Open Access

Effect of Launaea procumbens on thyroid glands lipid peroxidation and hormonal dysfunction: a randomized control trial

Lipids in Health and Disease201716:168

https://doi.org/10.1186/s12944-017-0557-8

Received: 16 May 2017

Accepted: 31 August 2017

Published: 11 September 2017

Abstract

Background

Launaea procumbens (Roxb.) Amin is traditionally used in Pakistan for the treatment of hormonal disorders and oxidative stress. The present study was aimed to evaluate the efficacy of Launaea procumbens methanol extract (LPME) against KBrO3-induced oxidative stress and hormonal dysfunction in thyroid.

Methods

To examine the effects of LPME against the oxidative stress of KBrO3 in thyroid tissue, 36 male albino rats were used. Protective effects of LPME were observed on thyroid hormonal levels, activities of antioxidant enzymes, lipid peroxidation (TBARS) and DNA damage.

Results

Treatment with KBrO3 significantly (P < 0.01) reduced the levels of T3 (55.13 ± 1.93) and T4 (14.7 ± 1.78) and increased TSH (55.13 ± 1.93) levels. KBrO3 exposure in rats reduced the activities of antioxidant enzymes viz.; CAT (1.16 ± 0.08); SOD (12.0 ± 0.08), GST (17.7 ± 1.1) and GSR (54.3 ± 2.1) but increased lipid peroxidation (20.3 ± 0.71) and DNA (30.4 ± 2.0) damage. Co-administration of LPME significantly (P < 0.01) improved these alterations with respect to hormonal levels, activities of antioxidant enzymes and lipid peroxidation close to those seen in control rats.

Conclusion

These results suggest that LPME can protect thyroid tissue against oxidative damage, possibly through the antioxidant effects of its bioactive compounds.

Keywords

Launaea Procumbens Oxidative stressAntioxidant enzymesT3 T4

Background

Potassium bromate (KBrO3) molecular weight 166 g/mol is an oxidizing agent. KBrO3 has been used is in industries for the formation of hair solution and cosmetics. Potassium bromate is formed as by product during ozonization of water, causes infections and has been classified as 2B group toxic chemical a probable human carcinogen [9]. KBrO3 causes renal cell and thyroid carcinomas in rats, hamsters and mice when exposed chronically [15]. It has been investigated that potassium bromate produces free oxygen radicals which causes oxidative stress and DNA damages [20]. KBrO3 causes nephrotoxicity and hepatotoxicity; decreases the tissue soluble proteins, antioxidant enzymes. The decrease of antioxidant enzymes are due to reactive oxygen species (ROS) produced by metabolism of potassium bromate. Potassium bromate depleted GSH content in various tissues which causes decrease in phase II metabolizing enzymes like GSH-Px and glutathione reductase (GSR). It also increases TBARS contents, causes lipid peroxidation and disrupts liver profile including γ-GT, ALP and protein concentration [4]. Medicinal plants and nutraceuticals play important role in improving human health and phytomedicine [24]. These medicinal plants are composed of some bioactive phytochemical substances, regulates various physiological and molecular action in living organisms. Today many natural products extracted from medicinal plants are being tested for the presence of new drugs with new modes of pharmacological action. Special features of higher plants are their capacity to produce a large number of secondary metabolites [2].

Launaea procumbens (Roxb.)Amin. (Asteraceae) is an annual herb having simple leaves and yellow flowers found in waste places, vacant lots and in cultivated fields throughout Pakistan. Launaea procumbens was used as a food and washing agent [27] rheumatism, galactogogues, and increases milk production. Eye redness and itchiness are treated with Launaeaprocumbens and also traditionally used in kidney (painful urination), liver and sexual diseases like gonorrhoea [23]. The antimicrobial activity of ethanolic and aqueous fractions of Launaeaprocumbens was checked against various bacterial and fungal pathogens and reported that proved that ethanolic extract show maximum activity while theaqueous extract was inactive. Launaea procumbensis generly classified as, Kingdom (Plantae), Order (Asterales), Family (Asteraceae), Tribe (Cichorieae), Genus (Launaea), and Species (procumbens). Chemical characterization showed that Launaeaprocumbens composed of salicylic acid, vanllic acid, synergic acid, 2-methyl-resercinol, gallic acid and used against plant pathogenic fungi, nematocides and as allelopathic for inhibition of plant growth [26].

In the present research work we arranged to investigate the protective effects of plant extracts against KBrO3induced thyroid dysfunctions in rats.

Methods

Plant collection and extraction

Launaea procumbens whole plant was collected from District Bannu during summer season 2016. After shad drying of plant at room temperature (25 °C), it was ground mechanically to get fine powder. Among powder, 1 kg of fine powder was socked in 70% methanol (1.5 L) and shacked randomly. After a week the extract was filtered viaWhatman filter paper No.1. Filtrate was concentrated using rotary evaporator at 38 °C to get methanol crude extractand was kept at 4 °C in the refrigerator for further in vitro investigation.

Experimental procedure

Sprague-Dawley male rats were divided into sixteen groups (06 rats). Group 1 was control while Group II received DMSO and saline (0.20% aqueous NaCl solution) orally (Wednesday and Saturday) at a dose of 3 ml/kg b.w. Group III was administered high purity grade KBrO3 (99.9%) 20 mg/kg b.w in 0.20% aqueous NaCl solution (Monday and Thursday) intragastrictly. Group IV and V were given 100; 200 mg/kg b.w of crude methanol extract (Wednesday and Saturday) of L. procumbens (LPME) after 48 h of KBrO3 treatment. However, Group VI was given only (LPME) at a dose of 200 mg/kg b.w (Wednesday and Saturday). All these treatments were given twice a week for 4 weeks. After completion of experiment all the animals were kept on normal feed without any treatment for at least 24 h before the dissection of animals. Animals were given chloroform anesthesia after urine collection and dissected from ventral side. Blood was collected in the falcon tube and centrifuged for serum and stored in refrigerator. Thyroid glandwas removed and washed in ice cold saline, dried with blotting paper and weighted. After weighing the tissues were divided into two portions. One part was cut off and stored in fixative sera for histology while the other portion was treated with liquid N2 and stored at −70 °C for further biochemical and molecular studies.

Serum biochemistry

Serum level of various hormones viz.; T3, T4and TSHwere calculated through 10,227-Czch Republic (IM1447-IM3286) Kit purchased from IMMUNOTECH Company.

Antioxidant oxidant profile

Eighty mg tissue of thyroid tissue was homogenized in phosphatebuffer for 20 min at 4 °C and centrifuged at 10,000 rpm to obtain supernatant. Total tissue protein [16] and antioxidant enzymes like CAT and POD [3], SOD [12], γ-GT [6], GSH [1], TBARS [11], GSH-Px, GSR and GST [19, 21, 22], H2O2, and QR [10] respectively.

Genotoxicity assays

DNA damages were assessed using protocol of Wu et al. [28] qualitatively as well as quantitatively.

Histopathalogical studies

Cellular changes were observed light microscope at 40×.

Statistical analysis

To determine the treatment effects one way analysis of variance was carried by computer software SPSS 13.0. Level of significance among the various treatments was determined by LSD at 0.05% level of probability.

Results

Serum Biochemistry

Effects of methanol fraction on the serum level of thyroid hormones like TSH, T3 and T4 are shown in Table 1. Treatment of KBrO3 caused reduction in the secretion of T3, T4 and increased the secretion of TSH comparatively to non treated rats. Co-administration of LPME significantly decreased the hormonal secretion in a dose dependent way.
Table 1

Serum biochemistry

Treatment

TSH (ng/dl)

T4 (ng/ml)

T3 (ng/ml)

Control

35.53 ± 1.56++

10.0 ± 2.06++

23.2 ± 1.87++

DMSO + olive oil

34.67 ± 1.75++

9.50 ± 1.04++

22.6 ± 1.94 ++

20 mg/kg KBrO3

55.13 ± 1.93a

6.0 ± 1.32a

14.7 ± 1.78a

100 mg/kg LPME+ KBrO3

42.07 ± 1.84++

8.5 ± 1.24++

26.43 ± 2.4++

200 mg/kg LPME+ KBrO3

36.87 ± 2.02++

9.3 ± 1.06++

24.50 ± 1.75++

200 mg/kg LPME alone

34.0 ± 2.0++

10.7 ± 1.19++

21.67 ± 2.16++

Mean ± SE (n = 6 number)

aIndicate significance from the control group at P < 0.01 probability level

++ Indicate significance from the KBrO3 group at P < 0.01 probability level

Assessment of antioxidant profile

Antioxidant enzymes play a crucial role in detoxification of free radicals. KBrO3 induction in rats significantly (p > 0.01) decreased the amount of tissue soluble protein and activities of first level antioxidant enzymes viz.; CAT, POD and SOD as compare to control. Post-administration of 100 and 200 mg/kg b.w., LPME markedly (p > 0.05) reduced the intoxication and reversed the changes to normal level (Table 2).
Table 2

Effect of LPME on tissue protein and antioxidant enzymes in thyroid of rat

Treatment

Protein (μg/mg tissue)

CAT (U/min)

POD (U/min)

SOD (U/mg protein)

Control

0.57 ± 0.01++

2.88 ± 0.09++

8.0 ± 0.09++

26.17 ± 0.77++

DMSO + olive oil

0.53 ± 0.01 ++

2.90 ± 0.05++

8.2 ± 0.05++

25.0 ± 0.92++

20 mg/kg KBrO3

0.35 ± 0.09a

1.16 ± 0.08a

6.3 ± 0.20a

12.0 ± 0.08a

100 mg/kg LPME+ KBrO3

0.58 ± 0.03++

2.18 ± 0.04++

7.0 ± 0.29++

18.3 ± 0.60++

200 mg/kg LPME+ KBrO3

0.52 ± 0.01++

2.62 ± 0.03++

7.8 ± 0.04++

20.10 ± 1.19++

200 mg/kg LPME alone

0.58 ± 0.01++

2.93 ± 0.09++

8.19 ± 0.08++

28.0 ± 0.82++

Mean ± SE (n = 6 number)

aIndicate significance from the control group at P < 0.01 probability level

++ Indicate significance from the KBrO3 group at P < 0.01 probability level

Table 3 revealed the activities of phase II metabolizing enzymes viz.; GST, GSH-Px, GSR, QR, and γ-GT in various groups. KBrO3-treatment in rats significantly (p < 0.01) depleted the activity of GST, GSH-Px, GSR and QR, whereas increased the activity of γ-GT comparatively to control group. The modulation were significantly (p > 0.01) reversed by the co-treatment of 100 and 200 mg/kg b.w., LPME near to control group.
Table 3

Effect of LPME on thyroid GST, GSR, GSH-Px, γ-GT and QR activity in rat

Treatment

GSH-Px (nM/mg protein)

GSR (nM/min/mg protein)

GST(nM/min/mg protein)

γ-GT (nM/min/mg protein)

QR (nM/min/mg protein)

Control

103.3 ± 2.23++

70.7 ± 1.9++

41.7 ± 1.0++

49.3 ± 3.4++

92.7 ± 2.9++

DMSO + olive oil

102.7 ± 1.0++

69.3 ± 2.6++

41.3 ± 0.9++

49.7 ± 3.9++

91.2 ± 2.7++

20 mg/kg KBrO3

80.3 ± 2.7a

54.3 ± 2.1a

17.7 ± 1.1a

105.5 ± 1.7a

72.5 ± 3.5a

100 mg/kg LPME+ KBrO3

98.3 ± 1.0++

64.0 ± 2.9++

34.7 ± 1.9++

92.3 ± 2.2++

85.2 ± 3.3++

200 mg/kg LPME+ KBrO3

101.0 ± 0.7++

69.0 ± 1.9++

39.5 ± 0.7++

58.5 ± 1.4++

91.4 ± 2.5++

200 mg/kg LPME alone

104.7 ± 2.1++

71.7 ± 1.8++

41.5 ± 0.7++

50.3 ± 2.1++

94.6 ± 2.6++

Mean ± SE (n = 6 number)

aIndicate significance from the control group at P < 0.01 probability level

++ Indicate significance from the KBrO3 group at P < 0.01 probability level

TBARS, H2O2, GSH and tissue nitrite are key marker of lipid peroxidation and cellular oxidative stress. KBrO3 effects on the content of TBARS, H2O2, and GSH are shown in Table 4. Administration of 20 mg/kg b.w., of KBrO3 significantly (p < 0.01) reduced the concentrations of GSH while increased H2O2 and TBARS as compare to control. TBARS, tissue nitrite was significantly reduced (p < 0.01) by LPME decreased the level of TBARS at 100 and 200 mg/kg (p < 0.01) as compared to KBrO3 group. Level of GSH was improved while H2O2 was reduced (p < 0.01) by LPME at 100 mg/kg and 200 mg/kg b.w, respectively.
Table 4

Effect of LPME on thyroid GSH, TBARS, H2O2

Treatment

TBARS (nM/min/mg protein

GSH (μM/g tissue)

H2O2 (nM/min/mg tissue)

Control

12.8 ± 1.14++

0.44 ± 0.02++

0.86 ± 0.02++

DMSO + olive oil

13.0 ± 1.06++

0.44 ± 0.03++

0.85 ± 0.02++

20 mg/kg KBrO3

20.3 ± 0.71a

0.67 ± 0.01a

1.03 ± 0.01a

100 mg/kg LPME+ KBrO3

15.3 ± 1.35++

0.52 ± 0.04++

0.94 ± 0.03++

200 mg/kg LPME+ KBrO3

13.3 ± 0.95++

0.44 ± 0.05++

0.88 ± 0.03++

200 mg/kg LPME alone

12.0 ± 0.76++

0.40 ± 0.06++

0.82 ± 0.02++

Mean ± SE (n = 6 number)

aIndicate significance from the control group at P < 0.01 probability level

+, ++ Indicate significance from the KBrO3 group at P < 0.01 probability level

Thyroid weight and genotoxicity

Effects of LPME against KBrO3 administration on rats thyroid weight, relative tissue weight and % DNA fragmentation are shown in Table 5. KBrO3 caused a significant (p < 0.01) increased in thyroid tissue weight and relative thyroid tissue weight and %DNA damages as compared to non treated control group. Post-treatment of LPME erased the toxic effect of KBrO3 on rat and reduced the thyroid weight, relative tissue weight and % DNA fragmentation and significantly (p < 0.01) reversed towards control group.
Table 5

Effect of LPME on thyroid weight, relative thyroid weight and % DNA damages

Treatment

% DNA fragmentation

Thyroid. weight (g)

Relative thyroid weight (% to body weight)

Control

3.8 ± 2.3 ++

55.3 ± 2.7++

0.55 ± 0.02++

DMSO + olive oil

3.9 ± 2.1++

56.5 ± 2.2++

0.56 ± 0.03++

20 mg/kg KBrO3

30.4 ± 2.0a

79.7 ± 2.9a

0.79 ± 0.09a

100 mg/kg LPME+ KBrO3

7.2 ± 1.8 ++

67.8 ± 2.4++

0.67 ± 0.04++

200 mg/kg LPME+ KBrO3

4.4 ± 3.8++

57.3 ± 2.6++

0.57 ± 0.06++

200 mg/kg LPME alone

3.7 ± 2.6++

56.7 ± 2.2++

0.56 ± 0.02++

Mean ± SE (n = 6 number)

aIndicate significance from the control group at P < 0.01 probability level

++ Indicate significance from the KBrO3 group at P < 0.01 probability level

Histopathology of thyroid tissue

Microscopic examinations of various treated groups are shown in Table 6. Administration of KBrO3 caused colloid depletion and cellular hypertrophy, blood vessels congestion, inflammatory cells infiltrations and follicular shape disruptionand follicular cells hyperplasia. Post-treatment with LPME significantly erased the injuries near to control rats.
Table 6

Effect of LPME on thyroid histopathology

Treatment

Colloids depletion

Hyper-Trophy

Hyperplasia

Blood vessel congestion

Degeneration of follicular architecture

Control

DMSO + olive oil

20 mg/kg KBrO3

+++

+++

+++

+++

+++

100 mg/kg LPME+ KBrO3

−/+

−+

−/+

200 mg/kg LPME+ KBrO3

−+

200 mg/kg LPME alone

-, normal; −/+, mild; ++, medium; +++, severely damaged

Discussion

Thyroid hormones are essential for normal growth of organs, development, function and also regulate hepatocytes metabolism while liver in turn metabolizes thyroid hormones. It means that liver and thyroid hormones are connected with one another, dysfunction of one causes disturbance of other [17]. The hypothalamus releases thyrotrophic-releasing hormone (TRH), which stimulates pituitary gland to release thyroid stimulating hormone (TSH), which in turn promotes thyroid cells to produce thyroid hormones. When level of thyroid hormone is low than TSH and TRH are high, try to increase thyroid hormone and causes risk of thyroid tumor in rats [5]. Our results showed that administration of KBrO3 depleted the secretion of thyroid hormones i.e., T3 and T4 and elevated TSH level in serum of rats which was recovered by LPME. Similar results were reported by Hamidian et al., [7].

The present study revealed that marked changes were induced by KBrO3 in absolute b.w and % increase in body weight. KBrO3 treatment of rats significantly decreased the b.w, as compare to the non-treated control group. Our results are similar to the findings reported by Farombi et al. [4] that KBrO3 treatment to rat decreases the b.w non significantly as compare to control group. Other study also determined that that low amount of KBrO3 is not toxic as well as mutagenic (Yamaguchi et al., [29]. Increased lipid peroxidation and/or altered non-enzymatic and enzymatic antioxidant systems contributed oxidative stress. Various reports revealed that various enzymatic and non-enzymatic systems in mammalian cell have the capability to reduced ROS and other free radicals [25]. Toxicity induced with KBrO3 results from its metabolism through CYP 450 into free radicals that in turns leads to oxidative damages. In thyroid presence of cytochrome P450 enzyme system has not been established and injuries induced in thyroid are considered indirectly via the production of metabolites in other organs. In the present study induction of KBrO3 significantly alter the enzymatic level which was reversed by co-treatment of LPME. Similar reports were obtained by the exposure of KBrO3 in rats which has been restored by supplementation of Ficus racemosa and a natural antioxidant kolaviron [14]. Free radicals react with DNA to form a mutagenic pirimedopurinone adduct (M1G) of deoxyguanosine [18] causes genomic instability and damages. The data revealed that the treatment of KBrO3 causes significant oxidative DNA damage in thyroid tissue of rats which are reversed by LPME. Similar investigation was reported by Khan et al., [13] during study of protective effects of Digeramuricata. These results show that the extract contains bioactive phenolic and poly phenolic compounds which play important role in DNA repair. Data of the present study revealed that KBrO3 treatment in rats caused colloids depletion and hypertrophy, blood vessels congestion, follicular shape degradation and hyperplasia in thyroid. Treatment with LPME significantly erased the injuries. Similar observation was reported by Hooth et al. [8] during drinking water exposure of sodium chlorate in rats.

Abbreviations

GSR: 

Glutathione reductase

KBrO3

Potassium bromate

ROS: 

Reactive oxygen species

TRH: 

Thyrotrophic-releasing hormone

TSH: 

Thyroid stimulating hormone

Declarations

Acknowledgements

We thankful to all my friends and college who guided me.

Funding

No funding is received for conduction of the study.

Availability of data and materials

Data and material will be available as per Journal rule.

Authors’ contributions

RAK (ORCID ID: 0000–0003–0453-2090) completed experimentations and analysis of data as well as considerable influence to outset and design, analysis of data and drafting of manuscript.

Ethics approval and consent to participate

The study was conducted according to the protocol approved by ethical committee of the University.

Consent for publication

All the authors are agreeing to submit the paper in your esteemed Journal.

Competing interests

The author declares that he/she has no competing interests.

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Authors’ Affiliations

(1)
Department of Biotechnology, Faculty of Biological Sciences, University of Science and Technology

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Copyright

© The Author(s). 2017

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