BioMed Research International

Volume 2014 (2014), Article ID 590897, 12 pages

http://dx.doi.org/10.1155/2014/590897

Research Article

Supplementation of T₃ Recovers Hypothyroid Rat Liver Cells from Oxidatively Damaged Inner Mitochondrial Membrane Leading to Apoptosis

Sutapa Mukherjee,1,2 Luna Samanta,1,3 Anita Roy,⁴ Shravani Bhanja,⁴ and Gagan B. N. Chainy1,4

¹Department of Zoology, Utkal University, Bhubaneswar, Odisha 751004, India

²Department of Zoology, Visva-Bharati (A Central University), Santiniketan, West Bengal 731235, India

³Department of Zoology, Ravenshaw University, Cuttack, Odisha 753003, India

⁴Department of Biotechnology, Utkal University, Bhubaneswar, Odisha 751004, India

Received 28 February 2014; Accepted 9 May 2014; Published 28 May 2014

Academic Editor: Kim Bridle

Copyright © 2014 Sutapa Mukherjee et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Hypothyroidism is a growing medical concern. There are conflicting reports regarding the mechanism of oxidative stress in hypothyroidism. Mitochondrial oxidative stress is pivotal to thyroid dysfunction. The present study aimed to delineate the effects of hepatic inner mitochondrial membrane dysfunction as a consequence of 6-n-propyl-2-thiouracil-induced hypothyroidism in rats. Increased oxidative stress predominance in the submitochondrial particles (SMP) and altered antioxidant defenses in the mitochondrial matrix fraction correlated with hepatocyte apoptosis. In order to check whether the effects caused by hypothyroidism are reversed by T₃, the above parameters were evaluated in a subset of T₃-treated hypothyroid rats. Complex I activity was inhibited in hypothyroid SMP, whereas T₃ supplementation upregulated electron transport chain complexes. Higher mitochondrial H₂O₂ levels in hypothyroidism due to reduced matrix GPx activity culminated in severe oxidative damage to membrane lipids. SMP and matrix proteins were stabilised in hypothyroidism but exhibited increased carbonylation after T₃ administration. Glutathione content was higher in both. Hepatocyte apoptosis was evident in hypothyroid liver sections; T₃ administration, on the other hand, exerted antiapoptotic and proproliferative effects. Hence, thyroid hormone level critically regulates functional integrity of hepatic mitochondria; hypothyroidism injures mitochondrial membrane lipids leading to hepatocyte apoptosis, which is substantially recovered upon T₃ supplementation.

1. Introduction

Mitochondria, the powerhouses of eukaryotic cells, are instrumental in regulating the various signaling pathways involved in cell survival and death. The electron transport chain, localized in the inner membrane of mitochondrion, is the major source of intracellular reactive oxygen species (ROS), which renders the mitochondrion itself a highly vulnerable target [1, 2]. The mitochondrial oxidative stress has long been implicated in the aging process and in the pathogenesis of several human diseases, including cancer, neurodegenerative disorders, and thyroid dysfunction.

Thyroid hormones have profound impact upon mitochondrial biogenesis and activity [3, 4]. Hypothyroidism is known to diminish oxygen consumption and promote low metabolism causing disturbances in hemodynamic, cardiac, and renal functions [5]. The electron transport chain complexes and -ATPase activities are decreased in many tissues in thyroid deficient condition [6]. In fact, hypothyroid status was proposed as useful model to understand the molecular mechanisms involved in ischemia reperfusion, regulation of vascular function, and intravascular metabolism of lipoproteins [5]. Liver is well recognised as a major target organ for thyroid hormone [7]. In this perspective, studies on hepatic mitochondrial metabolism and functional integrity in thyroid dysfunction attain utmost relevance.

Previous reports have established significant modulation of various aspects of ROS metabolism and antioxidant defenses in the liver by experimentally induced hypo- and hyperthyroidism [8–10]. However, these reports were confined to whole mitochondrial fraction isolated from rat liver. We earlier delineated the mitochondrial effects, in particular, by reporting the influence of acute treatment of euthyroid rats with 3,5,3′-triiodo-L-thyronine () upon hepatic ROS generation, glutathione (GSH) redox status, and protein oxidation following time kinetics, after subfractionating mitochondria into submitochondrial particles (SMP) and matrix fraction [11]. As an extension to this, we presently elucidate the effect of 6-n-propyl-2-thiouracil- (PTU-) induced hypothyroidism upon various relevant prooxidative and antioxidative parameters in adult rat liver SMP and mitochondrial matrix fraction along with histological and apoptosis analyses. In order to check whether the effects caused by hypothyroidism are reversed by , the above parameters were evaluated in a subset of hypothyroid rats administered with . Following similar experimental regimen, we earlier found that hypothyroid state inflicted changes in intramitochondrial protein and nonprotein thiol redox status in rat testes that could not be fully reversed when was given to the hypothyroid rats [12]. It is opined that the present investigation in the light of our above-mentioned reports would enable comprehensive understanding as to how these important oxidative stress parameters are regulated in distinctive hepatic mitochondrial compartments in hypothyroidism, as to whether these are reversed by , and, if yes, as to what extent the damage is ameliorated.

2. Materials and Methods

2.1. Animals and Treatments

In the present experiment, liver tissues from rats of our earlier reported study were used [12]. The treatment regimen of the investigation is reported in brief. Six-month-old adult male Wistar rats (Rattus norvegicus) were obtained from the National Institute of Nutrition (Hyderabad, India) and housed in the Animal Room of the department at °C. Animals were randomly assorted into three groups, each containing five animals. Group I (euthyroid) rats were fed with standard diet and drinking water ad libitum. Group II (hypothyroid) rats were treated with 0.05% (w/v) PTU in drinking water for six weeks. After completion of this time period, administration of PTU was stopped and rats were given one daily injection of 0.01 N NaOH, i.p. (vehicle for ), for three consecutive days. Group III (hypothyroid+) rats were treated with 0.05% (w/v) PTU in drinking water for six weeks. After completion of this time period, administration of PTU was stopped and rats were given one daily injection of (20 μg/100 g body mass in 0.01 N NaOH, i.p.) for three consecutive days. Animal care, maintenance, and experiments were done under the supervision of the Institutional Animal Ethics Committee (IAEC) regulated by the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), Government of India. All the chemicals used were analytical grade.

2.2. Tissue Processing and Isolation of Submitochondrial Fractions

Rats were sacrificed under ether anesthesia. Liver was perfused with cold 0.9% (w/v) NaCl in order to remove blood as it might interfere with the assays. The tissue was properly cleaned, freed of connective tissues, pat dried on filter paper, weighed, and stored at −80°C till further analyses. All isolation procedures were carried out at 4°C. Submitochondrial fractionation of rat liver was done as mentioned previously [11]. Protein concentration of samples was estimated following the Biuret method using bovine serum albumin as standard.

2.3. Evaluation of Oxidative Damages to Mitochondrial Membrane Lipids

To determine membrane lipid peroxidation (LPx), the formation of thiobarbituric acid-reactive substances (TBARS) was monitored in SMP in the presence of 0.02% (w/v) butylated hydroxytoluene to suppress artifactual peroxidation during heating [13]. Besides endogenous LPx, susceptibility of SMP to oxidants was assessed in vitro. For this, SMP prepared from different groups of rats were incubated without any oxidant, with H₂O₂ (600 nmol/mg protein) and tert-butyl hydroperoxide (600 nmol/mg protein), respectively, for 1 h at 37°C prior to TBARS determination. Only sample incubated in buffer and not exposed to any oxidant was taken as control for each set.

2.4. Evaluation of Oxidative Damages to Mitochondrial Proteins

Protein carbonyl content was estimated in SMP and mitochondrial matrix fraction by detecting the reaction of dinitrophenylhydrazine with protein carbonyls to form protein hydrazones [14].

2.5. Evaluation of Mitochondrial ROS and ROS-Metabolizing Antioxidant Enzyme (AOE) Activities

The rate of superoxide radical () generation by SMP was measured as superoxide dismutase- (SOD-) inhibitable reduction of nitroblue tetrazolium (NBT) [11]. H₂O₂ content was determined in mitochondrial fraction following horseradish peroxidase-dependent oxidation of phenol red [15]. For estimating AOE activities, one milliliter of freeze-thawed mitochondrial matrix fraction was passed through 5 mL column of Sephadex G-25 in order to get rid of any interfering low molecular weight compounds. One unit of SOD activity was defined as the amount of enzyme capable of inhibiting 50% of nitrite formation under assay conditions [16]. Glutathione peroxidase (GPx) activity was assayed by measuring the rate of oxidation of NADPH in presence of hydroperoxide, reduced glutathione and glutathione reductase (GR) [17]. Total GPx activity was measured using cumene hydroperoxide as substrate whereas Se-dependent GPx was determined using tert-butyl hydroperoxide as substrate [18]. Activity of Se-independent GPx was obtained by subtracting the activity of Se-dependent GPx from that of total GPx.

2.6. Evaluation of Mitochondrial Protein-Bound and Nonprotein-Bound Thiol Content

For measuring protein-SH content, SMP and matrix samples were first precipitated in ice-cold 5% trichloroacetic acid (TCA) containing 0.01 N HCl and centrifuged at 1000 ×g for 15 min. Protein precipitates dissolved in 8 M guanidine hydrochloride were used to measure P-SH content, while nonprotein-SH content was estimated in TCA-treated matrix supernatants using 5,5′-dithiobis-2-nitrobenzoic acid [19, 20].

2.7. Evaluation of Functional Activity of Inner Mitochondrial Membrane

The activities of the mitochondrial inner membrane-associated respiratory chain enzyme complexes were assayed in SMP as detailed previously [11].

2.8. Histological Analyses

Following sacrifice, liver tissues were immediately fixed for histological analyses in freshly prepared sublimate formol, dehydrated in graded ethanol series, cleared in xylene, and embedded in paraffin wax. Tissues were sectioned at 5 μm and the sections were stained with hematoxylin and eosin. The sections were observed under light microscope. The tissue sections were analysed by a histologist who was not aware of sample assignment to the experimental groups.

2.9. Detection of Apoptosis

Histochemical detection of apoptosis was performed in tissue sections prepared from liver of euthyroid, hypothyroid, and hypothyroid + rats by terminal deoxynucleotidyl transferase- (TdT-) mediated dUTP-biotin nick end labeling (TUNEL) assay. Specific staining for in situ apoptosis was performed using TACS in situ Apoptosis Detection Kit (R&D Systems Inc., Minneapolis, USA) following the manufacturer’s protocol. TUNEL positive cells were taken as the cells that were stained intense brown.

2.10. Statistical Analysis

Data were subjected to two-way analysis of variance followed by Duncan’s new multiple range test to determine the level of significance between control and treatment means. Data were presented as mean values ± S.D. and differences between groups were considered statistically significant at the minimal level of .

3. Results

3.1. Oxidative Damages to Mitochondrial Membrane Lipids

Endogenous membrane LPx expressed in terms of TBARS level was significantly enhanced (20.89%, ) in SMP from hypothyroid rats compared to euthyroid (Figure 1(a)). Treatment of hypothyroid rats with reduced TBARS level from that of hypothyroid rats but could not reach the basal value. Determination of TBARS level after in vitro incubation with oxidants revealed that hypothyroid SMP were the most susceptible to peroxidation induced by both H₂O₂ and tert-butyl hydroperoxide which subsided to certain extent after treatment (Figure 1(b)).

(a)

(b)

Figure 1: Effect of PTU-induced hypothyroidism and its reversal by upon oxidative damage to mitochondrial membrane lipids. (a) Endogenous membrane lipid peroxidation (TBARS formed) in submitochondrial particles (SMP) isolated from liver of rats. (b) In vitro oxidant-induced TBARS level for which SMP were incubated without any oxidant and with H₂O₂ (600 nmol/mg protein) and tert-butyl hydroperoxide (600 nmol/mg protein), respectively, for 1 h at 37°C prior to TBARS determination. Data are means ± S.D. of five animals/group. Statistical significance is denoted by , , and compared to euthyroid rats; compared to hypothyroid rats.

3.2. Oxidative Damages to Mitochondrial Proteins

Hypothyroidism caused significant reduction in protein carbonyl content in SMP (43.87%, ), whereas administration of resulted in 1.5-fold elevation compared to euthyroid (Figure 2(a)). Similar was the trend in mitochondrial matrix where hypothyroid rats showed decreased protein carbonylation (62.38%, ) whereas hypothyroid + rats recorded almost two-fold augmentation (Figure 2(b)).

(a)

(b)

Figure 2: Effect of PTU-induced hypothyroidism and its reversal by upon oxidative damage to mitochondrial proteins. (a) Protein carbonyl content in submitochondrial particles. (b) Protein carbonyl content in mitochondrial matrix fraction isolated from liver of rats. Data are means ± S.D. of five animals/group. Statistical significance is denoted by compared to euthyroid rats; compared to hypothyroid rats.

3.3. Mitochondrial ROS and ROS-Metabolizing AOE Activities

SOD-sensitive -mediated NBT reduction was significantly increased by 58.11% () in hypothyroid + rats (Figure 3(a)). The activity of matrix SOD was significantly enhanced (64.16%, ) in -treated hypothyroid rats whereas hypothyroid rats did not record any significant change (Figure 3(b)). Hypothyroid rats exhibited almost 1.8-fold increase in H₂O₂ content from euthyroid (Figure 4(a)). On the other hand, hypothyroid + T₃ rats showed H₂O₂ content close to basal level. While hypothyroid rats showed no change in Se-dependent GPx activity, subsequent treatment with T₃ decreased enzymatic activity significantly (40%, ) (Figure 4(b)). The trend was quite different in case of Se-independent GPx activity which was significantly downregulated in hypothyroid rats (63.33%, ), whereas treatment induced the enzyme activity albeit still lesser than euthyroid (Figure 4(c)).

(a)

(b)

Figure 3: Effect of PTU-induced hypothyroidism and its reversal by upon mitochondrial ROS and ROS-metabolizing enzymes. (a) Superoxide radical generation capacity of submitochondrial particles. (b) Superoxide dismutase activity in the mitochondrial matrix fraction isolated from liver of rats. Data are means ± S.D. of five animals/group. Statistical significance is denoted by and compared to euthyroid rats; compared to hypothyroid rats.

(a)

(b)

(c)

Figure 4: Effect of PTU-induced hypothyroidism and its reversal by upon mitochondrial ROS and ROS-metabolizing enzymes. (a) Hydrogen peroxide content. (b) Se-dependent glutathione peroxidase (GPx) activity. (c) Se-independent GPx activity in the mitochondrial matrix fraction isolated from liver of rats. Data are means ± S.D. of five animals/group. Statistical significance is denoted by and compared to euthyroid rats; compared to hypothyroid rats.

3.4. Mitochondrial Protein-Bound and Nonprotein-Bound Thiol Content

Protein-SH content was significantly enhanced in SMP and mitochondrial matrix fraction of hypothyroid rats with regard to euthyroid (Figures 5(a) and 5(b)). While administration of to hypothyroid rats enhanced protein-SH content in SMP (35.82%, ), it lowered the value to basal level in mitochondrial matrix. The nonprotein thiol content was increased significantly in both the treated groups (Figure 5(c)).

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(b)

(c)

Figure 5: Effect of PTU-induced hypothyroidism and its reversal by upon mitochondrial thiol content. (a) Protein-bound thiol content in submitochondrial particles. (b) Protein-bound thiol content in mitochondrial matrix fraction. (c) Nonprotein thiol content in mitochondrial matrix fraction isolated from liver of rats. Data are means ± S.D. of five animals/group. Statistical significance is denoted by , , and compared to euthyroid rats; compared to hypothyroid rats.

3.5. Functional Activity of Inner Mitochondrial Membrane

NADH:duroquinone oxidoreductase activity was reduced by 15.18% () in the hypothyroid rats. However, administration of to hypothyroid rats resulted in 22.05% () increment over euthyroid (Figure 6(a)). Succinate:DCPIP oxidoreductase activity was not affected significantly by hypothyroid condition. However, treatment of hypothyroid rats with caused 26.28% () enhancement in enzymatic activity (Figure 6(b)). Administration of caused 2.7-fold increase in succinate:cytochrome c oxidoreductase activity (Figure 6(c)). ATPase activity was significantly enhanced () in hypothyroid rats administered with (Figure 6(d)).

(a)

(b)

(c)

(d)

Figure 6: Effect of PTU-induced hypothyroidism and its reversal by upon mitochondrial membrane-bound respiratory enzyme complexes. (a) NADH:duroquinone (DQ) oxidoreductase activity. (b) Succinate:2,6-dichlorophenolindophenol (DCPIP) oxidoreductase activity. (c) Succinate:cytochrome c oxidoreductase activity. (d) ATPase activity in the submitochondrial particles isolated from liver of rats. Data are means ± S.D. of five animals/group. Statistical significance is denoted by , , and compared to euthyroid rats; and compared to hypothyroid rats.

3.6. Histological Analyses and Detection of Apoptosis

Euthyroid animals displayed normal histoarchitecture of rat liver. However, liver sections from hypothyroid rats showed marked reduction in the number of cells apart from disappearance and disintegration of the nuclei in several cells. On the other hand, administration of to hypothyroid rats clearly revealed hepatocyte proliferation (Figures 7(a)–7(c)). Liver sections from hypothyroid rats exhibited considerable presence of TUNEL positive cells, indicating onset of apoptosis (Figures 8(a)–8(c)). However, hypothyroid + rats showed opposite effect since the sections responded negatively to the TUNEL assay.

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Figure 7: Photomicrographs of transverse sections of liver from (a) euthyroid rats, (b) hypothyroid rats, and (c) hypothyroid + rats. Haematoxylin and eosin stain (400x).

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(b)

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Figure 8: Photomicrographs of transverse sections of liver from (a) euthyroid rats, (b) hypothyroid rats, and (c) hypothyroid + rats showing the results of TUNEL assay at 400x.

4. Discussion

Hypothyroidism is known to decrease mitochondrial oxygen consumption and ATP synthesis [21] while injection of T₃ increases oxygen consumption and metabolic rate [22]. It was later revealed that mitochondrial production of ROS mostly occurs during state IV respiration [23], particularly in the proximity of complex I and complex III of the electron transport chain [24]. Presently, the analyses of the activities of mitochondrial inner membrane-bound enzyme complexes involved in cellular respiration revealed certain interesting aspects. Hypothyroid condition did not alter activities of respiratory chain complexes except that it had a strong influence on NADH-DQ oxidoreductase activity which was significantly downregulated. In stark contrast, supplemented hypothyroid rats exhibited substantially increased activities of all enzyme complexes in liver SMP. Unfortunately, cytochrome c oxidase activity could not be estimated in this study. It was earlier reported that mRNAs and protein levels of subunits of cytochrome c oxidase in liver were downregulated or unaffected in hypothyroid state, but, after thyroid hormone treatment, the levels of gene products increased rapidly reaching supranormal levels [25]. In fact, injection of into euthyroid rats accentuated activities of respiratory chain complexes in liver mitochondrial fraction [26] and SMP [11]. It is apparent from this study that although induction of hypothyroidism did not register any significant change in ATPase activity, subsequent treatment with caused significant enhancement. Vacca et al. [27] reported impaired transport of phosphate and adenine nucleotide across the inner mitochondrial membrane in hypothyroidism that was accompanied with decreased gene expression of adenine nucleotide translocase. Therefore, while upregulates all the respiratory chain complexes of inner mitochondrial membrane accounting for enhanced oxygen consumption and metabolic rate, complex I is a vulnerable target in hypothyroid condition. This is substantiated by the fact that hypothyroid phenotype is contributed by mitochondrial complex I inactivation due to translocated neuronal nitric oxide synthase [28]. Nevertheless, in both the altered thyroid states, electron leakage and generation of ROS are an unavoidable consequence.

We measured generation capacity of inner mitochondrial membrane using SMP that are devoid of SOD. -induced increase in generation is well known [11, 29, 30]. SOD is the primary AOE that dismutates . Mitochondrial matrix contains MnSOD which is encoded by nuclear gene. Its activity was recorded to be high in response to treatment. This is accounted by the fact that can upregulate MnSOD expression through NF-κB activation [31]. Mitochondria are effective sources of H₂O₂ primarily through SOD and outer membrane enzyme monoamine oxidase. Besides, H₂O₂ is generated in cytosol by several oxidases. Since H₂O₂ can easily traverse membranes and can access distant sites, therefore, we performed H₂O₂ assay in mitochondrial fraction in order to get an idea about total mitochondrial H₂O₂ content. Higher H₂O₂ levels in hypothyroid mitochondria could arise due to ineffective function of H₂O₂-metabolizing AOEs as reflected in diminished total GPx activity. When GPx isoenzyme activities in response to treatment were analyzed, it was observed that Se-independent GPx activity was reduced in response to hypothyroidism but was enhanced when challenged with . On the contrary, Se-dependent GPx activity was significantly reduced when hypothyroid rats were challenged with . Thus, these results clearly establish a differential regulatory influence of on expression of different isoenzymes of GPx.

Both oxygen consumption and free radical production take place in mitochondrial inner membrane. The sensitivity of these membranes to oxidative damage is strongly dependent on their unsaturated fatty acid content. The lipid environment can directly affect membrane function, including mitochondrial electron transport and ROS production [32]. Available data on lipid peroxidative processes and oxidative status in hypothyroid liver are controversial. It was reported that levels of LPx products in liver from hypothyroid rats [33] and mice [21] do not differ from euthyroid values. On the other hand, Mogulkoc et al. [34] reported reduced MDA level in hepatic tissue from hypothyroid rats. It was asserted that hypothyroidism provided protection against LPx [35]. It further prevented increase in LPx as well as tissue damage induced by intracolonic administration of trinitrobenzene sulfonic acid and decreased susceptibility to oxygen radical-induced lung damage in newborn rats exposed to prolonged hyperoxia [36, 37]. The lower toxicity of arsenic in hypothyroid animals was associated with prevention of arsenic-induced LPx in liver and kidneys [38]. Furthermore, hypothyroidism was able to protect against acetaminophen hepatotoxicity [39]. Serum TBARS concentration did not show differences between euthyroid, overt hypothyroid, and subclinical hypothyroid women [40]. On the contrary, hypothyroidism did not provide protection from LPx in testicular mitochondria as evident from augmented TBARS levels in SMP [12]. There is also evidence of increased LPx in erythrocytes, heart, and plasma of PTU-treated rats [41, 42] and serum of hypothyroid patients [43–45]. In conformity with this, the present study revealed greater extent of mitochondrial membrane lipid damage in hypothyroidism which was alleviated upon treatment. A similar adaptive response was reported in hyperthyroid mice arising from decreased fatty acid unsaturation index [21]. In a study in hypothyroid patients before and after treatment, Baskol et al. [46] reported that MDA levels were higher in patients with hypothyroidism before treatment, which subsided after thyroxine replacement. It seems that lack of effective antioxidant protection as well as possible prooxidant activities could explain the higher than normal LPx levels. Se-independent GPx is known to catalyze GSH-dependent reduction of phospholipid hydroperoxides in situ in biological membranes [47], and its overexpression in cells attenuates LPx under normal condition as well as during oxidative stress. Thus, reduction in Se-independent GPx activity in hypothyroid rats might be the reason for observing significantly high TBARS level as well. Although injection of induced the activity, it could not restore the normal level. These data clearly establish the pivotal role essayed by Se-independent GPx in maintaining mitochondrial membrane integrity in thyroid dysfunction.

Quite intriguingly, our results indicate that hypothyroid state is accompanied with general decrease in oxidatively damaged mitochondrial proteins. Although lipid peroxidation end products such as malondialdehyde and 4-hydroxynonenal are known to initiate carbonylation of proteins, yet these parameters may not always be correlating with each other. It is important to consider that the steady state level of proteins in cells is dependent on both synthesis and degradation, that is, metabolic turnover. Accumulation of altered proteins in tissues can be either due to a higher rate of oxidation and other types of modifications, due to a lower rate of degradation of the modified proteins, or due to both. Oxidative modification of a protein makes it more susceptible to proteolysis largely due to the unfolding of the targeted protein domains. Unfolding results in an increased exposure of hydrophobic residues that are normally hidden in the interior of soluble proteins and such hydrophobic patches are known to favour recognition and degradation by the proteasome and the Lon protease [48, 49]. In addition, lipid oxidation is the primary event following oxidative stress, whereas protein carbonylation occurs secondarily. On the other hand, hypothyroid + rats showed higher index of oxidative damage to proteins in both SMP and matrix fractions. Significantly higher protein hydrazone derivatives were seen in these rats. Stability of protein-SH groups was also adversely affected in the mitochondrial matrix fraction. This provides definitive evidence that renders the proteins of the mitochondrial subcompartments more vulnerable to oxidative damage and the utilization of ROS in lipid and protein oxidation of SMP is reciprocal in altered thyroid states.

Glutathione (GSH), the most predominant nonprotein thiol, is involved in many biological activities including neutralization of ROS, detoxification of xenobiotics, and maintenance of SH level in proteins [50]. Effect of hypothyroidism on hepatic GSH is controversial. As observed presently, increased nonprotein thiol content in hypothyroid condition or in case of supplementation might be an adaptive response to protect mitochondria against oxidative damage. In fact, is known to trigger GSH biosynthesis [51]. However, in hypothyroid condition, GR activation contributes to the GSH pool by rapid conversion of GSSG into GSH. Increased protein-SH signifies proteins to be in their native state while its decrease suggests oxidative predominance.

Histological analyses of liver samples interestingly showed recovery of cellular integrity in hypothyroid rats supplemented with . This finding is well justified by the fact that powerfully induced hepatocytes to enter S phase 24 h after injection [52]. -induced cyclin D1 expression enhanced phosphorylation of pRb and increased expression of transcription factor E2F mediated hepatocyte proliferation [53]. Besides, Alisi et al. [54] found that, both in control and in partially hepatectomized animals, hyperthyroidism increased cyclins D1, E, and A levels and the activity of cyclin-cdk complexes and decreased the levels of cdk inhibitors such as p16 and p27. These authors further showed that hypothyroidism caused downregulation of the activity of cyclin-cdk complexes decreasing cyclin levels. Thus, exerts proproliferative effects on liver cells by regulating cell cycle proteins.

Morphological hallmarks of apoptosis in the nucleus are chromatin condensation and nuclear fragmentation [55]. The condensation starts peripherally along the nuclear membrane, forming a crescent or ring-like structure. During later stages of apoptosis the nucleus further condenses, and finally it breaks up inside a cell with an intact cell membrane, a feature described as karyorrhexis [56]. DNA strand breaks can be detected by incorporating labeled dUTP by the TUNEL method. The presence of apoptotic cells in hypothyroid liver sections as revealed from TUNEL assay clearly indicates activation of apoptotic pathways, which was later reversed upon administration of . It is suggested that hypothyroidism-induced cytochrome c release to cytosol during early development might contribute to initiation of apoptosis through formation of apoptosomes and activation of caspase cascade. Moreover, congenital hypothyroidism increased not only the extent but also the duration of apoptosis following similar mitochondrial mechanism in hippocampal neurons of developing rats [57]. The antiapoptotic effects of are well supported by both in vivo and in vitro reports. Fernández et al. [31] showed that administration of 0.1 mg /kg body weight for 68–72 h caused upregulation in expression of the antiapoptotic protein Bcl-2. inhibited TNFα/Fas-induced apoptosis in mouse hepatocytes [58]. It is relevant to mention in this context that protected cardiac myocytes against ischemia-induced apoptosis via Akt signaling [59]. Thus, can initiate hepatoprotective mechanism in pathological conditions by suppressing apoptosis and enabling hepatocyte survival.

5. Conclusion

It is apparent from the above data that hypothyroidism brought about metabolic suppression antagonistic to the hypermetabolic state induced by , yet it inflicted considerable cellular injury primarily through oxidative damage to mitochondrial membrane lipids and inhibition of the electron transport chain complex I. Hydroperoxide neutralization was severely affected in hypothyroidism and the compromised antioxidant defenses failed to contain the high levels of ROS. Accumulation of ROS and loss of membrane integrity are the two primary factors that potentially trigger apoptosis. However, treatment exerted antiapoptotic and proproliferative effects on hypothyroid liver cells. Nevertheless, mitochondrial membrane and matrix proteins seemed more vulnerable in hyperthyroid state, which also disturbed the mitochondrial oxidant  :  antioxidant balance. Quite aptly, a recent clinical study suggested that antioxidant therapy should be advised along with thyroid hormone replacement therapy to diminish further complications [60]. Taken together, these data confirm that hypothyroidism-induced severe hepatocellular injury can be substantially recovered upon T₃ supplementation.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors thank the Heads of the Departments of Zoology and Biotechnology (supported by the Department of Biotechnology, Government of India), Utkal University, for providing necessary facilities during the experiment. Sutapa Mukherjee is grateful to CSIR, New Delhi, for financial assistance. The cooperation of the Director of Institute of Life Sciences, Bhubaneswar, for providing ultracentrifugation facility is deeply acknowledged.

References

J. F. Turrens, “Mitochondrial formation of reactive oxygen species,” Journal of Physiology, vol. 552, no. 2, pp. 335–344, 2003.

M. P. Murphy, “How mitochondria produce reactive oxygen species,” Biochemical Journal, vol. 417, no. 1, pp. 1–13, 2009.

C. Wrutniak-Cabello, F. Casas, and G. Cabello, “Thyroid hormone action in mitochondria,” Journal of Molecular Endocrinology, vol. 26, no. 1, pp. 67–77, 2001.

J. M. Weitzel, K. A. H. Iwen, and H. J. Seitz, “Regulation of mitochondrial biogenesis by thyroid hormone,” Experimental Physiology, vol. 88, no. 1, pp. 121–128, 2003.

M. Franco, E. Chavez, and O. Perez-Mendez, “Pleiotropic effects of thyroid hormones: learning from hypothyroidism,” Journal of Thyroid Research, vol. 2011, Article ID 321030, 17 pages, 2011.

J. Kvetny, L. Wilms, P. L. Pedersen, and J. Larsen, “Subclinical hypothyroidism affects mitochondrial function,” Hormone and Metabolic Research, vol. 42, no. 5, pp. 324–327, 2010.

X. Feng, Y. Jiang, P. Meltzer, and P. M. Yen, “Thyroid hormone regulation of hepatic genes in vivo detected by complementary DNA microarray,” Molecular Endocrinology, vol. 14, no. 7, pp. 947–955, 2000.

K. Das and G. B. N. Chainy, “Modulation of rat liver mitochondrial antioxidant defence system by thyroid hormone,” Biochimica et Biophysica Acta, vol. 1537, no. 1, pp. 1–13, 2001.

P. Venditti, R. de Rosa, and S. di Meo, “Effect of thyroid state on H₂O₂ production by rat liver mitochondria,” Molecular and Cellular Endocrinology, vol. 205, no. 1-2, pp. 185–192, 2003.

P. Venditti, R. de Rosa, and S. di Meo, “Effect of thyroid state on susceptibility to oxidants and swelling of mitochondria from rat tissues,” Free Radical Biology and Medicine, vol. 35, no. 5, pp. 485–494, 2003.

S. Chattopadhyay, D. K. Sahoo, A. Roy, L. Samanta, and G. B. N. Chainy, “Thiol redox status critically influences mitochondrial response to thyroid hormone-induced hepatic oxidative injury: a temporal analysis,” Cell Biochemistry and Function, vol. 28, no. 2, pp. 126–134, 2010.

S. Chattopadhyay, S. Choudhury, A. Roy, G. B. N. Chainy, and L. Samanta, “T₃ fails to restore mitochondrial thiol redox status altered by experimental hypothyroidism in rat testis,” General and Comparative Endocrinology, vol. 169, no. 1, pp. 39–47, 2010.

H. Ohkawa, N. Ohishi, and K. Yagi, “Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction,” Analytical Biochemistry, vol. 95, no. 2, pp. 351–358, 1979.

R. L. Levine, D. Garland, C. N. Oliver et al., “Determination of carbonyl content in oxidatively modified proteins,” Methods in Enzymology, vol. 186, pp. 464–478, 1990.

E. Pick and Y. Keisari, “Superoxide anion and hydrogen peroxide production by chemically elicited peritoneal macrophages—induction by multiple nonphagocytic stimuli,” Cellular Immunology, vol. 59, no. 2, pp. 301–318, 1981.

K. Das, L. Samanta, and G. B. N. Chainy, “A modified spectrophotometric assay of superoxide dismutase using nitrite formation by superoxide radicals,” Indian Journal of Biochemistry and Biophysics, vol. 37, no. 3, pp. 201–204, 2000.

D. E. Paglia and W. N. Valentine, “Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase,” The Journal of Laboratory and Clinical Medicine, vol. 70, no. 1, pp. 158–169, 1967.

F. Carmagnol, P. M. Sinet, and H. Jerome, “Selenium-dependent and non-selenium-dependent glutathione peroxidases in human tissue extracts,” Biochimica et Biophysica Acta, vol. 759, no. 1-2, pp. 49–57, 1983.

J. Sedlak and R. H. Lindsay, “Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent,” Analytical Biochemistry, vol. 25, no. 1, pp. 192–205, 1968.

J. Wudarczyk, G. Debska, and E. Lenartowicz, “Relation between the activities reducing disulfides and the protection against membrane permeability transition in rat liver mitochondria,” Archives of Biochemistry and Biophysics, vol. 327, no. 2, pp. 215–221, 1996.

F. Guerrieri, M. Kalous, E. Adorisio et al., “Hypothyroidism leads to a decreased expression of mitochondrial F0F1- ATP synthase in rat liver,” Journal of Bioenergetics and Biomembranes, vol. 30, no. 3, pp. 269–276, 1998.

M. Moreno, A. Lanni, A. Lombardi, and F. Goglia, “How the thyroid controls metabolism in the rat: different roles for triiodothyronine and diiodothyronines,” Journal of Physiology, vol. 505, no. 2, pp. 529–538, 1997.

B. Chance, H. Sies, and A. Boveris, “Hydroperoxide metabolism in mammalian organs,” Physiological Reviews, vol. 59, no. 3, pp. 527–605, 1979.

A. Y. Andreyev, Y. E. Kushnareva, and A. A. Starkov, “Mitochondrial metabolism of reactive oxygen species,” Biochemistry (Moscow), vol. 70, no. 2, pp. 200–214, 2005.

R. J. Wiesner, T. T. Kurowski, and R. Zak, “Regulation by thyroid hormone of nuclear and mitochondrial genes encoding subunits of cytochrome-c oxidase in rat liver and skeletal muscle,” Molecular Endocrinology, vol. 6, no. 9, pp. 1458–1467, 1992.

P. Venditti, R. Pamplona, M. Portero-Otin, R. de Rosa, and S. di Meo, “Effect of experimental and cold exposure induced hyperthyroidism on H₂O₂ production and susceptibility to oxidative stress of rat liver mitochondria,” Archives of Biochemistry and Biophysics, vol. 447, no. 1, pp. 11–22, 2006.

R. A. Vacca, L. Moro, G. Caraccio, F. Guerrieri, E. Marra, and M. Greco, “Thyroid hormone administration to hypothyroid rats restores the mitochondrial membrane permeability properties,” Endocrinology, vol. 144, no. 9, pp. 3783–3788, 2003.

M. C. Franco, V. G. Antico Arciuch, J. G. Peralta et al., “Hypothyroid phenotype is contributed by mitochondrial complex I inactivation due to translocated neuronal nitric-oxide synthase,” The Journal of Biological Chemistry, vol. 281, no. 8, pp. 4779–4786, 2006.

V. Fernández and L. A. Videla, “Influence of hyperthyroidism on superoxide radical and hydrogen peroxide production by rat liver submitochondrial particles,” Free radical research communications, vol. 18, no. 6, pp. 329–335, 1993.

P. Cornejo, G. Tapia, S. Puntarulo, M. Galleano, L. A. Videla, and V. Fernández, “Iron-induced changes in nitric oxide and superoxide radical generation in rat liver after lindane or thyroid hormone treatment,” Toxicology Letters, vol. 119, no. 2, pp. 87–93, 2001.

V. Fernández, G. Tapia, P. Varela et al., “Redox up-regulated expression of rat liver manganese superoxide dismutase and Bcl-2 by thyroid hormone is associated with inhibitor of κB-α phosphorylation and nuclear factor-κB activation,” Journal of Endocrinology, vol. 186, no. 3, pp. 539–547, 2005.

P. L. Yeagle, “Lipid regulation of cell membane structure and function,” The FASEB Journal, vol. 3, no. 7, pp. 1833–1842, 1989.

P. Venditti, M. Balestrieri, S. di Meo, and T. de Leo, “Effect of thyroid state on lipid peroxidation, antioxidant defences, and susceptibility to oxidative stress in rat tissues,” Journal of Endocrinology, vol. 155, no. 1, pp. 151–157, 1997.

R. Mogulkoc, A. K. Baltaci, L. Aydin, E. Oztekin, and A. Sivrikaya, “The effect of thyroxine administration on lipid peroxidation in different tissues of rats with hypothyroidism,” Acta Physiologica Hungarica, vol. 92, no. 1, pp. 39–46, 2005.

K. Asayama, K. Dobashi, H. Hayashibe, Y. Megata, and K. Kato, “Lipid peroxidation and free radical scavengers in thyroid dysfunction in the rat: a possible mechanism of injury to heart and skeletal muscle in hyperthyroidism,” Endocrinology, vol. 121, no. 6, pp. 2112–2118, 1987.

Ç. A. Íşman, B. Ç. Yeǧen, and Í. Alican, “Methimazole-induced hypothyroidism in rats ameliorates oxidative injury in exprerimental colitis,” Journal of Endocrinology, vol. 177, no. 3, pp. 471–476, 2003.

M. Rodriguez-Pierce, I. R. S. Sosenko, P. Whitney, and L. Frank, “Propylthiouracil treatment decreases the susceptibility to oxygen radical- induced lung damage in newborn rats exposed to prolonged hyperoxia,” Pediatric Research, vol. 35, no. 5, pp. 530–535, 1994.

T. Allen and S. V. S. Rana, “Oxidative stress by inorganic arsenic: modulation by thyroid hormones in rat,” Comparative Biochemistry and Physiology C: Toxicology and Pharmacology, vol. 135, no. 2, pp. 157–162, 2003.

R. Bruck, D. Frenkel, H. Shirin et al., “Hypothyroidism protects rat liver from acetaminophen hepatotoxicity,” Digestive Diseases and Sciences, vol. 44, no. 6, pp. 1228–1235, 1999.

M. J. Coria, A. I. Pastrán, and M. S. Gimenez, “Serum oxidative stress parameters of women with hypothyroidism,” Acta Biomedica de l'Ateneo Parmense, vol. 80, no. 2, pp. 135–139, 2009.

S. Yilmaz, S. Ozan, F. Benzer, and H. Canatan, “Oxidative damage and antioxidant enzyme activities in experimental hypothyroidism,” Cell Biochemistry and Function, vol. 21, no. 4, pp. 325–330, 2003.

S. Taş, M. Dirican, E. Sarandöl, and Z. Serdar, “The effect of taurine supplementation on oxidative stress in experimental hypothyroidism,” Cell Biochemistry and Function, vol. 24, no. 2, pp. 153–158, 2006.

H. Erdamar, H. Demirci, H. Yaman et al., “The effect of hypothyroidism, hyperthyroidism, and their treatment on parameters of oxidative stress and antioxidant status,” Clinical Chemistry and Laboratory Medicine, vol. 46, no. 7, pp. 1004–1010, 2008.

N. Nanda, Z. Bobby, and A. Hamide, “Oxidative stress and protein glycation in primary hypothyroidism. Male/female difference,” Clinical and Experimental Medicine, vol. 8, no. 2, pp. 101–108, 2008.

P. Pasupathi and R. Latha, “Free radical activity and antioxidant defense mechanisms in patients with hypothyroidism,” Thyroid Science, vol. 3, no. 12, pp. CLS1–CLS6, 2008.

G. Baskol, H. Atmaca, F. Tanriverdi, M. Baskol, D. Kocer, and F. Bayram, “Oxidative stress and enzymatic antioxidant status in patients with hypothyroidism before and after treatment,” Experimental and Clinical Endocrinology and Diabetes, vol. 115, no. 8, pp. 522–526, 2007.

Y. Yang, J.-Z. Cheng, S. S. Singhal et al., “Role of glutathione S-transferases in protection against lipid peroxidation: overexpression of hGSTA2-2 in K562 cells protects against hydrogen peroxide-induced apoptosis and inhibits JNK and caspase 3 activation,” The Journal of Biological Chemistry, vol. 276, no. 22, pp. 19220–19230, 2001.

T. Grune, K. Merker, G. Sandig, and K. J. A. Davies, “Selective degradation of oxidatively modified protein substrates by the proteasome,” Biochemical and Biophysical Research Communications, vol. 305, no. 3, pp. 709–718, 2003.

T. Nyström, “Role of oxidative carbonylation in protein quality control and senescence,” The EMBO Journal, vol. 24, no. 7, pp. 1311–1317, 2005.

H. Sies, “Glutathione and its role in cellular functions,” Free Radical Biology and Medicine, vol. 27, no. 9-10, pp. 916–921, 1999.

V. Fernandez and L. A. Videla, “Hepatic glutathione biosynthetic capacity in hyperthyroid rats,” Toxicological Letters, vol. 89, no. 2, pp. 85–89, 1996.

S. Torres, B. P. Díaz, J. J. Cabrera, J. C. Díaz-Chico, B. N. Díaz-Chico, and A. López-Guerra, “Thyroid hormone regulation of rat hepatocyte proliferation and polyploidization,” American Journal of Physiology: Gastrointestinal and Liver Physiology, vol. 276, no. 1, pp. G155–G163, 1999.

M. Pibiri, G. M. Ledda-Columbano, C. Cossu et al., “Cyclin D1 is an early target in hepatocyte proliferation induced by thyroid hormone (T₃),” The FASEB Journal, vol. 15, no. 6, pp. 1006–1013, 2001.

A. Alisi, I. Demori, S. Spagnuolo, E. Pierantozzi, E. Fugassa, and S. Leoni, “Thyroid status affects rat liver regeneration after partial hepatectomy by regulating cell cycle and apoptosis proteins,” Cellular Physiology and Biochemistry, vol. 15, no. 1–4, pp. 69–76, 2005.

U. Ziegler and P. Groscurth, “Morphological features of cell death,” Physiology, vol. 19, no. 3, pp. 124–128, 2004.

G. Majno and I. Joris, “Apoptosis, oncosis, and necrosis: an overview of cell death,” American Journal of Pathology, vol. 146, no. 1, pp. 3–15, 1995.

X.-W. Huang, Z.-Y. Zhao, and C. Ji, “Effects of hypothyroidism on apoptosis and the expression of Bcl-2 and Bax gene in the neonatal rat hippocampus neurons,” Chinese Journal of Pediatrics, vol. 43, no. 1, pp. 48–52, 2005.

O. A. Sukocheva and D. O. Carpenter, “Anti-apoptotic effects of 3,5,3′-tri-iodothyronine in mouse hepatocytes,” Journal of Endocrinology, vol. 191, no. 2, pp. 447–458, 2006.

Y.-F. Chen, S. Kobayashi, J. Chen et al., “Short term triiodo-l-thyronine treatment inhibits cardiac myocyte apoptosis in border area after myocardial infarction in rats,” Journal of Molecular and Cellular Cardiology, vol. 44, no. 1, pp. 180–187, 2008.

B. Bhimte, B. K. Agrawal, V. K. Sharma, and S. S. Chauhan, “Oxidative stress status in hypothyroid patients,” Biomedical Research, vol. 23, no. 2, pp. 286–288, 2012.