Formaldehyde is a chemical which is traditionally used for fixing cadavers and routine histopathology techniques. It is vaponsed during the dissection and practical study of a cadaver. Previous studies have shown that this vapour may cause clinical symptoms such as throat, eye, skin and nasal irritation. This study was designed to determine the histopathology and morphometrics of the rat testis when all the experimental animals were exposed to formaldehyde for 18 weeks. The study was performed in 2004 on 28 albino Wistar rats of 6-7 postnatal weeks. The rats were divided into three case groups (E1: 4 h/d, 4 d/w; E2: 2 h/d, 4 d/w; E3: 2 h/d, 2 d/w) and one control group. The testes specimens were sectioned at 5 Î¼m and stained with the haematoxylin and eosin staining technique for histological and morphometrical studies. We found a severe decrease in germ cells associated with spermatogenesis arrest in the E1 group. A decrease in germ cells and a thickening of the basal membrane of the seminiferous tubules were seen in E2. Displacement of Sertoli and germinal cells were also found in the E3 group. The mean seminiferous tubular diameter and seminiferous epithelial height in the experimental groups were decreased in comparison with the control group and the differences were statistically significant (p < 0. 05). The findings of this study revealed that chronic formaldehyde exposure can cause histopathological and morphometric changes to the seminiferous epithelium in rats and that these changes depend on the duration of the formaldehyde exposure. Copyright © 2007 Via Medica

Azarhoush, R.

Davarian, A.

Fazeli, S.A.

Ghafari, S.

Gharravi, A.M.

Golalipour, M.J.

English

Golestan University of Medical Sciences Repository

 Folia Morphol. Vol. 66, No. 3, pp. 167–171 Copyright © 2007 Via Medica O R I G I N A L A R T I C L E ISSN 0015–5659 www.fm.viamedica.pl Formaldehyde exposure induces histopathological and morphometric changes in the rat testis M.J. Golalipour1, R. Azarhoush2, S. Ghafari1, A.M. Gharravi1, S.A. Fazeli1, A. Davarian1 1Department of Histology and Embryology, Gorgan University of Medical Sciences, Iran 2Department of Pathology, Gorgan University of Medical Sciences, Iran [Received 16 February 2007; Revised 13 June 2007; Accepted 19 June 2007] Formaldehyde is a chemical which is traditionally used for fixing cadavers and routine histopathology techniques. It is vaporised during the dissection and prac­tical study of a cadaver. Previous studies have shown that this vapour may cause clinical symptoms such as throat, eye, skin and nasal irritation. This study was designed to determine the histopathology and morphometrics of the rat testis when all the experimental animals were exposed to formaldehyde for 18 weeks. The study was performed in 2004 on 28 albino Wistar rats of 6–7 postnatal weeks. The rats were divided into three case groups (E1: 4 h/d, 4 d/w; E2: 2 h/d, 4 d/w; E3: 2 h/d, 2 d/w) and one control group. The testes specimens were sectioned at 5 µm and stained with the haematoxylin and eosin staining technique for histo­logical and morphometrical studies. We found a severe decrease in germ cells associated with spermatogenesis arrest in the E1 group. A decrease in germ cells and a thickening of the basal membrane of the seminiferous tubules were seen in E2. Displacement of Sertoli and germinal cells were also found in the E3 group. The mean seminiferous tubular diameter and seminiferous epithelial height in the ex­perimental groups were decreased in comparison with the control group and the differences were statistically significant (p < 0.05). The findings of this study revealed that chronic formaldehyde exposure can cause histopathological and morphometric changes to the seminiferous epithelium in rats and that these changes depend on the duration of the formaldehyde exposure. Key words: spermatogenesis, seminiferous epithelium diameter, seminiferous epithelial height, Sertoli, germ cell, duration INTRODUCTION Formaldehyde (CH2O) is a flammable, colourless, reactive gas, readily polymerised at normal room temperature and pressure, with a relative molecular mass of 30.03 and a pungent odour. Formaldehyde is soluble in water, ethanol and diethyl ether. It is also used in polymerised form as paraformaldehyde [23]. Under atmospheric conditions formaldehyde is readi­ly photo-oxidised by sunlight to carbon dioxide. In the absence of nitrogen dioxide the half-life of formaldehyde is approximately 50 minutes during the daytime; in the presence of nitrogen dioxide, it drops to 35 minutes [23]. There are various sources of formaldehyde, but the major anthropogenic sources which affect humans are present in indoor environments. Other anthropo­genic sources include direct emissions, especially from the production and use of formaldehyde [23]. Its potential to act as an electrophile and act with macromolecules such as DNA, RNA and protein to Address for correspondence: M.J. Golalipour, Department of Histology and Embryology, Gorgan University of Medical Sciences, Gorgan, Iran, P.O. Box: 49175-553, tel: +98 (171) 4421289, fax: +98 (171) 4425165, 4421657, e-mail: mjgolalipour@yahoo.com 167 Folia Morphol., 2007, Vol. 66, No. 3 form reversible adducts or irreversible cross-links [10] makes it useful as a conventional tissue fixative, par­ticularly for cadaver fixation. Acute formaldehyde exposure produces mainly mucosal irritation of the eye and upper respiratory tract in humans [26], and long-term exposure leads to the production of nasal tumours in rodents [15]. Formaldehyde also causes pulmonary function im­pairment [1] and asthmatic reactions in sensitised individuals [2, 6]. Some studies have indicated ter­atogenic and cytotoxic effects of formaldehyde. In one study administration of a high intraperitoneal dosage of formaldehyde caused changes in the se­miniferous epithelial cells [21]. Furthermore, in an­other study, administration of formaldehyde caused a decrease in the motility and number of spermato­zoids [14]. The present study was performed on albino Wist­ar rats with the aim of analysing the histopatholog­ical and morphometric changes in the seminiferous epithelium resulting from formaldehyde exposure in the dissection laboratory and to determine its rela­tionship with the duration of exposure. MATERIAL AND METHODS The study was performed in 2004 on 28 albino Wistar rats of 6–7 postnatal weeks (provided from the Iranian Pasteur Institute) in the Faculty of Medi­cine, Gorgan University of Medical Sciences. The rats were randomly divided into three equal case groups on the basis of the differences between the periods of exposure to formaldehyde: —	 E1 — 4 hours/day, 4 days/week for 18 weeks (4 h/d, 4 d/w); —	 E2 — 2 hours/day, 4 days/week for 18 weeks (2 h/d, 4 d/w); —	 E3 — 2 hours/day for 2 days/week for 18 weeks (2 h/d, 2 d/w). There was also a control group without any ex­posure. Approval for this study was gained from the Gor­gan University of Medical Sciences animal Care and Ethics Committee. It was found by means of a digital scale that the mean weights for each group were 252 g (E1), 209 g (E2), 222 g (E3) and 195 g (control group). The concentration of formaldehyde vapour was mea­sured at the beginning, during and at the end of the study by means of a detector tube and dragger pump (model 31, made in Germany) after the covers of the cadavers had been removed. The mean vapour concentration of the dissection room was 1.5 ppm. The temperature of the dissection room was 20–26oC and the air pressure was 760–763 atm. At non-exposure times all groups were kept in the laboratory animal quarters, which were far from the place of exposure and where no formal­dehyde was detected. The animal quarters were ventilated and the temperature kept at about 21oC; air conditioning and adequate light were supplied. All groups were fed with a similar standard diet (provided by the Iranian Pasteur Institute) twice a day (morning and afternoon) with water avail­able ad libitum. The cages of the case groups were placed at the height of a cadaver, separated by a distance of 15 cm, for 18 weeks, corresponding to the time pro­tocols mentioned above. During each period of ex­posure the control group was kept in the animal quarters. When the exposure period had expired, each of the rats of the three experiments and the con­trol group were anaesthetised with ether. After cer­vical dislocation the left testis of each experimen­tal rat was extracted. Specimens with dimensions of 4 × 4 × 2 mm were then taken from each. Af­ter tissue processing and paraffin embedding, 30 sections from each specimen, taken from the left testis, were cut at 4 µm and stained with haema­toxylin and eosin (H & E). Twenty seminiferous tu­bules in stage VI–X [9] were measured in each sec­tion. All of the sections were studied by means of an OLYMPUS light microscope with multiple mag­nifications (400 ×, 1000 ×). A morphometric study of the diameter and height of the seminiferous tubules (STD and SHE respectively) was made with the use of Olysia Autobioreport software. The data were analysed with Student’s t test and the χ² test (α = 0.05). RESULTS A severe decrease in germ cells was seen in the more than 85% of the seminiferous tubules in ani­mals of group E1. In addition, spermatozoids were rarely seen in tubules and the spermatogenesis pro­cess was arrested (Fig. 1). In group E2 a decrease in germ cells and an in­crease in thickness in the basal membrane of 75% of the tubules were found (Fig. 2). In group E3 an increase in the spaces between germ cells were seen in tubules, and the association between Sertoli and germinal cells was also disrupt­ed (Fig. 3). No histopathological changes were seen in the control specimens (Fig. 4). 168 M.J. Golalipour et al., Rat testis and formaldehyde exposure Figure 1. Histological architecture of the testis in group E1 (stage VII). Decreased germ cells (>) and arrested spermato­genesis (—>). H & E staining, 1000 ×. Figure 3. Histological architecture of the testis in group E3 (stage VI). Disruption to the arrangement of Sertoli cells and germinal cells (>). Increasing space between germ cells (—>). H & E staining, 1000 ×. Figure 2. Histological architecture of the testis in group E2 (stage VII). Decreased germ cells (>) and increased thickness of basement membrane (—>). H & E staining, 1000 ×. Figure 4. Histological architecture of the testis in the control group (stage VIII). H & E staining, 1000 ×. Table 1. Mean ± SE of seminiferous tubular diameter (STD) and seminiferous epithelial height (SEH) in experimental groups and control Control E1 (4 h/d, 4 d/w) E2 (2 h/d, 4 h/w) E3 (2 h/d, 2 d/w) STD [µm] SEH [µm] 252.12 ± 4.82* 82.77 ± 2.00** 204.55 ± 3.29* 65.26 ± 1.43** 232.45 ± 2.42* 69.46 ± 1.78** 238.94 ± 4.37* 72.80 ± 2.03** *, **control with E1, E2, E3 were significant The morphometric findings, including those for STD and SEH, are outlined in Table 1. In comparison to those of the control group the mean STD and SEH had decreased significantly (p < 0.05). In addition, a relationship was found between changes in SEH and the duration of exposure. DISCUSSION This study showed that formaldehyde exposure can cause a severe decrease in germ cells, spermato­genesis arrest and a thickening of the basement membrane of seminiferous tubules in the testis of rats. The result of this study is similar to that of other 169    Folia Morphol., 2007, Vol. 66, No. 3 research [14, 20, 21, 24, 25], although the dosage, duration and administration of formaldehyde were different in these studies. According to the study by Tang et al. [21], intrap­eritoneal administration of formaldehyde with dosag­es of 0.2, 2 and 20 mg/kg can cause degeneration and necrosis of the secondary spermatocytes, spermato­genic cells and spermatozoids. Furthermore, Chowdhury et al. [3] found disruption of the Leydig cells and spermatogenesis arrest as a result of intrap­eritoneal injection of formaldehyde at dosages of 5, 10 and 15 mg/kg in rats. Zhou et al. [24] the experimental animals to form­aldehyde vapour (10 mg/m3 for two weeks and ob­served atrophy of the seminiferous tubules, a de­crease in the number of spermatogenic cells and dis­organisation of the seminiferous epithelial cells. The Majumder and Kumar study [14] showed that formaldehyde, administered intraperitoneally at 10 mg/kg for 30 days, caused a decrease in the mo­tility, viability and number of spermatozoid cells in rats. The results of the Sarsilmaz et al. study [19] showed that exposure to formaldehyde (10 and 20 ppm) caused a severe decrease in Leydig cells in the mouse testis. The experimental study of Shah et al. [20] also showed that formaldehyde administra­tion (200 mg/kg during 10 days) can induce testis degeneration and spermatogenesis arrest. The his­tological changes among seminiferous tubules due to spermatogenesis arrest in this study are similar to the findings of Zohu’s et al. research [24]. Furthermore, the findings of our study about the decrease in spermatogenic cells were the same as those from Shah’s et al. research [20]. The morpho­metric findings of our study were in accordance with the histopathological results. Another study, which surveyed the effect of welding fumes on the se­miniferous epithelial cells in rats, showed a correlation between morphometric and histopathological chang­es [12]. With regard to the findings of our study in chronic exposure and in the normal conditions of the dissec­tion laboratory, low concentration formaldehyde exposure over a long time can be seen to cause his­topathological and morphometric alteration to the seminiferous tubules, and these changes are related to the duration of exposure. The histopathological changes in the spermato­genesis process and the seminiferous tubules have been explained by the different mechanisms. Accord­ing to the Ma et al. study [13], the histopathological changes in the spermatogenesis process and semin­iferous tubules are related to the cytotoxic effect of formaldehyde. Another mechanism was explained by Feldman [5], who reported that intraperitoneal administration of formaldehyde caused the arrest of nucleic acid synthesis and proteins. In addition, formaldehyde can increase the pro­duction of reactive oxygen species in many tissues [7, 18, 25]. Reactive oxygen species, including sin­gle oxygen, hydrogen peroxide, super oxide anions and hydroxyl radicals, are important mediators of cellular injury and play an important role in oxida­tive damage. Zhou et al. [25] also showed that form­aldehyde inhalation decreased the effectiveness of the testicular antioxidant system but brought about a prominent increase in the testicular lipid peroxida­tion product malondialdehyde in the testis of rats exposed to formaldehyde. Malondialdehyde is one of the most important products of lipid peroxida­tion and interferes with protein biosynthesis by form­ing adducts with DNA, RAN and protein [4]. Similar phenomena are often observed after exposure to chemicals and gamma radiation that cause testicu­lar damage [16, 25, 22]. This suggests that oxidative stress is an important mechanism of testicular dam­age [25]. Moreover, Ozen et al. [17] showed that subacute and subchronic formaldehyde vapour inhalation have caused growth retardation and altered levels of trace elements, including copper, zinc and iron in the tes­ticular tissue of the rat. The other possible mecha­nism in oxidative stress may therefore be due to al­tered levels of trace elements in formaldehyde expo­sure. Some research has also shown that an increase in the level of iron can cause indirect oxidative stress. This means that an increase in iron, either by mak­ing a complex with soluble cellular chelating agents such as ADP or directly by oxidative stress, can have an adverse effect on spermatogenesis [8, 11]. A de­crease in zinc and copper levels may, moreover, cause oxidative stress in the testis tissue owing to form­aldehyde exposure, as these two trace elements are co-factors of zinc-copper cytoplasmic superoxide dismutase (Zn, Cu-SOD) [8]. In conclusion, the results of this study showed that chronic formaldehyde exposure at the concentration and duration mentioned can cause histopathological and morphometric alterations in the seminiferous epithelium in rats. In addition, it seems that there is a relationship between the severity of exposure­-induced changes and the duration of exposure. 170 M.J. Golalipour et al., Rat testis and formaldehyde exposure ACKNOWLEDGEMENTS The authors would like to express their apprecia­tion of the Department of Research Gorgan Univer­sity of Medical Sciences for financial support and are particularly grateful to Mr. Moludi and Ms Irani. In addition, we are indebted to Prof. Boldaji, who guided us through the study. REFERENCES 1.	 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Formaldehyde exposure induces histopathological and morphometric changes in the rat testis

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Formaldehyde exposure induces histopathological and morphometric changes in the rat testis

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