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Acta Cirurgica Brasileira

Print version ISSN 0102-8650

Acta Cir. Bras. vol.29 no.1 São Paulo Jan. 2014

http://dx.doi.org/10.1590/S0102-86502014000100002 

Original Articles

Cutaneous changes in rats induced by chronic skin exposure to ultraviolet radiation and organophosphate pesticide1

Tania Rita Moreno de Oliveira FernandesI 

Itamar SantosI 

Juliana Pedrosa KorinsfkyII 

Benedyto Sávio Lima e SilvaI 

Luis Otávio CarvalhoIII 

Hélio PlaplerIV 

IAssociate Professor, Department of Medicine, Federal University of Sao Francisco Valley (UNIVASF), Petrolina-PE, Brazil. Acquisition and interpretation of data

IIAssistant Professor, Nursing Department, UNIVASF, Petrolina-PE, Brazil. Intellectual and scientific content of the study, acquisition and interpretation of data

IIIFull Professor, Histology Division, Oswaldo Cruz Institute Foundation (FioCruz), Rio de Janeiro-RJ, Brazil. Histological analysis, interpretation of data, intellectual content of the study

IVAssociate Professor, Department of Surgery, Paulista Medical School (EPM), Sao Paulo Federal University (UNIFESP), Brazil. Conception, design, intellectual and scientific content of the study, critical revision

ABSTRACT

PURPOSE:

To study the possible potentiation of the carcinogenic effects of ultraviolet radiation associated with an organophosphate pesticide.

METHODS:

Forty Wistar rats were assigned into four groups (n=10 each) randomized according to the procedures: group A received only UVR-B radiation; group B, UVR-B for eight weeks followed by a seven week period of pesticide exposure; group C, UVR-B + pesticide concomitantly: group D, only pesticide application. At the end of the fifth, tenth and fifteenth weeks the animals were photographed. Skin biopsy and histopathological study with Hematoxylin-Eosin were done on the fifteenth week. Statistical analysis with Fisher's and Sign (unilateral) tests, 5% value for significance.

RESULTS:

Macroscopic lesions in the group A evolved from the erythema to erythema + desquamation. The groups B and C, with the association of two carcinogens, and group D presented evolution to keratosis, with higher incidence in group D. The histology showed a significant increase in the severity of injuries when the UVR-B and the pesticide were applied simultaneously, leading to cellular atypia.

CONCLUSIONS:

Concurrent association of UVR-B to organophosphate pesticide produced more severe lesions microscopically, although this has not been so apparent macroscopically. In daily practice the clinical evaluation should be complemented with laboratory evaluation.

Key words: Epidermis; Solar Radiation; Skin Neoplasms; Organophosphates; Rats

Introduction

Skin cancer (SC) is first place in prevalence in the world. According to the National Institute of Cancer (INCA), 134.00 of non-melanoma SC new cases were expected in Brazil in 2010, being the most frequent neoplasia in the Brazilian population for both genders, representing approximately 25% of the total number of new cases of cancer1.

The American Cancer Society estimated that, in 2007, more than one million cases of non-melanoma skin cancer (NMSC) - basal cells carcinoma (BCC) and spinocellular carcinoma (SCC) - and about 60.000 cases of melanoma (CM) would be associated to ultraviolet radiation (UVR)1.

Carcinogenesis begins when the DNA of a cell is damaged by the exposure to mutagenic endogenous and/or exogenous substances during cell division, resulting in mutations, chromosomal translocations, deletions, inversions or gene amplification. The promoting stage of the tumor is characterized by successive clonal expansion of tumor cells, and the genetic alterations and environment factors, such as the exposure to ultraviolet radiation (UVR) and to cancerous substances, are responsible for the majority of cancer cases2 - 6. Pesticides induce cancer through various mechanisms, such as gentoxicity and tumor promotion involving hormonal, immunological mediators and the production of oxidant molecules peroxide8.Its absorption through the skin varies according to room temperature (bigger in high temperatures), air humidity, contact time with the skin and carcinogenic potential. Studies about toxicity of pesticides use a 50% dermic lethal dose (LD-50 dermic)9.

Petrolina and Juazeiro are neighbor cities, with the biggest urban population in the Brazilian semi-arid climate region, approximately 530.747 people10, corresponding to 50% of the economically active population11. In order to make the agricultural economy possible, the pesticides are used indiscriminately. According to Bedor9, the most used pesticides in the region belong to the following groups: organophosphate s (25%), piretodes (9%), benzimidazole and triazole (6%), neocotinodes (5%).

Among the organophosphates, Folisuper(r) (parationa- metílica): O,O- dimethyl O- 4- nitrophenylphosphorothioate (molecular formula C8H10NO5PS) is the most used one, classified as extremely toxic. It has been considered in many pre carcinogenic studies as being very dangerous to the environment9. Organophosphates are highly soluble in lipids and they can be absorbed by the skin, either by ingestion or inhalation.

Solar radiation in known as a carcinogenic factor and pesticides are co-carcinogenic to the human body and has the skin as one of its main ways of absorption. This study aims at evaluate a causal link between this association and SC.

Methods

This project was approved by the Animal Experimentation Ethic Committee of São Paulo Federal University (protocol number 1146/10) and Scientific Research Ethic Committee at the Sao Francisco Valley University (protocol nº 12081048).

This is an animal model aligned to a follow-up study, using forty 3-month-old, male Wistar rats (Rattus norvegicus albinus), with average weight of 250±30g proceeding from the laboratory animal center.

All animals were shaved leaving a bald dorsal area measuring 3x3cm every seven days, with an electrical shaver and then were randomly assigned into four groups, called A, B, C and D. The observation time was 15 weeks (from 05/07/2010 to 17/10/2010). This time interval was determined by the arithmetical average of observation time used by Fisher et al.11, Mitchell et al.12, Kligman et al. 13, Schwartz14 , 15and Wulff et al.16.

Group A (n=10) had UVR-B applied to the animals skin. Group B (n=10) had its animals exposed to UVR-B for eight weeks, then associated to a seven week period when a layer of pesticide was also applied. In group C (n=10), the skin of the animals was exposed to UVR-B followed by a layer of pesticide alone. In group D (n=10), only a layer of pesticide was applied.

Procedures

Pesticide application

A solution of "Folisuper(r)" (C8H10NO5PS) diluted in distilled water 0,4mg/kg (according to the product label directions) was applied topically on the shaved dorsal skin of the animals three times a week for 15 weeks through a wooden stamp with foam on its extremity.

Ultraviolet radiation (UVR-B)

A UVR emitter device was used for stable wave lengths (λ) of 312nm (type B) Spectroline(r) ENB-260 C-Dual Wavelength E series and power of 6J/s (W) and 1,7A Long wave (UVA 365nm)/Medium wave (UVB 312nm) (Espectronic Co. St. Westberry, Ny, USA), In order to use this device, a wooden rectangular box was confectioned to keep the animal immobilized while submitted to radiation, 20cm away from the UVR -B emitter device. The animals from groups A, B and C were exposed for 30 seconds three times a week15 , 16. Exposure time was based on the lamp potency and minimum time necessary to obtain twice as much the erythematous dose on the animal skin.

Photograph analysis

Pictures were taken at the end of the fifth, tenth and fifteenth weeks and analyzed blindly by an experienced dermatologist according to the following score: no lesion, physical scar, erythema, erythema with desquamation, keratosis, ulcer, crust and vegetation.

Biopsy procedures and histologic analysis

After identification, skin fragments were sent for histological analysis in a 10% formaldehyde solution, to FioCruz Laboratory in Rio de Janeiro and stained by the Hemathoxylin-Eosin method. They were photographed, being prioritized the sites with more pathological findings (10 and 20 fold objective). A high resolution video camera (AxionCam MRC, Carl Zeiss(r), Jena, German) was attached to the microscope.

Histological analysis

The analysis took place at the Histotec Pathology Laboratory, located in Petrolina-PE, by a pathologist using a Nikon microscope model Elipse E 200 with binocular lenses with enlargement of 10x and objective with enlargement x40/0.65 attached to the video camera. To the microscopic analysis the following alterations were considered2 , 3 , 17:

Acanthosis: thickening of the spinous layer due to the increase in the number and size of cells.

Hyperkeratosis: thickening of the horny layer of the epidermis, infundibulum or eccrine/apocrine ducts.

Epithelial dysplasia: atypical and irregular proliferative response to chronic irritation, reversible, characterized by the increase in proliferation associated to the presence of atypical cells, involving alterations in cell size, number and organization.

Cellular atypia: changes in size and shape of the cell, nucleus and nucleolus; disproportion of the nuclear and cytoplasmic presence of abnormal mitoses.

Statistical analysis

Macroscopic: a descriptive analysis of the variables has been carried out using the exact test performed by Fisher and the Signal test (unilateral).

Microscopic: the distributions of the frequency of variables were compared in the four groups by the exact test of Fisher. In all comparisons the probabilities lower than 0.05 were taken into consideration.

Results

The results of this study are presented in the following tables and pictures.

Macroscopic analysis

Tables 1 to 3 display the distribution of the skin lesions and Figures 1 to 4 exemplify them.

TABLE 1  Perceptual distribution of the studied variables (mode) at fifth week. 

Statistic variable Groups Comparison
A B C D between groups
value - p Conclusion at 5%
Number of rats 10 10 10 10
Fisher´s test
Frequency 0.698 accepted H0
Nº lesion (n) 10% (1) 0% (0) 10% (1) 0% (0)
Physical excoriation (n) 0% (0) 0% (0) 10% (1) 10% (1)
Erythema (n) 40% (4) 30% (3) 40% (4) 30% (3)
Erythema with Dequamation (n) 20% (2) 40% (4) 10% (1) 10% (1)
Keratosis (n) 30% (3) 20% (2) 30% (3) 50% (5)
Ulcer (n) 0% (0) 0% (0) 0% (0) 0% (0)
Crust (n) 0% (0) 10% (1) 0% (0) 0% (0)
Vegetation (n) 0% (0) 0% (0) 0% (0) 0% (0)
Total 100% (10) 100% (10) 100% (10) 100% (10)

TABLE 2  Perceptual distribution of the studied variables (mode) at tenth week. 

Statistic variable Groups Comparison between groups
A B C D value - p Conclusion at 5%
Number of rats 10 10 10 10
Fisher´s test
Frequency 0.744 accepted H0
Nº lesion (n) 0% (0) 0% (0) 0% (0) 0% (0)
Physicalexcoriation (n) 0% (0) 0% (0) 0% (0) 0% (0)
erythema (n) 30% (3) 30% (3) 30% (3) 20% (2)
Erythema / dequamation (n) 50% (5) 40% (4) 20% (2) 30% (3)
Keratosis (n) 20% (2) 30% (3) 50% (5) 50% (5)
Ulcer (n) 0% (0) 0% (0) 0% (0) 0% (0)
Crust (n) 0% (0) 0% (0) 0% (0) 0% (0)
Vegetation (n) 0% (0) 0% (0) 0% (0) 0% (0)
Total 100% (10) 100% (10) 100% (10) 100% (10)

TABLE 3  Perceptual distribution of the studied variables (mode) at fifteenth week. 

Statistic variable Groups Comparison between groups
A B C D Value-p Conclusion at 5%
Number of rats 10 10 10 10
Fisher´s test
frequency 0.222 accepted H0
Nº lesion (n) 10% (1) 0% (0) 10% (1) 0% (0)
Physical excoriation (n) 0% (0) 0% (0) 10% (1) 0% (0)
Erythema (n) 0% (0) 20% (2) 20% (2) 10% (1)
Erythema / dequamation (n) 60% (6) 20% (2) 20% (2) 10% (1)
Keratosis (n) 30% (3) 60% (6) 40% (4) 80% (8)
Ulcer (n) 0% (0) 0% (0) 0% (0) 0% (0)
Crust (n) 0% (0) 0% (0) 0% (0) 0% (0)
Vegetation (n) 0% (0) 0% (0) 0% (0) 0% (0)
Total 100% (10) 100% (10) 100% (10) 100% (10)

FIGURE 1  Group A: keratosis and erythema. 

FIGURE 2  Group B: advanced keratosis, erythema and scars. 

FIGURE 3  Group C: keratosis, erythema and scars. 

FIGURE 4  Group D: intense keratosis, erythema. 

Histological findings

Among the alterations found as representative for the purpose of this study, we chose the following variables: acanthosis, hyperkeratosis, dysplasia and cell atypia (Table 4).

TABLE 4  Percentage distribution (frequency) of the histological variables presented by the groups. 

Variables Groups
A B C D
Acanthosis
light (n) 80% (8) 10% (1) 90% (9) 50% (4)
mild (n) 20% (2) 80% (8) 10% (1) 25% (2)
srtong (n) 0% (0) 10% (1) 0% (0) 25% (2)
total 100% (10) 100% (10) 100% (10) 100% (8)
Hyperkeratosis
light (n) 90% (9) 100% (10) 10% (1) 87.5% (7)
mild (n) 10% (1) 0% (0) 10% (1) 12.5% (1)
srtong (n) 0% (0) 0% (0) 80% (8) 0% (0)
total 100% (10) 100% (10) 100% (10) 100% (8)
Dysplasia
light (n) 100% (10) 0% (0) 10% (1) 0% (0)
mild (n) 0% (0) 90% (9) 80% (8) 62.5% (5)
srtong (n) 0% (0) 10% (1) 10% (1) 37.5% (3)
total 100% (10) 100% (10) 100% (10) 100% (8)
Cell atypia
present (n) 100% (10) 10% (1) 0% (0) 62.5% (5)
absent (n) 0% (0) 90% (9) 100% (10) 37.5% (3)
total 100% (10) 100% (10) 100% (10) 100% (8)

Figures 5 to 8 display the histological findings listed in Table 4.

FIGURE 5  Group A: mild dysplasia, acanthosis and dermic edema. 

FIGURE 6  Group B: hyperkeratosis, diskeratosis, atipic cells and dysplasia. 

FIGURE 7  Group C: atipic cells, hyperkeratosis, diskeratosis and dysplasia. 

FIGURE 8  Group D: atipic cells, dysplasia, superior dermic edema and diskeratosis. 

Discussion

UVR is proved to be carcinogenic, acting directly on the cellular DNA and causing cutaneous immunosuppression, mainly through its UVR-B band, being the main etiological factor of the main SC1 - 5 , 18 - 20. Experimental research using animal models (rats, mice) has shown the association between the exposure to UVR and SC17 , 19 - 23. The association between pesticides and cancer has already been well demonstrated8 , 9 , 24 , 26 and some studies cover the association between pesticides and SC2 , 24 - 26; however, there are very little studies showing the association between UVR, pesticides and SC in animal models27. Clinical and experimental studies have not explained the mechanisms of these alterations yet11 , 12 , 27.

The cutaneous alterations which occur after chronic solar exposure, such as pigmentation, immunosuppression, keratosis and SC, are related to the wave length and to the total UVR dose that act on the individual susceptibility2 , 3 , 5.

According to Honda22 and other authors, the chronic exposure to UVR may increase the occurrence of mutations on p53 gene, causing a deregulation in the apoptosis pathway and start SC. According to Matsumara4, at the molecular level, UVR damages the DNA to pyridimine dimmers and photoproducts, which are normally repaired through excision repair system, and affirms that photocarcinogenesis involves the buildup of genetic alterations as well as the immune system modulation and finally causes the development of SC.

According to Roewert-Huber et al.27, the dermatological elementary lesion caused by the sun rays are initially seen as erythema, then as desquamation and finally as scars forming an actinic keratosis, followed by the formation of a crust and even the evolution to SCC27.

This study shows (time 1), in the group of animals exposed to UVR-B (Group A), a higher prevalence of erythema (Figure 1). As the exposure goes on (times 2 and 3), it gets to the following evolution step (erythema + desquamation) (Table 1), which can be considered as the first step in the formation of actinic keratitis (AK). It is likely that this is due to the expected action of UVR-B that happens every time the exposure goes over the tolerance limit. They happen as a consequence of a pericapillar aromatic protein oxidation process. This molecular alteration causes protaglandins liberation and also the release of other vasodilation substances through mastocytes degranulation and through the release of erytrogenic substances as a consequence of the lesion of keratinocytes and leukocytes2 , 3 , 5. To the development of SCC and BBC, the correlation between the UVR absorption and the start of cutaneous neoplasia are conclusive although questionable in melanoma2 - 4. Honda et al.22 managed to develop SC in mice which were exposed to chronic UVR-B after 14 weeks. Wulff et al. 16 tested the effect of celecobrix to determine the effects of anti-inflammatory treatment associated to immunosuppression in the development of SC previously initiated and promoted by using mice which were exposed to UVR-B three times a week for 15 weeks to induce the development of SC.

In the groups of animals exposed simultaneously to UVR+AGRO (B and C), it is possible to see alterations which start with erythema and progress to keratosis as the histologic study reveals (Figures 2 and 3). Many authors, after the exposure of the mice and rats to UVR, concluded that the cutaneous carcinomas appear depending on the radiation dose. The latency period is additionally influenced by the radiosensibility genetically determined (quantity of melanin in the skin and DNA repair) and by the action of sincarcinogenic and concarcinogenic factors (including pesticides). Wang et al.18 induced SC in mice by using UVR-B and UVR-A associated to benzopyrene. Gallagher et al.25 associated plasmatic levels of polichloridebifeniles (organchloride), sun and the risks of CM.

In the group of animals exposed only to the pesticide, the predominant cutaneous alterations were keratosis (Figure 4) with an expressive level of erythema and erythema + desquamation. This evidence is in accordance with information from Oregon State University in its Extonet archives8: "a quantity of pesticide absorbed by the SCis sufficient to produce toxic reactions including death, skin irritation and cutaneous eruption or inflammation and its level is a direct result of the level of chemical or physical irritation (dose-response)". Still, according to the archive, the organophosphate in this study is the cause of allergic contact dermatitis, which is clinically seen as erythema, inflammation and in a later stage, skin thickening8. The formation of keratosis predominantly in the pesticide group (D) in this study can indicate initial neoplastic lesions (AK).

According to Roewert-Huber et al.27, microscopically, in the initial phase of the induced aggression by UV rays, hyperkeratosis and acanthosis happen27 (Table 2) and are in accordance with the findings of this study for all groups. The acathosis is determined both by the aggression UVR-induced and by the irritative action of the pesticide8.

As for the hyperkeratosis, the expected effected of the UVR action could be observed in groups A and B, the same way as it was found by Popim2 and Roewert-Huber et al.27, being part of the histologic alterations that suggest the diagnosis for AK2 , 3 , 5 , 18 , 27.

For group C, the action of UVR with the pesticide together resulted in the development of the hyperkeratosis more heavily, which possibly means an inducting action to precancerous lesions26.

For group D (pesticide) there is an absolute predominance of the light form of hyperkeratosis, which suggests the irritant effect (contact dermatitis) of this substance8.

Regarding to dysplasia, we can see that group A showed only mild dysplasia (Figure 5), the expected action of UVR alone19. Wang et al. 26found skin tumors in mice irradiated with UV rays associated with benzopyrene for 30 weeks. Further studies using a longer exposure time will be needed to observe the evolution of skin lesions caused by UVR association.

The microscopic findings in this study suggest that the lesions characterize the diagnosis of actinic keratosis, which was more severe in groups which had the association between the pesticide and UVR-B, including a higher level of dysplasia.

Actinic keratosis is considered as cutaneous neoplasia with chromosomal abnormalities, which is consequence of the long solar exposure, but can also be due to the exposure to radiations from artificial sources and aromatic hydrocarbons2. Histologically, it is seen mainly as an epidermal thickening associated to various levels of dysplasia, which varies from small alterations to carcinoma in situ. The most frequent type of solar keratosis presents acanthosis and hyperkeratosis27. The AK is different from the SCC due to the absence of inversion of the dermis18 , 26. Epithelial dysplasia is constant and consists of loss of maturation, abnormal cell polarity, nuclear and cytoplasmic pleomorphism, keratinization of individual cells and mitotic figures abnormally located26 , 27.

The cutaneous alterations caused by the ultraviolet radiation have already been demonstrated, as well as the carcinogenic potential of pesticides to the organism as a whole. In the daily dermatological practice, the clinical evaluation must be complemented by the laboratory evaluation. Histological findings in this study characterize the diagnosis of actinic keratosis for UVR, UVR + AGRO and AGRO, more pronounced where there was association between UVR-B and the pesticide, since dysplasia was present in a higher degree.

Conclusions

Concurrent association of UVR-B to organophosphate pesticide produced more severe lesions microscopically, although this has not been so apparent macroscopically. In daily practice the clinical evaluation should be complemented with laboratory evaluation. Histological evaluation is more reliable than the clinical evaluation to define the type of lesion inducted by UVR either or not associated to pesticides.

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1 Research performed at Laboratory of Experimental Surgery, Sao Francisco Valley University (UNIVASF), Petrolina-PE, Brazil. Part of Master degree thesis, Postgraduate Program in Interdisciplinary Surgical Science, Sao Paulo Federal University. Tutor: Helio Plapler.

Received: September 17, 2013; Revised: November 18, 2013; Accepted: December 20, 2013

Correspondence: Tania Rita Moreno de Oliveira Fernandes Disciplina de Técnica Operatória e Cirurgia Experimental Rua Botucatu, 740 04023-900 São Paulo - SP Brasil trmofernandes@gmail.com

Conflict of interest: none

Financial source: none

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