Background

Plant growth regulators (PGRs) usually are defined as endogenous plant hormones which are produced naturally by plants and are essential for regulating growth, formation of leaves and flowers, elongation of stems, and development and ripening of fruits. PGRs are classified into 5 types as auxins, gibberellins, cytokinins, ethylene, and abscisic acid. The gibberellins represent the important item of plant growth hormones. Gibberellins were discovered isolated whereas there are at least 136 Gibberellin types (Boğa et al., 2009). Gibberellins (GAs) are plant hormones which control various processes such as stem elongation, stem germination, dormancy, flowering, sex expression, enzyme induction, and fruit senescence (Rios-Iribe, et al., 2011; Rangaswamy, 2012). Gibberellic acid (GA3) is accumulated in the soil for months (Schwechheimer and Willige, 2009). Exposure to residues of GA3 as a result of consumption of different kinds of exposed vegetables and fruits causes toxicity and hazardous effects on the health of human and animals (Tomlin, 2004). GA3 has been documented to alter the antioxidative systems and production of free radicals in some organs (Celik and Tuluce, 2006). GA3 is considered carcinogenic and induce tumor formation (El-Mofty et al.,1994). It affects the sexual differentiation and the fecundity of mammals (Ozmen et al., 1995).

Vegetable oils are considered an important source of antioxidants (Ramadan and Moersel, 2006). Olive oil is obtained from the fruit Olea europaea and has been used since ancient times in the traditional medicine, skin protectants, cosmetics, soaps, bath oils, creams, and perfumes (Brun, 2000). Olive oil contains multiple bioactive and antioxidant components, e.g., vitamins (alpha- and gamma-tocopherol and betacarotene), phytosterols, squalene, pigments, terpenic acids, flavonoids (luteolin and quercetin), polyphenols, unsaturated fatty acids (oleic, linoleic and linolenic acids), microconstituents (e.g., phenolic compounds in the unsaponifiable fraction), and micronutrients (A, E and b-carotene) (Visioli and Galli, 2002; Covas, 2007). The healthful properties of olive oil are attributed to its contents of a series of phenolic components, e.g., hydroxytyrosol, tyrosol, oleuropein, and ligostride (Omar, 2010). In addition, olive oil contains decarboxymethyl ligstroside aglycone that is considered a natural anti-inflammatory substance which counteracts the inflammatory processes (Parkinson and Keast, 2014; Rosillo et al., 2014). Pharma-nutritional evidence from the last decade indicates that olive oil has an important role in cardioprotection and prevents neurodegenerative diseases, e.g., Alzheimer’s disease (AD), Parkinson’s disease (PD), and mitigating the spinal cord injury (SCI). In addition, olive oil has antimicrobial, hypoglycemic, anti-inflammatory, antioxidant, and anti-hypertension and is beneficial to wound healing process and antiviral (Crespo et al., 2018; Figueiredo-González et al., 2018). Olive oil was documented as having anti-oncogenic activity and anti-cancer especially colorectal and breast cancer (Menendez and Lupu, 2006; Pelucchi et al., 2011) and decreases chronic disease such as cardiovascular diseases (CVD) (Ruiz-Canela and Martínez-González, 2011) and atherosclerosis (Kok and Kromhout, 2004). Health-protective effects of olive oil have been traditionally due to its high content of monounsaturated fatty acid mostly in the form of oleic acid (Escrich et al., 2011; Bermudez et al.,2011). Olive oil biophenols have potential preventive actions against cancer by inhibition of cell proliferation and tumor progression (Crespo et al., 2018). Therefore, the aim of the work is to investigate the counter effect of olive oil against GA3-induced embryotoxicity during prenatal stages of mice.

Materials and methods

Gibberellic acid (GA3)

Berelex tablet (10 g) contains 10% GA3 and manufactured by Valent BioSciences Corporation, Illinois, USA. Stock solution was prepared in saline and renewed as required during the experimental period.

Olive oil

Virgin olive oil (VOO) was purchased from a local market. VOO contained 68.23% of monounsaturates (mainly oleic acid), 16.29% of saturates (palmitic and stearic acids), and 14.21% of polyunsaturated fatty acid.

Experimental procedure and animal grouping

Immature mice (3 weeks old) Mus musculus were obtained from animal house of Sohag University. Animals were acclimatized in laboratory at normal light and temperature conditions with free access to food and water till maturity. In a preliminary experiment, 18 mature females were divided into control and GA3 oral daily exposed for 1 week with ascending doses of GA3 (55, 110, 240, 480, 960 mg/kg B.W.). The exposed females (3 animals each) for each dose were mated with one mature male with continuous dosing for an additional week. Females were dissected for pregnancy clarification. In the second experiment, 20 pregnant female mice (25–30 g) at the 7th day of gestation were divided into four groups (five females in each group). Group 1 served as controls. Group 2 received GA3 through drinking water (55 mg/kg equivalent to 1/100 of LD 50) (Troudi et al.,2011; El-Sayyed et al. 2012). Group 3 was treated with olive oil (16.6 ml/kg. B. W.) via gastric gavage. The dose of olive oil is relatively similar to the Mediterranean diet style of olive oil consumption (Esposito et al., 2004). Group 4 combined administered with GA3 and olive oil. The experimental groups were kept under experimentation from the 7th day of pregnancy up to the 18th day. The use of studied animals and experimental protocol complied according to the guidance of ARRIVE guidelines and the Institute of Laboratory Animal Resources (ILAR, 1986; Kilkenny et al.,2010).

Histological and immunohistochemical examinations

The tissues from the first experiment (ovaries and uteri of control and GA3-treated groups) and from the second experiment (embryos at E14 and E18 at studied groups) were fixed in Carnoy’s fixative. The fixed tissues were dehydrated in absolute ethanol, cleared in methyl benzoate, and infiltrated in paraffin wax. The paraffin blocks of studied tissues were cut at 5 μm thick by microtome (RM 2125RTS; Leica Biosystems, Shanghai, China). The paraffin sections were mounted on glass slides and dried at 40 °C in an oven for 3 days. Selected sections of the first experiment (uterus, ovary) and from the second experiment (developing liver, kidney, skin at E14 and E18) were stained with hematoxylin and eosin for general histological picture and with periodic acid Schiff’s (PAS) reaction for polysaccharide detection (Drury and Wallington, 1976).

In the immunohistochemical study, the selected sections of the first experiment (uterus, ovary) and from the second experiment (developing liver, kidney, skin at E14 and E18) were mounted on positive slides (Superfrost/Plus). According to the manufacturer’s protocol of Spring Bioscience company, the selected sections were deparaffinized in xylene, rehydrated in descending alcohol series (100, 90, 70, 50%), and retrieved for re-antigenicity using citrate buffer (10 mM, pH = 6) in an oven at 100 °C for an hour (Buchlowalow and Bocker, 2010). Sections were treated for 10 min with 3% hydrogen peroxide block and then with protein block (phosphate buffer solution, pH 7.6, with 0.5% BSA, 0.5% casein, and less than 0.1% sodium azide) for 10 min to block nonspecific background staining. Sections were incubated with primary antibody (tumor necrosis factor receptor 2, TNFR2) (Rabbit polyclonal, Spring Bioscience, USA). The washing step was carried out by using phosphate buffer (pH = 7.4) for three times. Sections were incubated with biotinylated goat anti-polyvalent in phosphate buffer for 30 min. Then, sections were incubated with Streptavidin Peroxidase for 30 min. Sections were immersed in freshly preparation of solution (20 μl of DAB Chromogen (3, 3′-diaminobenzidin) + 1 ml of DAB substrate) for 15 min. Sections were dehydrated in ascending series of ethanol (50%, 70%, 90%, 100%). The clearing process occurred by xylene and mounting by using DPX mounting media. Selected sections of adult tissues (uterus, ovary) and developing tissues at E14 and E18 days (liver, kidney, skin) were photographed as required. Imaging were made using a light microscope (Axiolab Standart 20, Carl Zeiss, Germany) provided with camera (Axion Cam, Carl Zeiss, Germany).

Results

Uterine and ovarian tissues

The histological structure of the control uterus showed the normal uterine folds in the endometrium (Fig. 1a, c). GA3-treated group (110 mg/kg B.W.) provoked a decrease of uterine folds and an increase of pyknotic cells (Fig. 1b, d). The uterine gland of control uterus showed a positive carbohydrate reaction (PAS) (Fig. 1e), whereas the GA3-treated group (110 mg/kg B.W.) showed negatively staining of carbohydrate contents in the uterine glands (Fig. 1f). Immunohistochemical study showed positive localization of TNFR2 in control uterine glands (Fig. 2a) that was absent in the luminal epithelium except its apical cell surface (Fig. 2c). GA3-treated group (110 mg/kg B.W.) showed decrease in the TNFR2 expression in the uterine glands (Fig. 2b) and alteration in the expression of luminal epithelium that was detected throughout the cells (Fig. 2d). Treating animals with GA3 for a continuous 2 weeks causes histopathological alterations in the ovary including severe degeneration of the ovarian follicles and congestion of blood vessels (Fig. 3b, d) as compared to the normal structure in control (Fig. 3a, c). Degenerated follicles in the ovary of GA3-treated group showed alteration in the carbohydrates content (Fig. 3f) as compared to the normal localization in the oocyte membrane of control (Fig. 3e). TNFR2 expression was detected in the zona pellucida of control ovary (Fig. 3g), whereas ovarian toxicity with GA3 showed undistinguished TNFR2 expression in zona pellucida with an increase in the expression of zona granulosa cells (Fig. 3h).

Fig. 1
figure 1

Photomicrographs of histological sections (H&E and PAS). Control uterus showed normal structure (a, c). GA3-treated showed a decrease of uterine folds and an increase of pyknotic cells (arrow, b, d). Uterine gland of GA3-treated group showed a decrease of PAS content (arrow, f) as compared to control PAS (arrow, e). MM, myometrium; EM, endometrium; LE, luminal epithelium; S, stroma; GE, glandular epithelium. Scale bar = 50 μm (a, b) and 10 μm (c–e)

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Fig. 2
figure 2

Photomicrographs of immuno-stained sections of uterine tissues showed TNFR2 expression in the control uterine gland (arrow, a). GA3-treated group showed a decrease in TNFR2 expression in the uterine gland (arrow, b). High magnification field showed alteration in TNFR2 expression of the endometrium (d) as compared to control (c). MM, myometrium; EM, endometrium; LE, luminal epithelium; S, stroma; GE, glandular epithelium. Scale bar = 50 μm (a, b) and 10 μm (c, d)

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Fig. 3
figure 3

Photomicrographs of H&E-, PAS-, and TNFR2 immuno-stained sections in the ovary. Normal histological structure was observed in control ovary (a, c). GA3-treated group showed congestion of blood vessel (red arrow, b), degeneration of the follicles (black arrow, b), and vacuolation (black arrow, d). GA3-treated group showed alteration in the carbohydrates content (PAS) (arrow, f) as compared to the normal localization in the zona pellucida of control ovary (arrow, e). TNFR2 expression was detected in the zona pellucida of control ovary (arrow, g), whereas GA3-treated ovary showed undistinguished TNFR2 expression in zona pellucida (black arrow, h) with increase the TNFR2 expression in zona granulosa cells (red arrow, h). O, oocyte; F, follicle; N, nucleus; ZP, zona pellucida; ZG, zona granulose; TI, theca interna; TE, theca externa. Scale bar = 50 μm (a, b) and 10 μm (c–h)

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Liver

The control liver at E14 of gestation showed normal hematopoietic tissue. PAS-stained sections showed positive megakaryocytes (Fig. 4b). TNFR2 expression was localized in the blood vessel of the developing liver with pale or faint expression in hepatic parenchyma (Fig. 4c). In GA3-treated embryo, the developing liver showed vacuolation of hematopoietic tissue that was associated with increase inflammatory cells (Fig. 4d). GA3-treated embryo showed an increase in the abundance of megakaryocytes in the PAS-stained sections (Fig. 4e) and downregulation of TNFR2 expression (Fig. 4f) as compared to control. The olive oil-treated group elucidated similarity to the control group regarding the structure of hematopoietic tissue, positive megakaryocytes, in addition to increased TNFR2 expression along to the endothelial lining of the blood vessels (Fig. 4g–i). The olive oil-treated GA3 group showed improvement in the alterations induced by GA3 (Fig. 4j–l). The developing liver at E14 of gestation in the studied groups showed a negative stain of glycogen. The control liver at E18 of gestation showed hematopoietic tissue and developing hepatocytes which contact with each other to form hepatic cords (Fig. 5a). Hepatocytes of the developing liver in control revealed regularly positive stainability to carbohydrate content (PAS staining) throughout the hepatic parenchyma (Fig. 5b). TNFR2 expression was observed in the blood vessel and in some hepatocytes (Fig. 5c). The hematoxylin and eosin-stained sections of the developing liver at E18 in GA3-treated embryo showed pale-staining of less viable tissue, difficulty to differentiate the nuclei and decline in erythropoietic activity (Fig. 5d). In GA3-treated embryos, the developing liver revealed depletion of hepatic parenchyma in PAS stainability (Fig. 5e) and downregulation of the TNFR2 expression (Fig. 5f) as compared to control. In olive oil-treated embryos, the histological (H&E) and histochemical (PAS) stains of developing liver at E18 revealed similarity to control group (Fig. 5g, h). An increase of TNFR2 expression was observed in the hepatic tissue of olive oil-treated embryos (Fig. 5i) as compared to control. The GA3-olive oil-treated group showed improvement of the alterations that is induced by GA3 at the level of histology (H&E), histochemistry (PAS), and immunohistochemistry (TNFR2) (Fig. 5j–l).

Fig. 4
figure 4

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing liver at E14. The control liver showed normal structure of hematopoietic tissue, positive megakaryocytes in PAS reaction (black arrow, b), and TNFR2 expression was localized in blood vessel (black arrow, c). GA3-treated group exhibited loosely arranged hematopoietic cells (black arrow, d), pyknotic cells (red arrow, d), increase the number of megakaryocytes in PAS reaction (arrow, e), and decrease TNFR2 expression (arrow, f). Olive oil-treated embryo did not exhibit any histopathological alteration (g, arrow h, arrow i). GA3-olive oil- treated embryo showed improvement in the GA3 alterations (j, arrow k, arrow l). BV, blood vessel; H, hematopoietic. Scale bar (a–l) = 10 μm

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Fig. 5
figure 5

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing liver at E18. The control liver showed normal structure of hepatic cord, positive carbohydrates (red arrow, b), and TNFR2 expression was localized in blood vessel and in some hepatocytes (black arrow, c). GA3-treated group exhibited loosely arranged hepatic cords with pale-staining and vacuolation (black arrow, d), decrease the PAS reaction (red arrow, e), and decrease TNFR2 expression (black arrow, f). Olive oil-treated embryo did not exhibit any alteration in H&E and PAS (g, arrow h) but showed an increase of TNFR2 expression (black arrow, i). GA3-olive oil-treated embryo showed improvement in the GA3 alterations (j, arrow k, arrow l). BV, blood vessel; HC, hepatic cords. Scale bar (a–l) = 10 μm

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Kidney

The developing kidney at E14 of gestation in the studied groups showed glomeruli and tubules. There are no abrupt histopathological changes that were observed in the developing kidney at E14 at the level of H&E, PAS, and TNFR2 stains in the studied groups, GA3 (Fig. 6d–f), olive oil (Fig. 6g–i), and GA3-olive oil (Fig. 6j–l), as compared to control (Fig. 6a–c). The control kidney at E18 of gestation showed well-developed Bowman-s capsules, glomeruli, and tubules (Fig. 7a). PAS-stained sections of control kidney at E18 revealed positively stained brush border of proximal convoluted tubules and glomeruli (Fig. 7b). TNFR2 expression was localized in the kidney tubules (Fig. 7c). The kidney of GA3-treated embryos revealed pale-staining, degeneration of renal tubules, and shrinkage of renal corpuscles (Fig. 7d) as compared to the control. Depletion of polysaccharides in brush border and the glomeruli (PAS stain) (Fig. 7e) and downregulation of TNFR2 expression were observed in the kidney of GA3-treated embryos. Olive oil-treated embryo showed similar kidney structure of control but an increase in the expression of TNFR2 was noted (Fig. 7g–i). The kidney in the GA3-olive oil-treated embryos revealed improvement in the alterations that is induced by GA3 (Fig. 7j–l).

Fig. 6
figure 6

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing kidney at E14. The developing kidney at E14 of gestation in the studied groups showed glomeruli (G) and tubules (T). There is no histopathological alteration noted in the developing kidney at E14 at the level of H&E, PAS, and TNFR2 stains in the studied groups; GA3 (d–f), olive oil (g–i), GA3-olive oil (j–l) as compared to control (a–c). Scale bar (a–l) = 10 μm

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Fig. 7
figure 7

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing kidney at E18. The control of developing kidney at E18 of gestation showed glomerulus (G), and tubules (T) (a). The kidney tubules showed positive carbohydrates (PAS reaction) (b) and TNFR2 expression (c). GA3-treated embryos revealed kidney of pale-staining, tubule degeneration, shrinkage of renal corpuscles (arrow, d), decrease stainability of carbohydrates (e) and TNFR2 localization (f). Olive oil-treated embryo showed similar kidney structure such that observed in the control but an increase in the expression of TNFR2 was noted (g–i). The kidney in the GA3-olive oil-treated embryos revealed improvement in the alterations that induced by GA3 (j–l). Scale bar (a–l) = 10 μm

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Skin

The skin at E14 of gestation showed epidermis and dermis. The epidermal layer is characterized by primordia of hair follicles that are surrounded by dense mesenchyme of the dermis (Fig. 8a). The carbohydrates were detected in the basement membrane of the epidermis (Fig. 8b). TNFR2 expression was localized in the dermal layer (Fig. 8c). The skin of GA3-treated embryos revealed a thin epidermis with poor development of primordial hair follicles that was associated with vacuolization and pyknotic cells (Fig. 8d). Decrease in the epidermal PAS staining (Fig. 8e) and TNFR2 expression (Fig. 8f) was noted in the GA3-treated embryo. The H&E- and PAS-stained sections in the skin of olive oil-treated embryos showed similar structure to the control (Fig. 8g, h) but an increase of TNFR2 expression was observed (Fig. 8i). Improvement in the histopathological changes was noted in GA3-olive oil treatment (Fig. 8j–l). The control skin at E18 consists of well-differentiated layers: Malpighian, stratum spinosum, stratum granulosum, stratum cornium, and a well-developed hair follicle (Fig. 9a). PAS- and TNFR2-stained skin sections revealed localization of carbohydrates and TNFR2 expression in the epidermal layer (Fig. 9b, c). The histological, histochemical, and immunohistochemical alterations induced by GA3 were concomitant with a thin wrinkled epidermis, a less abundant and disorganized hair follicles with shrinkage of dermal papilla and decrease in PAS and TNFR2 expression in the epidermal layer (Fig. 9d–f) as compared to control. H&E- and PAS-stained sections in the skin of olive oil-treated embryo showed similarity to control. High TNFR2 expression was noted in the epidermis and dermis of skin of olive oil-treated embryo (Fig.9i). The skin of GA3-olive oil-treated embryos showed improvement in the H&E, PAS, and TNFR2 expression as compared with skin of GA3-treated embryo (Fig. 9j–l).

Fig. 8
figure 8

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing skin at E14. The skin consists of the epidermis (Ep), hair follicles primordium (FP), and dermis. The control skin showed positive carbohydrates in the basement membrane of the FP (b) and TNFR2 expression in the dermis (c). The skin of GA3-treated embryos showed a thin Ep with poor development of FP, decrease carbohydrate content, and downregulation of TNFR2 expression. The skin of olive oil-treated embryos showed similar structure to the control (g, h) but an increase of TNFR2 expression was observed (i). Improvement in the histopathological changes was noted in the skin of GA3-olive oil-treated embryos (j–l). Scale bar (a–l) = 10 μm

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Fig. 9
figure 9

Photomicrographs of H&E-, PAS-, and TNFR2-stained sections of developing skin at E18. The control skin contains Malpighian (M), stratum spinosum (SS), stratum granulosum (SG), stratum cornium (SC), and a well-developed hair follicle (HF) (a). PAS- and TNFR2-stained skin sections revealed localization of carbohydrates and TNFR2 expression in the epidermis (b, c). The skin of GA3-treated embryos showed a thin wrinkled epidermis, a less abundant and disorganized hair follicles with shrinkage of dermal papilla and decrease in PAS and TNFR2 expression in the epidermis (d–f). The skin of olive oil-treated embryo showed H&E and PAS staining similar to control, but high TNFR2 expression (i). The skin of GA3-olive oil-treated embryos showed improvement in the histopathological changes (j–l). Scale bar (a–l) = 10 μm

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Discussion

The present study showed histopathological changes after treatment with GA3 in the adult tissues (uterus, ovary) and developing tissues (liver, kidney, skin) of mice at prenatal stages E14, E18 at the level of histology (H&E), histochemistry (PAS), and immunohistochemistry of TNFR2. Previous studies reported that GA3 induces histopathological and biochemical alterations in the ovary of albino rats at a dose of 50 mg/kg B.W. of GA3 for 4 weeks (Lamfon, 2013). GA3 toxicity was documented in adult rats and their progeny (Troudi et al.,2010). In the same context, GA3 has transplacental passage properties and affects the fetal tissues (Alsemeh et al., 2019). Exposure to GA3 causes teratogenicity in the Xenopus embryos and in the albino rat, whereas the live embryos have severe negative effects by accumulation (Boğa et al., 2009; El-Sayyad et al., 2012). GA3 also induces abnormal development of the external morphology and ossification of rat skeleton (El-Sayyad et al., 2012). Oral exposure of GA3 to Wistar rats during late pregnancy, lactation, and early postnatal periods causes histopathological alteration in the suckling rats and their mothers (Troudi et al.,2011). Abnormal biochemical parameters of brain, liver, and kidney were reported after exposure to GA3 (Troudi et al., 2012; Abdel Rahm et al.,2017). The harmful effects induced by Gibberellic acid were attributed to inducing oxidative stress, reactive oxygen species (ROS) that oxidize and attack the vital cellular component to initiate or progress the cellular damage (Stadtman and Levine, 2000). Other factors such as impairment of the antioxidant enzymes system, reducing cellular defense system, and production of free radicals that account to the histopathological alteration induced by GA3 were reported (Halliwell and Gutteridge, 1999; Troudi et al., 2010). Exposure to GA3-induced damage of DNA of the cells due to oxidative stress that was caused by reactive oxygen species (Chen et al. 2012). The current study showed a decrease of the carbohydrate contents during the development of the liver, kidney, and skin in the GA3-treated group. Similar reports indicated a failure of energy preservation after exposure to insecticides. Also, during stress, more energy will be needed to get rid of the toxicants and minimizing the dangerous effects (Sharma and Agarwal, 2004; Seleem, 2019).

Olive oil was found to contain a mix of phenolic compounds such as oleuropein and hydroxytyrosol which have therapeutic capabilities and scavenging abilities, e.g., decrease ROS production, malondialdehyde (MDA), and downregulate of cyclooxygenase 2 (COX-2) expression and inducible nitric oxide synthase (iNOS) (Camargo et al., 2014; Incani et al., 2016). Oleuropein and hydroxytyrosol assert their anti-inflammatory properties by several mechanisms, e.g., effect on cytosolic Ca2+ levels, reduction of cytokines IL-α and TNF-α, decreasing the number of infiltrating neutrophils, and activation T and B lymphocytes (Gong et al.,2009; Zbidi et al.,2009). Oleuropein and hydroxytyrosol showed protective effects on vascular endothelial cells by limiting oxidative injury and inflammatory damage mediated by TNF-α Zrelli et al., 2011). Administration of olive oil with hydroxytyrosol is beneficial in acute inflammation and rheumatoid arthritis; it decreases paw edema, bone resorption, inducible nitric oxide, and osteophyte formation, inhibiting cancer cell lines of breast, prostate, and colon (Silva et al., 2015; Rosignoli et al., 2016). In addition, olive oil with its phenolic compound has been shown inhibitory effects on neovascularization and angiogenesis abrogation by inhibition of MMP-2, MMP-9 activity, and downregulation of VEGF expression (Scoditti et al., 2012; Lamy et al., 2014). In the same scenario, ingestion of phenol-rich olive oil exerts positive regulatory effects on neuronal function and chemopreventive effects of DNA damage and modulates the expression of microRNAs in mothers and offspring during pregnancy and reduces inflammatory action that is caused by joint-degenerative and neurodegenerative diseases (Casas-Agustench et al., 2015; Luceri et al., 2017). Moreover, administration of phenolic-rich olive improves neurologic deficit, counteract age-related dysfunctions, and reduces brain edema and blood-brain barrier permeability (Pitozzi et al., 2012; Rabiei et al., 2013).

Inhibition of TNFR2 expression was noted in the GA3-treated group that might be attributed to losing the viability of cells to synthesize required factors to maintain its normal life function under the stress of GA3 toxicity. A previous study documented the reduction of TNFR2 expression alongside blood sinusoids in adult liver tissue and decrease TNFR2 expression in glomerulus, extracellular matrix, and tubules in adult kidney after exposure to GA3 (Seleem and Hussein, 2018). Also, TNF expression was decreased after arsenic exposure (Hermann and Kim, 2005). Clothianidin insecticide inhibits TNF-α expression (Di Prisco et al.,2017). The reduction of TNF expression might be due to activation of death domain in TNFR causing apoptosis, whereas the receptors recruit procaspase-8 and procraspase-3 that mediate an apoptotic pathway in mammalian cells (Chang et al.,2003). The present study showed an increase in the expression of TNFR2 in the olive oil-treated group in the studied tissues. Our results were supported with previous observations in which the consumption of olive oil increased gene expression of some factors, e.g., brain-derived neurotrophic factor in the prefrontal cortex of rats (Zrelli et al., 2011; Ayissi et al., 2014). Also, administration of olive oil in pregnancy and breastfeeding may increase fibroblast growth factors (FGF-2) mRNA expression (Pase et al., 2015). Limited information is available about the effect of olive oil on TNFR2 and immune system. The maternal diet of olive oil can decrease the plasma pro-inflammatory cytokine levels and regulates some growth factors (Shen et al., 2015; Pase et al., 2015) that may be attributed to the high contents of monounsaturated fatty acids in olive oil (Ayissi et al., 2014). The administration of olive oil exerts beneficial effects on the immune system (Puertollano et al., 2010) that may be attributed to oleic acid in olive oil components (Puertollano et al., 2007).

Many attempts have been carried out to countereffect the toxicity of GA3 as using phycocyanin, pomegranate peel extracts, and grape seeds proanthocyanidin extract, terbium gibberellic complex by their ability as a scavenger of oxygen radicals or antioxidant properties (Hussein et al., 2015; Seleem and Hussein, 2018; Khalaf et al., 2019). In the same context, previous studies which administrated Nigella sativa oil, silymarin, and vitamin C to reduce the histopathological alteration induced by GA3 during rat embryogenesis were conducted (Ali et al., 2018; Alsemeh et al., 2019). The current study used olive oil to counteract the GA3 toxicity that led to a marked improvement in the histopathological changes occurring in the developing liver, kidney, and skin. Olive oil was reported in protection of embryos and newborns during pregnancy and breastfeeding (Trapani et al., 2017). Olive oil consumption during pregnancy prevents wheezing in children, asthma development, and atopy in children (Chatzi and Kogevinas, 2009; Trapani et al., 2017). Also, oral administration and topical application of olive oil used in the treatment of wounds and burns of skin conditions in infants and neonates (Sakazaki et al., 2007; Kiechl-Kohlendorfer et al., 2008). Administration of pregnant women with healthy diet contain olive oil reduces risk postpartum depressive symptoms, protect their children from expected dangers, and influence the urinary metabolome of nursing mothers and the health of breastfed children (Chatzi et al., 2011; Silva et al., 2015). Also, supplementation of olive oil is considered protective against hepatotoxicity induced in male Wistar rats and protects red blood cells from oxidative damage (Paiva-Martins et al.,2015; Kalaiselvan et al., 2016).

Conclusion

The present study was conducted to evaluate the ameliorative effect of olive oil on GA3-induced embryonic defects during mice gestation. From the presented data, it is obvious that olive oil supplementation during pregnancy ameliorates the defects induced with GA3 at both histological and immunohistochemical levels of the developing liver, kidney, and skin. The study recommended to consider olive oil as a protective agent against the hazardous effects of plant regulators that are widely used and reach the developing embryos during intrauterine development.