthanized 2 and 4 weeks after surgery, respectively, in all 3 groups. Peristernal blood flow, measured with use of a noncontact laser flowmeter, decreased after removal of the BITAs (P<0.001). Four weeks after the surgery, PBF markedly increased only in group A (9.7±1.2, 6.5±0.6, and 8.2±0.5 mL · min-1 · 100 g-1 for groups A, B, and C, respectively; P<0.01 by ANOVA). Four weeks after surgery, the following findings were obtained only in group A: (1) nearly completely healed sternum filled with regenerated bone tissue, (2) marked angiogenesis around the sternum, and (3) osteoblasts in an active form around the edge of the sternum.
Conclusions—The results suggest that use of the bFGF sheet offset the sternal ischemia and accelerated sternal healing. This method may help to decrease sternal necrosis in high-risk patients or allow extended use of BITAs in coronary bypass surgery.
Key Words: angiogenesis • blood flow • growth substances
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Introduction |
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Slow or poor healing of the sternum is one of the potential problems encountered after sternotomy and is therefore one of the potential problems associated with heart surgery. Slow healing prolongs the patients’ hospital stay, increases health care costs considerably, and delays the patients’ return to work or social activities. Poor healing of the sternum often leads to deep sternal wound infection, which is serious.1 2 3 Previous studies have identified risk factors for sternal wound complications, such as obesity, chronic obstructive pulmonary disease, elderly age, peripheral vascular disease, reoperation, diabetes mellitus, use of internal thoracic artery (ITA) conduits, prolonged operation time, low cardiac output, prolonged ventilation time, and reexploration for bleeding.4 5 6 The number of patients with some of the above risk factors is increasing, and slow/poor sternal healing will become even more problematic in this population. Slow/poor healing often limits the use of bilateral internal thoracic arteries (BITAs) in coronary bypass surgery, especially in diabetic patients whose hearts are shown to benefit from BITA grafting,7 because diabetic patients are more prone to sternal necrosis, particularly after removal of the BITAs because of the lack of blood supply.
It has been reported that basic fibroblast growth factor (bFGF) is not only a potent angiogenic mitogen but also an effector that can stimulate bone formation.8 However, when bFGF is injected in free form, it does not stay at the injection site for a period long enough for its effective biological activity to produce the expected results. In an attempt to solve this problem, we developed a biodegradable hydrogel composed of acidic gelatin to enable bFGF to be released at the site of action for an extended time period. We have demonstrated that gelatin hydrogels, with incorporated bFGF, enhanced in vivo bone regeneration in the skull. The purpose of the present study was to evaluate the effect of topical use of bFGF on sternal healing after the removal of BITAs in rats.
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Methods |
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Preparation of bFGF-Incorporated Gelatin Hydrogel Sheets
Gelatin with an isoelectric point of 4.9 was isolated from bovine bone collagen by an alkaline process using Ca(OH)2 (Nitta Gelatin Co). The weight-average molecular weight of the gelatin was 99 000 when measured by gel filtration chromatography relative to standard polyethylene glycol samples. Human recombinant bFGF with an isoelectric point of 9.6 was obtained from Kaken Pharmaceutical Co.
Gelatin in 10 wt% aqueous solution was chemically cross-linked with various amounts of glutaraldehyde at 25°C to prepare sheets with different extents of cross-linking. Briefly, 4.5 mL of an aqueous gelatin solution containing glutaraldehyde was cast into a polytetrafluoroethylene mold (5x5 cm2, 1.8-mm depth). After the cross-linking reaction, which lasted for 12 hours at 25°C, the resulting hydrogel sheets were immersed in 50 mmol/L of glycine aqueous solution at 37°C for 1 hour to block residual aldehyde groups of glutaraldehyde, then rinsed with double-distilled water and 100% ethanol, and autoclaved while immersed in double-distilled water to obtain sterilized sheets. These were freeze-dried, followed by impregnation with an aqueous solution containing 100 µg of bFGF, to obtain gelatin hydrogels with incorporated bFGF. The prepared hydrogel sheets were rectangle-shaped (1x10 mm) and 0.7-mm thick. All experimental processes were conducted under sterile conditions.
Animal Experiments
Forty-five male Wistar rats weighing between 300 and 400 g
were orally intubated after anesthesia with use of a small
amount of 99.5% ether and were ventilated on a small volume-cycled
animal ventilator (rodent ventilator model 683, Harvard
Apparatus). Anesthesia was maintained during
the operation with 1% to 2% isoflurane. After a midline skin
incision, with the animal in the supine position, the bilateral major
pectoral muscles were divided from the junction of the sternum, and
intercostal muscles on both sides of the sternum were exposed. Median
sternotomy was carefully performed by using a rotating saw (D-7200,
AESCULAP), leaving part of the narrow sternum on
both sides. The bleeding from the bone marrow was stopped through the
use of bone wax (Nestor, Nippon Shoji). The 45 rats were randomly
divided into 3 groups: group A (n=15) had the BITAs removed, and a
gelatin hydrogel sheet with incorporated bFGF was placed on the
posterior table of the sternum before closing the sternum; group B
(n=15) had the BITAs removed, and the sternum was closed without using
the sheet; and group C (n=15) had the BITAs left intact, and the
sternum was closed without the sheet. For removal of the BITAs (ie, in
groups A and B), they were ligated using 6-0 polypropylene sutures near
the origin and at the distal bifurcation, and the BITAs, with their
beds, were destroyed by use of an electrical coagulator. When the
gelatin hydrogel sheets with incorporated bFGF (100 µg per sheet)
were placed in the animals in group A, the ITA beds were also covered
by the sheet, and the sheet was stabilized with 6-0 polypropylene
sutures. After positive end-expiratory pressure was applied to fully
inflate the lung, the sternum was parasternally closed with 4
interrupted braided polyester sutures. The muscle layer and the skin
were carefully sutured with 4-0 nylon monofilaments. Streptomycin was
administered intramuscularly just after skin closure (50 mg per rat).
Rats were euthanized by intravenous administration of a
lethal dose of sodium pentobarbital for 2 weeks (5 animals in each
group) and 4 weeks (10 animals in each group) after the surgery. The
sternum was excised and fixed in 10 wt% formaldehyde solution in PBS
for 4 days for assessment of the extent of bone regeneration. All the
animal experiments were performed according to the institutional
guidelines for animal experimentation of Kyoto University.
Measurement of PBF
Peristernal blood flow (PBF, ml ·
min-1 · 100 g-1)
at the capillary blood perfusion level was measured with use of a
noncontact laser flowmeter (ALF21N, Advance) before the median
sternotomy, after closure of the sternum, and 2 and 4 weeks after the
surgery. A beam of laser light was directed through an optic fiber to a
measuring probe with a diameter of 3.0 mm. The probe was placed
over the intercostal muscles near the sternum, separated by 10 mm
in a straight line so that the area of measurement was 
5 mm in
diameter and 1 mm in depth. The He-Ne light was then switched to a
diode laser (2 mW, 780 nm) to measure PBF, which was calculated on the
basis of the Doppler shift.9 The probe included 2
optic fibers, one for laser illumination and the other for receiving
reflected and dispersed light. Three readings for each measurement were
recorded after a stable baseline had been obtained, and the 3
values were averaged.
Histological Assessment of Angiogenesis
Arterioles (>25 and <100 µm in external diameter) and
capillaries (
25 µm in external diameter) were counted in
preparations stained with hematoxylin-eosin. Five fields were randomly
chosen from the connective tissue around the sternum. Two pathologists
without knowledge of the treatments counted the number of vessels per
unit area (200x200 µm2) by using a grid
method10 whereby the density of arterioles in each
5-mmx5-mm field was assessed by determining the mean number of vessels
in 5 randomly chosen unit areas (200 µmx200 µm) with use
of a section ocular micrometer (Olympus) at x400
magnification. The total number of vessels in the 25 unit areas (5
fields with 5 unit areas per field) was counted and averaged. To
maintain randomness, an optic lens containing a protractor and
micrometer was used for selection of the 5 portions.
Assessment of Bone Formation
Bone regeneration in the sternum was assessed by soft x-ray
analysis and histological examination. Soft
(high-contrast) x-ray pictures of the sternum were taken at 46 kV and 2
mA for 45 seconds by use of an x-ray apparatus (type CMB,
Koizumi X-Senkosha). Photographs of formalin-fixed bone specimens from
different experimental groups were taken with the use of the same type
of x-ray film.
Bone specimens were demineralized in 10 wt% EDTA solution at 4°C for 3 days, embedded in paraffin, and sectioned at 10-µm thickness. The sections were obtained at the third, fourth, and fifth intercostal spaces of the sternum and stained with hematoxylin-eosin 2 and 4 weeks after the surgery. The histological sections were analyzed by use of a microscope equipped with a video camera connected to an image analysis system (SP-1000, Olympus). The area of new bone in each section prepared from the sternum was measured at x2 magnification. To observe the osteoblasts in active form, which are characterized by a basophilic cuboid cytoplasm located adjacent to the bone surface, and osteoclasts that have a basophilic cytoplasm and plural nuclei, the histological sections were viewed at high magnification (x400) with a light microscope.
Statistical Analysis
All of the data were analyzed by 1-way ANOVA to assess
the statistical significance among experimental groups. Experimental
results were expressed as mean±SD. Results of the statistical
analyses were regarded as significant at a value of
P<0.05.
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Results |
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TopAbstractIntroductionMethodsResultsDiscussionReferences |
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Peristernal Blood Flow
Preoperative PBF was 8.6±0.6 (mean±SD) mL · min-1 · 100 g-1. Although the PBF did not change after the median sternotomy alone (ie, intact BITAs), it was significantly reduced to 4.2±0.6 mL · min-1 · 100 g-1 after removal of the BITAs (P<0.001). PBF 2 weeks after the surgery in group A and group B was 6.5±0.7 and 5.9±0.55 mL · min-1 · 100 g-1, respectively, both of which were significantly lower than that in group C (8.0±0.7 mL · min-1 · 100 g-1). However, 4 weeks after surgery in groups A, B, and C, PBF was 9.7±1.2, 6.5±0.6, and 8.2±0.5 mL · min-1 · 100 g-1, respectively. Significant differences were noted among the 3 groups (P<0.01). Results for PBF before and after median sternotomy with different surgeries in each group are summarized in Figure 1
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Histological Assessment of Angiogenesis
Histological examination of the tissue around the
sternum confirmed that there was an increase in the number of vessels.
Photomicrographs of the connective tissue around the sternum 4 weeks
after surgery are shown in Figure 2.
There were more capillaries and arterioles (10 to 50 µm in
diameter) around the sternum in group A than in group B or C (Figure 2). Figure 3 shows the number of
arterioles and capillaries per unit area around the sternum 4 weeks
after surgery in each of the 3 groups. In group A, a larger number of
vessels was seen in the connective tissue around the sternum. On the
other hand, in groups B and C, significantly lower numbers of vessels
were noted. The number of the arterioles and the number of capillaries
per unit area around the sternum increased to a greater extent in group
A than in the other 2 groups (30.5±3.2, 15.8±2.7, and 12.3±1.5
vessels per unit area for groups A, B, and C, respectively;
P<0.01).
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Assessment of Bone Formation
Soft x-ray photographs of the sternum 4 weeks after the different
surgeries are shown in Figure 4.
Dehiscence of the separated original sternum was observed in group B.
In contrast, groups A and C had no sternal dehiscence. Almost complete
bone regeneration was seen in group A only.
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Figure 5 shows
histological sections of the sternum 2 and 4 weeks
after surgery with the different procedures. Two weeks after surgery,
histological examination showed that new cartilage had
formed around the sternum in all groups. At this time, a little
intracartilaginous ossification around the original sternum was
observed in group A (Figure 5A1) and group C (Figure 5C1)
but not in group B (Figure 5B1). Four weeks after the surgery,
groups B and C had partial intracartilaginous ossification around the
original sternum (Figure 5B2 and 5C2). In contrast, in group A,
the sternum had nearly completely healed and was filled with
regenerated bone tissue and bone marrow (Figure 5A2). Many
osteoblasts were seen in active form at the border zone between the
regenerated cartilage and the cancellous bone; moreover, osteoclasts
were found to erode the matured cancellous bone, which had bone
marrow.
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The area of new bone formation of the sternum in each group 2 and 4
weeks after surgery was analyzed quantitatively, and the
results are shown in Figure 6. Two weeks
after surgery, the area of new bone formation in group A tended to be
larger than in group B or C, but the differences among the 3 groups
were not statistically significant (1.79±1.22, 0.87±0.70, and
1.37±0.92 mm2 for groups A, B, and C,
respectively). Four weeks after the surgery, however, group A had a
significantly larger area of new bone formation than did the other 2
groups (5.13±2.82, 2.17±0.91, and 2.01± 0.89
mm2 for groups A, B, and C, respectively).
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Discussion |
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Several clinical and experimental studies have demonstrated a decrease in sternal blood flow after ITA harvesting. Arnold11 reported that BITA mobilization may render the sternum avascular; he studied 52 human sternal specimens by postoperative radioisotope angiography with use of a radioactive microsphere technique. Results of the study by Arnold were supported by the results of Seyfer et al,12 who measured sternal blood flow in rhesus monkeys with the use of microspheres. The blood flow was unchanged after median sternotomy alone, but mobilization of the unilateral ITA decreased sternal blood flow by 90%. Recently, using radioactive microspheres, Parish et al13 demonstrated that chest wall blood flow was significantly decreased compared with the preharvest level after ITA mobilization in a canine model. Our results of PBF as measured by means of a noncontact laser Doppler flowmeter were consistent with the foregoing experimental studies, suggesting that the small animal model examined in the present study is compatible with the large animal model.
Our histological study of the blood vessels around the sternum showed an increase in the number of vessels, suggesting that increased PBF in group A (ie, in which a bFGF-containing gelatin hydrogel sheet was applied) is associated with the angiogenic effect of bFGF.14 Some clinical trials have suggested that harvesting the ITA conduits in a skeletonized compared with a pedicled fashion could reduce the sternal devascularization.15 16 However, there are wide variations of the anatomy of the collateral vessels around the ITA; Jesus and Acland17 classified the collaterals into 6 types in a human anatomic study. In some types in which collaterals from the lateral chest wall to the ITA connect to the anterior wall of the ITA via a common vertical channel, the collaterals from the chest wall to the sternum can be potentially preserved by careful skeletonization of the ITA (ie, if the common vertical channel alone served). However, if the collaterals connect to the side wall of the ITA (ie, no common vertical channel), even careful skeletonization can destroy the collaterals from the lateral chest wall to the sternum.
Among the many growth factors recently reported to regulate bone
metabolism, bFGF is recognized as a potent mitogen for a
variety of mesenchymal cells.18 In skeletal tissues, bFGF
is produced by cells of the osteoblastic lineage, accumulating in the
bone matrix, and it acts as an autocrine/paracrine factor for bone
cells. bFGF variably regulates the proliferation and differentiation of
cells of the osteoblastic lineage and thereby modulates the formation
of bone. Although bFGF has both angiogenic and osteogenic effects as
described above, its activity does not last long enough to show an
effect in vivo, in terms of enhancing bone regeneration, if bFGF is
given in a free form. Thus, we prepared a biodegradable hydrogel
composed of alkaline-processed "acidic" gelatin, which could
ionically interact with bFGF. Previously, we reported that such
hydrogels enabled the sustained release of biologically active bFGF
through hydrogel degradation.19 The residual radioactivity
of 125I-labeled bFGF-incorporated gelatin
hydrogels inserted into the mouse back decreased with time and remained
at the therapeutic level for 30 days after implantation.
Results of the histological examination suggested that the gelatin hydrogel sheet with incorporated bFGF helped to facilitate the bone regeneration seen 2 and 4 weeks after the surgery and that the sheet helped to increase the number of osteoblasts in active form around the sternal perimeter. The results are basically compatible with those of our previous study involving treatment of a defect of the skull in rabbits; the number of osteoblasts in active form increased during the initial 2 weeks regardless of bFGF treatment, but 12 weeks after the surgery, the increase was maintained only in the bFGF-treated group.20 In our previous study, we evaluated the effects of gelatin hydrogel alone on bone regeneration, but it was not effective in enhancing bone formation in the area of the skull defect. In the histological examination in present study, many osteoblasts in active form were observed at the site of regenerating bone as well as in the hyaline cartilage before intracartilaginous ossification only in the bFGF-treated group. We believe that enhanced regeneration of the sternum seen in the present study is also associated with the activation of osteoblasts 4 weeks after surgery through treatment with the gelatin hydrogel sheet with incorporated bFGF.
There were some limitations in this experimental study. The collateral blood supply to the sternum in rats may be different from that in humans. In fact, in rats, the highest intercostal artery is branched from the costocervical trunk, which may provide intercostal collateral flow through the periosteal plexus. However, the PBF in the present study is compatible with the sternal blood flow in our previous study that made use of a large animal model. In the present study, the area of newly generated bone 4 weeks after surgery was similar between the rats with and without BITA removal, in spite of the difference in PBF as measured with the use of a noncontact laser Doppler flowmeter. It is possible that the periosteal blood flow around the sternum was similar with or without BITA removal and that PBF reflected not only the blood flow in the periosteum but also that in the connective tissue and intercostal muscle. Further investigation with a larger animal as a model that has anatomic features similar to those of humans is necessary. Another limitation is that the histological analysis of bone formation was not precisely quantitative, because we examined the bone area in only 3 sections of the sternum in each of the groups. A quantitative analysis of the whole sternum is necessary in future investigations.
In conclusion, after sternotomy with BITA removal in the rat model, use of the gelatin hydrogel sheet with incorporated bFGF offset sternal ischemia and facilitated its healing, probably because of the angiogenic and osteogenic effects of bFGF. This method may help to decrease the chance of sternal necrosis in high-risk patients and thus can potentially extend the use of BITAs in coronary bypass surgery.
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