Changes in the volume and histology of endometriosis foci in rats treated with copaiba oil (Copaiferalangsdorffii)

Mudanças no volume e histologia do foco de endometriose em ratas tratadas com óleo de Copaíba (Copaiferalangsdorffii)

5 - ORIGINAL ARTICLE MODELS, BIOLOGICAL

Changes in the volume and histology of endometriosis foci in rats treated with copaiba oil (Copaiferalangsdorffii)¹

Mudanças no volume e histologia do foco de endometriose em ratas tratadas com óleo de Copaíba (Copaiferalangsdorffii)

João Nogueira Neto^I; Márcio Jorge de Souza Lindoso^II; Laura Fernandes Coelho^II; Rafael Antonio Freire Carvalho^II; Taciana Gabrielle Pinheiro de Moura Rodrigues^II; Ana Gisélia Portela de Araújo^III; Manuel João Batista Castelo Girão^IV; Eduardo Schor^V

^IMD, Fellow PhD degree, Federal University of Sao Paulo (UNIFESP), Unit of Endometriosis of HU-UFMA, Brazil. Design the protocol, involved with technical procedures, responsible for manuscript writing, responsible for intellectual and scientific content of the study, supervised all phases of the study, and provided guidelines for the surgical interventions

^IIGraduate student, UFMA, Maranhao, Brazil. Involved with technical procedures, responsible for manuscript preparation

^IIIMD, HUUFMA, Maranhao, Brazil. Macroscopic and histopathological examinations

^IVPhD, Department of Ginecology, Paulista School of Medicine, Federal University of Sao Paulo (EPM-UNIFESP), Brazil. Responsible for intellectual and scientific content of the study, critical revision, provide guidelines for the surgical interventions

^VPhD, Affiliate Professor, UNIFESP, Head of Unit of Pelvic Pain and Endometriosis, EPM-UNIFESP, Sao Paulo, Brazil. Responsible for acquisition and interpretation of data, statistical analysis, helped with technical procedures, collection and processing of study informations, provide guidelines for the surgical interventions

^{Correspondence}

ABSTRACT

PURPOSE: The aim of this study was to analyze the changes that occur in rats with experimental endometriosis after treatment with copaiba oil.

METHODS: Experimental endometriosis was induced in rats. The experimental group received copaiba oil (Copaiferalangsdorffii) orally (0.63 mg/day), and the control group received a 0.9% sodium chloride solution orally (1 ml/100 g of body weight/day). Both groups were treated with gavage for 14 days. After this period, the animals were euthanized, and the implant volume was calculated. The autologous transplants were removed, dyed with hematoxylin-eosin, and analyzed by light microscopy.

RESULTS: The average final volumes were significantly different between the groups (p=0.007). There was a significant increase (p=0.012) between the initial and final volumes in the control group, whereas treatment with Copaiferalangsdorffii caused a marked reduction in endometrial growth over time (p=0.016). Histologically, 6/11 (55.00%) rats in the experimental group had a well-preserved epithelial layer, and 3 (45.00%) had mildly preserved epithelium. The control group had seven cases (58.30%) of well-preserved epithelial cells and five cases (41.70%) of mildly preserved epithelial cells (p>0.05).

CONCLUSION: Copaiba oil (Copaiferalangsdorffii) appears to be a promising alternative treatment for endometriosis.

Key words: Phytotherapy. Endometriosis. Drug Therapy. Rats.

RESUMO

OBJETIVO: O objetivo deste estudo foi analisar as mudanças que ocorreram em ratas com endometrioses experimental tratadas com óleo de copaíba.

MÉTODOS: Foi induzida a endometriose experimental nas ratas. O grupo experimental recebeu óleo de copaíba (Copaiferalangsdorffii) oralmente (0,63mg/dia) e o grupo controle recebeu oralmente solução salina 0,9% (1mL/100g/dia). Ambos grupos foram tratados por gavagem por 14 dias. Depois desse período, foi realizada a eutanásia dos animais e calculado o volume do implante. Os transplantes autólogos foram removidos, corados com Hematoxilina-eosina e realizada a microscopia óptica.

RESULTADOS: A média final dos volumes foi significativamente diferente entre os grupos (p=0,007). Houve um aumente significante (p=0,12) entre o volume inicial e final do grupo controle, enquanto no grupo tratado com Copaiferalangsdorffii causou uma redução acentuada no crescimento endometrial ao longo durante o período (p=0,016). Histologicamente,6 das 11 (55%) ratas do grupo experimental tinha uma camada epitelial bem preservada e 3 (45%) apresentaram epitélio levemente preservado. O grupo controle apresentou sete casos (58,3%) de células epiteliais bem preservadas e cinco casos (41,7%) de células epiteliais levemente preservadas (p>0,05).

CONCLUSÃO: O óleo de copaíba (Copaiferalangsdorffii) parece ser um tratamento alternativo promissor para endometriose.

Descritores: Fitoterapia. Endometriose. Quimioterapia. Ratos.

Introduction

Endometriosis is a condition that affects 10% of women, and often causing pelvic pain and infertility. Diagnosis is sometimes difficult and the optimal treatment is yet to come. Some events of the pathophysiology of endometriosis are well known, such as inflammation, immunomodulatory disorders, increased local and systemic oxidative stress, among others. The search for new treatments for endometriosis is justified when interfering in the events mentioned above¹.

The copaibas are trees in the Leguminosae-Caesalpinoideae family, reaching 25-40 feet tall and can live upto 400 years. Copaiba oil, in biological terms, is a product of excretion or detoxification of the plant organism, and acts as a plant defence against animals, fungi and bacteria². The attributed effects to Copaiba oils in folk medicine are anti-inflammatory, anti-tumour, anti-tetanus, anti-blenorrhagea, as a urinary anti-septic, to treat bronchitis, syphilis, skin diseases, ulcers, as well as for healing wounds³.

Some properties of Copaiba oil are well documented in the scientific world, which could justify its use in the treatment of endometriosis. Its anti-inflammatory effect had been observed in the research, which used kaurenoico acid, extracted from Coapiferalangsdorffii, and used in Wistar rats with induced colitis. Furthermore, light microscopy revealed the marked reduction of inflammatory cell infiltration and submucosal oedema formation in the colon segments of rats treated with the test compound⁴. The anti-inflammatory activity was confirmed in a comparative study between oils from Copaiferacearensis, Copaifera reticulate and Copaiferamultijuga in vitro and in vivo⁵. The study indicated that Copaiba oils demonstrate peripheral and central antinociceptive effect and may be useful in the treatment of algesic disorders⁶.

Another study examined the effects of Copaiferalangsdorffii resin on intestinal damage associated with mesenteric ischemia/reperfusion (I/R) in rats. Caused significant attenuations in I/R - associated increases of myeloperoxidase, malondialdehyde, catalytic activities and nitrite level. Copaiferalangsdorffii could effectively prevent the I/R-associated depletion of glutathione. The data indicate that the copaiba provided protection against I/R-induced intestinal tissue damage, which appeared to be, at least in part, due to an antioxidant and anti-lipid peroxidation mechanism⁷.

Antimicrobial activity was revealed through disruption and damage to the cell wall, resulting in the release of cytoplasmic compounds, alterations in morphology, and a decrease in cell volume, indicating that copaiba oil may affect the cell wall. Another effect that suggests anti-cell-proliferation was shown in a study that showed significant activity against the parasite Leishmania amazonensis ⁸.

The development of experimental endometriosis in female rats through auto-transplantation techniques prompted research on additional medical treatments for endometriosis. These treatments were analyzed for their efficacy via macroscopic and histological parameters, among others^9,10.

Because of the known properties of Copaiferalangsdorffii and its relationship to mechanisms involved in the etiopathogeny of endometriosis, the present study aimed to analyze its effects on experimental endometriosis implants in rats.

Methods

The study was carried out between March and Julyof 2010, using 40 60-day-old (adult) female Wistar rats (Rattus norvegicus albinus), weighing 180-250g. The rats were obtained from the bioterium of the Federal University of Maranhao (UFMA).

The study was developed in the Experimental Surgery Laboratory of the University Hospital of UFMA, Brazil. Study procedures followed the regulations of the Brazilian Legislation for the use of experimental animals (Arouca Act n° 11.794 /2008) and of the Brazilian Animal Experimentation College (COBEA), an institution affiliated with the International Council for Laboratory Animal Science. The study was approved by the Animal Experimentation Ethics Committee (CEEA-UEMA) under protocol number 035/2010.

The animals were grouped four per polypropylene cage (46 cm x 31 cm x 16 cm) with a stainless steel grid lid and a paper covered floor that was replaced every 48 hours. The animals were divided into four groups and maintained under constant environmental conditions. These including rat rations (PURINA^®, São Paulo, Brazil) and water ad libitum for seven days for adaptation; noise control; 22°C ± 2°C temperature; 40% to 60% relative humidity; and 12/12 hour light/dark cycles.

The autotransplantation technique was performed according to the methodology proposed by Nogueira et al.¹. Shortly after the midway incision, the uterine horns were identified; fragments of the medium third were resected, immersed in saline solution and cut into 4mm by 4mm fragments. The fragments were sutured to the mesentery adjacent to the artery that irrigates the cecum, with the serosa faces turned to the peritoneum and the endometrial layer turned to the cavity (Figure 1).

After the first surgery, the animals were kept in the lab for a period of 21 days. Following this period, the rats underwent an additional operation. An inventory of the peritoneal cavity was taken using a digital pachymeter to identify the success of the autotransplantation, followed by a volume calculation using the following formula: [4 (lenght/2)x(width/2)x(hight/2)/3]¹¹. Classification of the experimental endometriosis implant growth was performed⁹, and only those animals that progressed to a growth score of III remained in the study (Figure 2).

After the surgical approach, the rats were identified and randomly divided into the Copaiferalangsdorffii (COP group) and the control group (C group), both containing 12 rats.

The COP group gavaged oil (Óleo de Copaiba^® All Chemistry, lot 34883, São Paulo, Brazil) at 0.63mg/day for 14 days was carried out for Brito et al. in 2000¹². The C group received 1 ml daily gavage of 0.9% saline solution for 14 days.

After the end of the medical treatments, the rats were anesthetised using ketamine, and a third laparotomy was performed.

After opening the abdominal wall, an inventory of the peritoneal cavity and measurements of autotransplant volumes were performed; the transplant and the middle third of the uterine horn remaining were then removed. The salvaged tissue was rinsed with 0.9% saline solution and stored in 10% formaldehyde buffer for later anatomopathological analysis.

Paraffin tissues were sectioned in 5µm widths and placed in a warm bath; the slides were incubated with Meyer albumin and dried afterwards. Tissue sections were stained with hematoxylin-eosin (HE), and a histological analysis was performed by a pathologist. The oestrous cycles were analyzed in the middle third of the uterine horn remaining and drug efficacy was evaluated¹⁰. The persistence of epithelial cells in uterine autografts was evaluated as follows: a well-preserved epithelial layer = score 3, a moderately-preserved epithelium with leukocyte infiltrate = score 2, a poorly-preserved epithelium (occasional epithelial cell only) = score 1, and no epithelium = score 0 (Figure 3).

Biostat 3.0 Windows XP was used for statistical analysis, where the significance level () used to reject the null hypothesis was 5% (p<0.05). The Mann-Whitney test was used for independent samplings, and the Wicoxon test was performed for related samples. Fisher's exact test was used to analyze the histopathologic score.

Results

Initially there were 12 samples in each group. Due to technical problems, one sample of the experimental group was lost. This left 11 samples in the experimental group. All of the middle third of the uterine horn remaining was in either the proestrus or oestrus phase of oestrous cycle.

There was no significant difference between the mean volume (38.09 mm³) in the C group and (47.00mm³) that in the COP group at 21 days following the induction of endometriosis (p=0.470). Two weeks after administering copaiba oil and saline solution, the final average volumes were 65.40mm³ for the C group and 23.38mm³ for the COP group (p=0.007).

Average volumes for the initial control group and the saline-treated group two weeks later were 38.09mm³ and 65.70mm³, respectively. This increase in average volume was significantly different (p=0.012). For the COP group, the initial average volume was 47.00mm³, in contrast to the 23.38mm³ final average, and these measurements were also significant (p=0.016) (Table 1).

Regarding preservation of the epithelial layer, upon histological evaluation of the autotransplant focus the experimental group (n=11) contained six cases (55.00%) with a well-preserved epithelial layers (Figure 2), and five cases (45.00%) with mildly-preserved epitheliums. The control group (n=12) included seven cases (58.30%) with well-preserved epithelial cells and five cases (41.70%) of mildly-preserved epithelial cells. No significant differences were presented (p>0.05).

Discussion

The treatment of endometriosis is either clinical or surgical or both. The drugs commonly used interfere with the menstrual cycle, and after the drug taking is suspended, there is a reoccurrence of the pathology. Although the surgeries can be simple, they are often mutilating. It is important to do the experimental tests with therapeutic options that go against what has happened in pathogenesis of endometriosis, mainly in the interference of the inflammatory process and oxidative stress¹.

The copaiba oil is extracted from trees of the species Copaifera, popularly known as "copaiba", "copaíva" or "pau-de-óleo". It is known to have the following medicinal qualities: anti-inflammatory; anti-tumoral against Walker sarcoma and melanoma cell line; anti-ulcerogenic, antioxidant and anti-lipoperoxidative; cercaricide and anti- helmintic; insect repellent and antimicrobial. The cosmetic industry uses copaiba oil in shampoos, capillary lotion and bathing foams⁶.

The copaiba oil used in this research was extracted from the species Copaiferalangsdorffii, which has scientifically confirmed anti-inflammatory and antioxidant effects^4,7, justifying its experimental use in endometriosis.

The doses used in this research were based on studies that used the copaiba oil in different doses (0.63 ml/kg and 0.06 ml/kg during 14 days), followed by microscopic hepatic evaluation of the rats, in which no hepatocelular alteration was found. The volume used in the pilot plan was 1.26 ml/kg during 14 days, where on the 5^th day 90 % of the samples died. The volume was fractioned to 0.98 ml/kg ((3/4 de 1.26 ml/kg), 0.63 ml/kg (¹/₂ of 1.26 ml/kg) and 0.31 ml//kg ¼ de 1, 26 ml/kg). This way, the doses of 0.63 ml/kg was standardized, representing the highest volume from which there were no mortalities in the period of 14 days, and considered sufficient to realize the major part of the experiment that used copaiba oil¹². Our research reassured the security of the mentioned doses as there were no mortalities in our study.

Statins represent a class of drugs that can effectively decrease the serum level of cholesterol and is largely used in the treatment of hypercholesterolemia. Experimental studies show that these drugs effectively decreased the inflammatory processes and are anti-oxidant, and so were used in endometriosis experiments with similar methodology employed in this research. The sinvastatin used in the dose of 20 mg/kg/day during 14 days showed a significant regression of the focus of autotransplants when comparing the final volumes between the experimental and the control group¹. Studies that used atorvastatin in high doses showed similar results¹³; results that are compatible with our research on copaiba oil.

Melatonin is the product of the secretion of the pineal gland whose main function is regulating sleep, but also has anti-inflammatory, antioxidant and immunomodulator properties. It was used in an experimental endometriosis rat model treated with melatonin (10 mg/kg) intraperitoneally, with the evaluation of the morphology of the autotransplants, the expression of COX-2 and antioxidants enzymes. After four weeks of treatment it showed significant reduction of the autotransplant volumes, COX-2 and antioxidant activities in the experimental group¹⁴. The morphological evaluation with the significant reduction in volume agreed with our results.

Strong evidence of the anti-inflammatory effect in the reduction of the volume of the focus of the autotransplants in rat model endometriosis is proven in studies that use dexametason (0.8 mg/kg/day) for 13 days in Wistar rats. The dexametason significantly reduced inflammatory processes, the amount of collagen in the stroma, and the area occupied by the glands of the autotransplants¹⁵.

The histological evaluation didn't show compatible alterations with what was seen macroscopically without significant alterations. The use of melatonin showed significant histological changes in the experimental group when compared to the control group, but the author himself criticizes this type of evaluation because it is semi quantitative¹⁴.

The similar volume reduction of the copaiba oil when compared to anti-inflammatory, anti-oxidants and even imunommodulators confirmed the theoretical suspicion of the possible action against the development of focus of experimental endometriosis and opens one more possible line of research for the treatment of endometriosis.

Conclusion

The copaiba oil, at least of the species Copaiferalangsdorfii, seems to be a promising therapeutic option in the clinical treatment of endometriosis.

Correspondence:

João Nogueira Neto

Av. dos Holandeses S/N Qd 24 Lote 05/901

65071-380 São Luís - MA Brasil

[e-mail]

Conflict of interest: none

Financial source: none

Presented at the XII National Congress on Experimental Surgery of the Brazilian Society for Development of Research in Surgery-SOBRADPEC, 2011 October 26-29 Ribeirao Preto-SP, Brazil.

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Research performed at Experimental Surgery Laboratory, University Hospital, Federal University of Maranhao (LACEMA-HUUFMA), Brazil.

Publication Dates

• Publication in this collection
  24 Oct 2011
• Date of issue
  2011