Histomorphometric assessment of bone necrosis produced by two cryosurgery protocols using liquid nitrogen: an experimental study on rat femurs

ORIGINAL ARTICLES

Histomorphometric assessment of bone necrosis produced by two cryosurgery protocols using liquid nitrogen: an experimental study on rat femurs

Fábio Wildson Gurgel Costa^I; Gerly Anne de Castro Brito^II; Rosana Maria Andrade Pessoa^III; Eduardo Costa Studart-Soares^IV

^IDDS, MSc, Assistant Professor, Division of Stomatology, Department of Clinical Dentistry, Federal University of Ceará, Sobral, CE, Brazil

^IIMD, MSc, PhD, Associate Professor, Division of Histology, Department of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil

^IIIDDS, Graduate student, Division of Oral Surgery, Department of Clinical Dentistry, Federal University of Ceará, Fortaleza, CE, Brazil

^IVDDS, MSc, PhD, Associate Professor, Division of Oral Surgery, Department of Clinical Dentistry, Federal University of Ceará, Fortaleza, CE, Brazil

^{Corresponding address}

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate the effects of liquid nitrogen cryosurgery on the femoral diaphysis of rats.

MATERIAL AND METHODS: The femoral diaphyses of 42 Wistar rats were exposed to three local and sequential applications of liquid nitrogen for 1 or 2 min, intercalated with periods of 5 min of passive thawing. The animals were sacrificed after 1, 2, 4 and 12 weeks and the specimens obtained were processed and analyzed histomorphometrically.

RESULTS: The depth and extent of peak bone necrosis were 124.509 µm and 2087.094 µm for the 1-min protocol, respectively, and 436.424 µm and 12046.426 µm for the 2-min protocol. Peak necrosis was observed in the second experimental week with both cryotherapy protocols.

CONCLUSIONS: The present results indicate that the 2-min protocol produced more marked bone necrosis than the 1-min protocol. Although our results cannot be entirely extrapolated to clinical practice, they contribute to the understanding of the behavior of bone tissue submitted to different cycles of liquid nitrogen freezing and may serve as a basis for new studies.

Key words: Cryosurgery. Osteonecrosis. Jaw diseases.

INTRODUCTION

The prefix "cryo" is derived from the Greek word "kryos", which means cold. Cryosurgery is a method that uses low temperatures for local tissue destruction⁴. The locally lethal effects of this method are the result of cell dehydration and the formation of intracellular ice crystal, causing direct cytotoxic injury and secondary vascular ischemia^11,12,13,25.

The maxillomandibular complex is prone to a variety of lesions that, although benign, might be locally aggressive^9,10,22,24. Doubts exist regarding the best therapeutic approach in these cases, since conservative management has been associated with high rates of recurrence, whereas radical treatment, although resulting in cure in most cases, may cause severe esthetic-functional impairment²¹. In this respect, adjuvant therapies, such as cryosurgery, have been combined with conservative modalities in order to reduce the rate of recurrence without increasing morbidity^5,21,23.

Animal models investigating the effects of cryosurgery on bone tissue have generally been used for descriptive purposes and have only evaluated morphological aspects^{3,7,8,14,15,19,20,27}. A broad review of the English-language literature revealed no standardized studies that histomorphometrically analyzed the effects of cryotherapy on bone tissue. The aim of the present study was to evaluate the effects of liquid nitrogen cryosurgery on the femoral diaphysis of rats using a standardized experimental model and histomorphometric parameters.

MATERIAL AND METHODS

Animals

Forty-two male Wistar rats aged 16 weeks (360-460 g), randomly chosen from the Central Animal House of the Federal University of Ceará, Fortaleza, CE, Brazil, were used in this study. The animals were housed in separate cages on a 12-24 h light/dark cycle at 23-25ºC, with free access to food and water. The experiments were reviewed by the Animal Care and Use Committee of the same institution (protocol number: 6/2006) and were conducted according to recommended guidelines on animal experimentation.

Cryosurgery protocols

Freezing was carried out in a CRY-AC^®-3 cryostat (model #B-700, Brymill, imported from CRY-AC^®, Brazil) using liquid nitrogen as coolant and a closed cryoprobe with a flat surface measuring 1 mm in diameter. The animals were divided into two groups according to the cryosurgery protocol used: group A was submitted to three 1-min freeze cycles intercalated with periods of 5 min of passive thawing, for a total freeze time of 3 min; group B was submitted to three 2-min freeze cycles intercalated with periods of 5 min of passive thawing, for a total freeze time of 6 min.

Surgical procedures

The rats were anesthetized by intraperitoneal injection of 2.5% tribromoethane (0.1 mg/100 g body weight). Next, a 1.5-cm linear incision was made along the lateral aspect of the right thigh from the proximal femur. The anterior thigh muscles were cut longitudinally and the femoral diaphysis was exposed. The joint ligaments were released and the tip of the closed probe was positioned on the bone surface 1 cm from the head of the femur. Retractors were carefully positioned to avoid damage to adjacent soft tissues during the freezing process. After cryosurgery, the muscles were returned to their initial position, and the soft tissues and skin were sutured. The animals were allowed to recover and were placed in individual cages. No drugs were administered postoperatively.

Histologic preparation

Groups of rats were sacrificed by cervical dislocation 1, 2, 4 and 12 weeks after surgery. The right femurs were removed, fixed by immersion in 10% neutral buffered formaldehyde for 48 h at room temperature, and then decalcified in 5% acid nitric for 10 days. After decalcification, the specimens were dehydrated in a graded ethanol series, placed in xylene, and embedded in paraffin in such a way that the femur could be sectioned in the sagittal plane. The site of cryoapplication was determined by positioning a millimeter rule 1 cm from the femoral head. Sections (4-µm-thick) were cut sequentially from the lateral border to the site of cryoapplication and stained with hematoxylin and eosin.

Histomorphometric analysis

For histomorphometric analysis, the data were processed using the Image J version software 1.43 s (National Institutes of Health, Bethesda, MD, USA; available from http://rsbweb.nih.gov/ij/). The most central stained section that corresponded to the site of cryoapplication was selected in each block. The sections were examined under a Leica DMLB light microscope (Leica Microsystems, Nussloch, Germany) connected to a Nikon Alphaphot-2 VS2 digital camera (Nikon, Tokyo, Japan). In each section, all histologic fields were analyzed and saved as digital images. The images were acquired using a 100x objective with a fixed grid and the following parameters were measured: (1) depth of bone necrosis, (2) extent of bone necrosis, (3) number of empty osteocyte lacunae, and (4) number of empty vessel channels. For depth and extent of bone necrosis, pixel values were converted into micrometers using a Neubauer chamber (0.1 mm/0.0025 mm²) at the same magnification. In addition, in each histologic field three vertical standardized measurements were made for the assessment of the extent of bone necrosis (Figure 1b), and a horizontal measurement was performed for the evaluation of the depth of bone necrosis (Figure 1d). Empty osteocytes and vessel channels are expressed as a numerical ratio, with the calculation of the proportion between empty and total lacunae ("empty" and "full") and between empty and total vessel channels (Figure 2a).

Statistical analysis

All measurements were made blindly, with the examiner being unaware whether the 1-min or 2-min protocol had been applied. Median, quartiles and minimum and maximum values were calculated for the variables studied. Statistical analysis was performed using the Origin 8.0 statistical program (Micronal Software, Northampton, MA, USA). The results were compared using the Kruskal-Wallis test and Dunn's post-hoc test was applied to groups in which more than two samples differed significantly. A level of significance of 5% was adopted (p<0.05).

RESULTS

One-minute protocol

The absolute peak extent of bone necrosis (2087.094 µm) was observed in the second week of the experiment. Comparison showed a significant difference (p<0.05) between experimental weeks, except between the first and fourth week. Pairwise comparison between weeks of observation showed a significant difference (p<0.05) in mean depth of bone necrosis per histologic field for most combinations, except between the first and second week. In addition, peak necrosis depth was 124.509 µm in the second week. A marked percentage of both empty osteocytes (Figure 2b) and vessel channels (Figure 2c) was observed in the second week, with mean ratios of 0.31 and 0.34, respectively.

Two-minute protocol

The peak extent of bone necrosis was 12046.426 µm and was observed in the second week of the experiment. A significant difference in necrosis extent was only observed between the first and second week (p<0.05) (Figure 1a). Regarding the depth of bone necrosis, a significant difference was observed between all weeks of this study (p<0.05) (Figure 1c). In addition, a mean depth of 436.424 µm was found in the second week. Necrosis of osteocytes (Figure 2b) and vessel channels (Figure 2c) was mainly observed in the second week, with mean ratios of 0.64 and 0.71, respectively.

DISCUSSION

In an attempt to reduce or even to prevent esthetic-functional complications associated with radical treatment of benign aggressive jaw diseases, alternative therapies such as the application of tissue fixatives (Carnoy solution) and cryogens (liquefied gauzes at a temperature below 0ºC) have been combined with conservative treatment^{1,17,21,23,26}.

On the basis of morphofunctional phylogenetic investigations¹⁸, we developed an experimental model using rat femurs for comparative studies in order to extrapolate the clinical use of cryotherapy to human jaw diseases. For standardization of the present method, a closed probe system was chosen since it permits better control of the quantity of tissue involved².

The present study is the first employing histomorphometric parameters for the evaluation of the tissue response to cryosurgery. The Image J software was used since it is a simple, public domain program freely available on the internet, which has also been used for other purposes in dentistry as reported by Demirbas⁶ (2008).

Analysis of the extent of osteonecrosis in animals submitted to the 1-min protocol showed no significant difference in mean values between histologic fields of animals evaluated after the same period of time. However, pairwise comparison of the different observation periods showed a significant difference between practically all periods, except between the first and fourth week. The highest mean total extent of necrosis was observed in the second week.

In contrast to the 1-min protocol, a significant difference in the mean extent of bone necrosis between histologic fields was observed in the second week for animals submitted to the 2-min protocol. Similarly, the highest mean extent of necrosis was observed in the second week compared to the other groups, but the difference was only significant when compared to the first week of observation.

Comparison of the protocols of liquid nitrogen cryosurgery showed a similar mean extent of necrosis between weeks, except for a significant difference between the second and 12^th week.

Another important parameter for the quantitative analysis of morphologic alterations resulting from cryotherapy is the percentage of necrotic osteocytes. Using the 1-min protocol, a significant difference in this parameter was observed in the second week when compared to the other weeks. The same was noted for the other experimental protocol. Comparison of the two protocols showed a significantly higher mean percentage of necrotic osteocytes for the 2-min protocol compared to the 1-min protocol, corresponding to peak osteocyte necrosis in the present study.

In addition to the quantification of osteocyte necrosis, significant differences in the devitalization of vessel channels were also observed between groups of the two protocols. As observed for the previous morphologic analysis, a significantly higher percentage of necrotic channels were noted in the second week of observation compared to the remaining weeks, with peak vascular necrosis also occurring in the second week as observed for osteocyte necrosis. In contrast, the lowest percentage of necrotic cortical vessels was observed in the last week of observation after cryotherapy, corresponding to peak vascularization in the present study.

The depth of necrosis in animals is generally evaluated by thermographic imaging, a procedure in which thermal needles connected to the target tissues monitor the local temperature field during the cryosurgical procedure¹⁴. Using this approach, Bradley and Fisher³ (1975) evaluated different methods of freezing bone in 2-cm wide surgical cavities of dry porcine mandibles. The authors observed that the use of nitrogen spray resulted in complete bone penetration, including the opposite cortex, after 5 min. In contrast, the use of closed probes resulted in a small area of cortical bone after 10 min where the cellular temperature reached a lethal level. However, these studies provided only immediate and in vitro results, whereas an in vivo longitudinal analysis using qualitative and quantitative parameters was performed in the present study.

We also observed differences in the depth of osteonecrosis between histologic fields, between weeks of observation and between the two cryosurgery protocols. Using the 1-min protocol, a significant difference in mean depth of bone necrosis between histologic fields was only observed in the group sacrificed after 1 week, with the observation of greater homogeneity in the band of necrotic cortical bone in the other groups. The highest mean necrosis depth was observed in the second week of evaluation, with this value being numerically similar to that obtained in the first week and significantly higher than those obtained in the remaining weeks using the same protocol.

In contrast to the 1-min protocol, when using the 2-min protocol, a difference in mean necrosis depth was observed not only for the one week group but also for the two week group. These groups also showed greater heterogeneity of the cellular effects of cryotherapy, with specific fields showing a greater necrosis depth. Mean necrosis depth was significantly higher in animals sacrificed after 2 weeks, similar to the findings obtained with the 1-min protocol.

In the present study, mean peak necrosis was significantly higher in the second week of observation using the 2-min liquid nitrogen cryotherapy protocol compared to the 1-min protocol. This finding agrees with Kuylenstierna¹⁵ (1980) who studied rabbit mandibles and observed marked bone necrosis in the second week of evaluation. In contrast, in a histologic study on rabbit femurs, Keijser¹⁴ (1999) demonstrated a clear demarcation of osteonecrosis one week after cryosurgery, similar to the findings obtained with the 1-min protocol of the present study.

Clinically, bone fractures after cryotherapy have mainly been reported for ameloblastoma involving the upper jaw bones, a benign but locally aggressive odontogenic tumor^{1,5,7,16,17,21}. Despite the absence of pathological fractures in the present study, we suggest that the marked bone necrosis observed especially in the second experimental week may contribute to the occurrence of this complication, a fact supporting the need for careful postoperative follow-up.

CONCLUSIONS

The findings of the present study indicate that the 2-min protocol produced more accentuated bone necrosis than the 1-min protocol. Although our results cannot be entirely extrapolated to clinical practice, they contribute to the understanding of the behavior of bone tissue submitted to different cycles of liquid nitrogen freezing and may serve as a basis for new studies. Experimental data are important for the understanding of the mechanisms underlying the effects of cryosurgery.

Received: September 24, 2009

Accepted: April 30, 2010

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Publication Dates

• Publication in this collection
  06 Mar 2012
• Date of issue
  Dec 2011

History

• Received
  24 Sept 2009
• Accepted
  30 Apr 2010