Potentials of curcumin against polycystic ovary syndrome: Pharmacological insights and therapeutic promises

Polycystic ovary syndrome (PCOS) is a common hormonal disorder among women (4%–20%) when the ovaries create abnormally high levels of androgens, the male sex hormones that are typically present in women in trace amounts. The primary characteristics of PCOS include oxidative stress, inflammation, hyperglycemia, hyperlipidemia, hyperandrogenism, and insulin resistance. Generally, metformin, spironolactone, eflornithine and oral contraceptives are used to treat PCOS, despite their several side effects. Therefore, finding a potential candidate for treating PCOS is necessary. Curcumin is a major active natural polyphenolic compound derived from turmeric (Curcuma longa). A substantial number of studies have shown that curcumin has anti-inflammatory, anti-oxidative stress, antibacterial, and anti-apoptotic activities. In addition, curcumin reduces hyperglycemia, hyperlipidemia, hyperandrogenism, and insulin resistance in various conditions, including PCOS. The review highlighted the therapeutic aspects of curcumin against the pathophysiology of PCOS. We also offer a hypothesis to improve the development of medicines based on curcumin against PCOS.

PCOS is a phenotype characterized by a self-reinforcing vicious cycle of neuroendocrine, metabolic, and ovarian dysfunction [6]. The pathophysiology of PCOS includes genetic and epigenetic changes, ovarian abnormalities, and neuroendocrine alterations. Primary abnormalities in the hypothalamic-pituitary axis, insulin secretion, and ovarian function are involved in the pathophysiology of PCOS [7,8]. In addition, PCOS is linked to hormonal imbalances such as hyperandrogenemia (HG), insulin resistance (IR), and hyperinsulinemia [7,9]. 60-95% of women with PCOS have insulin resistance, aggravated by increased visceral adiposity [10]. The PCOS for 12 weeks improved body weight, glycemic management, blood lipids except for triglycerides and very low-density lipoprotein (VLDL)-cholesterol levels, Peroxisome proliferated-activator receptor gamma (PPAR-γ) and low-density lipoprotein receptor (LDLR) gene expression [38]. Curcumin even reduced oxidative stress and apoptosis-related complications in patients with PCOS [39]. Recent studies reviewed the effect of curcumin on glycemic control and lipid profiles in PCOS [40][41][42]. However, in this study, we reviewed the data on the protective effects and intrinsic mechanisms of curcumin against the pathophysiology of PCOS.

Methods
This systematic review was carried out following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines ( Fig. 1) [43]. The literature was collected from published online research databases such as Scopus, PubMed, and Google Scholar using the keywords 'curcumin on PCOS' and 'curcumin on oxidative stress, inflammation, lipid state, apoptosis, hyperglycemia, and hyper androgen etc. The information was retrieved from 2016 to Jan 15, 2022. Some of the items were eliminated using automatic search tools, while others were personally reviewed. Non-English language publications of articles were not included. This evaluation did not include any reviews, book chapters, expert comments, conference papers, or letters to the editors. All figures were generated using MS Power Point.

Pharmacological effects of curcumin ON PCOS
The pharmacological potential of curcumin against some plausible factors (such as oxidative stress, inflammation, and other pathologies, as shown in Figs. 2-7 and Tables 1-2 responsible for PCOS are summarized in this section. Oxidative stress emerged as a result of these events. On the other hand, in curcumin-induced models, the expression of CAT, SOD, and GPX are activated, which then activate GSH. These stressors inhibit the expression of oxidative stress suppressive factors. ROS, and H 2 O 2, related to oxidative stress, were decreased by GSH. GSH is also capable of reducing oxidative stress.

Oxidative stress
During oxidative stress, the intracellular defense reactions are diminished, thus failing to safeguard cells against reactive oxygen species (ROS) (hydroxyl radicals, superoxide anion, hydrogen peroxide, etc.). These events eventually lead to irreparable cellular injury. ROS, the highly reactive derivatives of molecular oxygen, is formed by successive reductions of oxygen [44]. ROS synthesis and breakdown occur in the cells in a balanced manner. Disruption in this balance can accelerate the oxidative stress state in cells [45][46][47].
Different studies have reported curcumin as a potent antioxidant agent and free radical scavenger (Fig. 2). The functional groups of curcumin that contribute to the antioxidant activity are the hydroxyl (-OH) group and methylene (-CH 2 -) group of the β-diketone moiety [48]. In the estradiol-valerate induced PCOS in Wistar rats, curcumin treatment declined ROS production [36]. Additionally, in a physiological state, several antioxidants protect against the deleterious effect of oxygen-free radicals. Examples of well-known antioxidants include glutathione (GSH), water-insoluble vitamin E, water-soluble vitamin C, and some endogenous enzymes (glutathione-S-transferase, superoxide dismutase, catalase, and glutathione peroxidase) [49]. A study on letrozole-treated female Wistar rats showed a high level of oxidative markers and reduced antioxidant enzyme activity such as superoxide dismutase (SOD), GSH, and catalase. After curcumin treatment, the activity of these enzymes was increased [50,51]. Oxidative stress produces free radicles leading to lipid peroxidation by attacking the polyunsaturated fatty acid. Lipid peroxidation produces thiobarbituric acid reactive substances (TBARS) and malondialdehyde (MDA) as by-products. Hence, TBARS and MDA are oxidative stress markers [52,53]. According to a Fig. 3. Anti-inflammatory effect of curcumin. The stress stimuli increased NF-кB binding activity. NF-кB in cytosols goes to the nucleus, binds to DNA, and activates TNF-alpha, IFN-γ, IL1, IL-6, IL-10 and COX-2. iNOS is also expressed, which next activates NO. These markers are associated with inflammation. On the other hand, in the curcumin-induced model, Nrf2, IL-SIRT1, and PGC-1 alpha are activated, downregulating the inflammation state. They also downregulate the expression of NF-кB. study, TBARS synthesis increased in female model rats with PCOS. The level reached normal with curcumin treatment [50]. Sodium arsenite-induced oxidative stress caused gradual elevation in oxidative stress markers in Kunming mice [54]. Subsequent curcumin treatment reduced ROS synthesis. However, the antioxidant enzyme SOD and Gpx increased in curcumin-treated mice [54]. Besides, an increased MDA level was demonstrated in sodium arsenite and letrozole-induced model animal studies, respectively. But curcumin minimized the MDA level in both cases [51,54].
A clinical trial conducted on female patients with PCOS reported higher Gpx and SOD activity, followed by curcumin therapy [40,55].

Inflammation
Chronic inflammation contributes to the etiology of PCOS. The inflammatory process is caused by the augmentation of several inflammatory elements, such as pro-inflammatory cytokines and chemokines [56][57][58]. TNF-α is an inflammatory cytokine that is crucial for both ovulation and pregnancy. This cytokine is commonly found in theca cells, macrophages, granulosa cells and oocytes. It triggers the proliferation of follicular theca cells. But, excessive expression of TNF-α in adipose tissue may result in high blood glucose levels and insulin resistance [59]. It can influence the insulin signaling pathway and develop insulin resistance [60,61]. TNF-α causes insulin resistance by stimulating serine phosphorylation of insulin receptor substrate-1(IRS-1) and interfering with the functions of β cells [62][63][64]. Another cytokine IL-6 regulates inflammation and governs the production of different cytokines [65]. It is essential in ovarian maturation and implantation procedure [59]. The elevated amount of TNF-α followed by excessive production of IL-6 monocytes is found in the serum of women with PCOS, causing low-grade inflammation [66,67].
Curcumin can interact with these cytokines as a potent anti-inflammatory agent (Fig. 3) [68]. It serves as a PI3K/AKT/mTOR Fig. 4. Effect of curcumin against hyperglycemia. Stress stimuli increase insulin resistance via triggering the glucose, HBA1c, FIS, FBG, and HOMA-IR and downregulate insulin production. The Hyper-glycaemia stage is created. On the other hand, insulin production is increased in curcumininduced models, and the hyperglycemia stage is downregulated.
signaling pathway inhibitor and, therefore, downregulates the expression of TNF-α along with several pro-inflammatory cytokines [69,70]. The nano-curcumin treatment decreased the serum TNF-α levels in letrozole-induced rat models [51]. Likewise, orally administered curcumin in DHEA-induced Sprague-Dawley female rats significantly reduced pro-inflammatory cytokine production [71]. In another study, curcumin treatment reduced serum levels of CRP, TNF-, and IL-6 in PCOS-induced Wistar rats [72]. Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB) is a ubiquitous and pro-inflammatory transcription factor. It regulates immune response by triggering the synthesis and releasing various cytokines or inflammatory factors, such as TNF-α, IL-6, IL-10, IL-18, TGF-β, and IFN-γ [73]. The amount of NF-кB, TNF-α, COX-2, iNOS kinase and IFN-γ was declined in the PCOS-induced Wistar rat after curcumin treatment. The activation of NF-κB is suppressed by curcumin in different cell lines. This inhibitory effect is produced by restricted I kappa B kinase (IKK) activity and is prompted by TNF, IL-1, hydrogen peroxide (H 2 O 2 ), and phorbol ester. Hence, the diminution of NF-кB reduces the activity of certain inflammatory enzymes like iNOS kinase and COX-2 [36]. The activity of peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) is interconnected with inflammation. During the inflammatory state, the activity of PGC-1α is repressed. This event accelerates the inflammatory response [74,75]. Nuclear Factor Erythroid-2 (Nrf2) is a transcriptional factor that inhibits inflammation. It impedes the expression of pro-inflammatory cytokine genes (IL-6 and IL-1b) [76]. SIRT1 inhibits the role of NF-кB complex as a transcription factor as it deacetylates the RelA/p65 (lysin-310 residue) [77]. The overexpression of SIRT1 reduced IL-6 and TNF-α by downregulating NF-кB activity in the liver [78]. Curcumin therapy increased the level of SIRT-1, Nrf-2, and PGC-1α in an experiment conducted on patients with PCOS. Also, nanocurcumin dramatically increased the expression of miR-223-3p and decreased NF-kB to replenish ß cell mass in the pancreas of rat model of PCOS [79].
Another outcome of a clinical trial depicted that circulating TNF-α, IL-6 and other pro-inflammatory cytokine levels diminished in women with PCOS after curcumin therapy [40]. CRP, produced by the human hepatocyte, is considered an indicator or marker of the inflammatory process and is positively regulated by TNFα and IL-6 [80]. This acute-phase reactant acts as an inflammation mediator by inducing endothelial dysfunction and promoting MCP-1-mediated chemotaxis [81]. Moreover, an elevated amount of high sensitivity CRP is a significant prognosticator of cardiovascular disease and is closely associated with insulin resistance [82,83]. After curcumin supplementation therapy, women with PCOS demonstrated decreased CRP expression in two separate studies [37,84].

Hyperglycemia
PCOS is a metabolic disease linked with type 2 diabetes mellitus (DM2) that begins with hyperglycemia and progressively leads to insulin resistance [50,85]. Insulin resistance affects up to 70% of women with PCOS [61]. Women with PCOS develop impaired glucose metabolism at an earlier age and may progress more quickly from impaired glucose tolerance (IGT) to DM2 [86]. Insulin resistance is often accompanied by an increase in endogenous insulin synthesis as a compensatory mechanism. Insulin resistance is linked to high amounts of endogenous insulin, which leads to weight gain, eventually exacerbating insulin resistance [87,88]. This vicious cycle continues until pancreatic beta-cell activity can no longer match the increased insulin demand caused by insulin resistance, resulting in hyperglycemia. Glycemic levels rise to levels compatible with DM2 when the mismatch between insulin demand and production persists, called hyperglycemia. Curcumin has increased insulin sensitivity substantially and reduced insulin resistance (Fig. 4) [89]. In addition, glucose tolerance is promoted by curcumin treatment in certain experimental models [90]. According to direct experimental data, curcumin increases glucose tolerance by stimulating glucagon-like peptide-1 (GLP-1) production [91]. Curcumin has anti-inflammatory and antioxidant properties, which are vital in improving beta-cell functions [92]. Beta cell secretes insulin which assists glucose uptake by the liver or muscle from blood [93]. Therefore, blood glucose level remains balanced.
Moreover, curcumin shows antidiabetic effects in the liver by increasing glycolysis and glycogen synthesis while decreasing gluconeogenesis and in the skeletal muscle by increasing glucose absorption, glycolysis, and glycogen synthesis [94]. Curcumin can lower blood glucose levels by reducing endogenous glucose production, suppressing hyperglycemia-induced inflammation, and stimulating glucose uptake. Additionally, curcumin reduces blood glucose by upregulating the expression of the glucose transporter Fig. 6. Effect of curcumin against hyperandrogenism. LH, estradiol stimulated by stress stimuli. These hormones stimulate-+ androgen testosterone and DHEA, which leads to the hyperandrogenism stage involved in inducing PCOS. In contrast, the curcumin-induced model stimulates progesterone and FSH hormone production. Progesterone lowers the androgen level. FSH increases the binding activity of androgen. Progesterone, FSH together helps to minimize the hyperandrogenism stage. type 4 (GLUT4), GLUT2, and GLUT3 genes, activating AMP kinase, promoting peroxisome proliferator-activated receptor (PPAR) ligand-binding activity, stimulating insulin secretion from pancreatic tissues, improving pancreatic cell function, and lowering insulin resistance [95]. The glycemic profile of the curcumin-treated experimental model is reported in Table 1. Mice administered with DHEA were treated with 5.4 mg/100 g for twenty consecutive days showed decreased insulin levels [96]. Curcumin treatment reduced fasting blood glucose (FBG), fasting insulin (FINS), and homeostatic model assessment of insulin resistance (HOMA-IR) in DHEA-treated Sprague-Dawley female rats [71]. Female Albino Wistar rats were treated with curcumin for 15 days and decreased letrozole-induced glucose and hb1c level [50,51]. In another study, curcumin treatment reduced blood glucose levels and insulin in estradiol-valerate injected Wistar rats [36]. Nanocurcumin also attenuated the insulin resistance in letrozole-induced Wistar rats [79]. A group of PCOS-affected women, varying from 18 to 40 years old, were treated with curcumin for 12 weeks, which decreased fasting plasma glucose (FPG), HOMA-IR and increased QUICKI [38]. Women with PCOS aged 18 to 49 were treated with curcumin for 12 weeks and manifested a low level of FPG, FBS and insulin [39]. In another clinical trial of 60 women with PCOS, curcumin treatment reduced HOMA-IR, FBS and HbA1c [37].

Hyperlipidemia
Women suffering from PCOS may possess lipid abnormalities. According to a recent study, women with PCOS typically have Fig. 7. Anti-apoptotic effect of curcumin. Stress stimuli induced BAX and CASP3 production. BAX can transmit cell death via apoptosis through the mitochondrial external membrane. Caspase-3 coordinates cellular structure breakdown, like DNA fragmentation or cytoskeletal protein degradation. In contrast, curcumin stimulated Bcl2 which prevents BAX/BAK oligomerization, thus preventing apoptosis. moderate hypercholesterolemia [97]. PCOS has different lipid patterns, including low levels of high-density lipoprotein cholesterol (HDL-C), high triglyceride (TG), total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C), as well as considerably greater lipoprotein concentrations [98,99]. The C677T polymorphism of the methylenetetrahydrofolate reductase (MTHFR) gene reduces MTHFR enzyme activity, leading to hyperhomocysteinemia, which is linked to hyperlipidemia [100].
Curcumin exerts cholesterol-lowering effects on humans and animals. It inhibits the accretion of blood cholesterol concentrations in animal experiments by reducing dietary cholesterol absorption (Fig. 5) [101]. Curcumin mainly lowers blood and hepatic cholesterol levels by blocking the 3-hydroxy-3-methyl-glutaryl-coenzyme a reductase (HMG-CoA reductase) enzyme [102]. Curcumin has been shown to promote CYP7A1 enzymatic activity by raising its hepatic gene expression, resulting in increased cholesterol clearance as bile acids [103]. Curcumin suppressed glycerol release while improving glucose absorption by activating PPARγ and CCAT/enhancer-binding protein-α (CEBPA) [104]. A recent study reported that curcumin inhibited the production of ldlr (the gene that encodes for the protein known as the low-density lipoprotein receptor) and decreased the absorption of extracellular LDL via inhibiting sterol regulatory element-binding protein-2 (SREBP-2) gene expression and activity [105]. The lipid profile of the curcumin-treated experimental model is presented in Table 1. Letrozole-injected female Wister rats were treated with curcumin which decreased TC, TG, LDL and raised the level of HDL [50]. Raoofi et al. demonstrated that triglyceride, cholesterol, LDL, HDL and VLDL were significantly increased in curcumin-treated female Wistar rats [106]. Various studies among PCOS-affected women showed that curcumin lowered TG, LDL and cholesterol in the blood and increased HDL and VHDL [37][38][39]51]. Different bioactive components of curcumin have been linked to anti-lipid and other metabolic benefits in animal studies. Tetrahydrocurcumin, ferulic acid and vanillic acid are examples of these, all of which are curcumin metabolites. Curminoids (diarylheptanoid, demethoxycurcumin, and curcuminoids), bisdemethoxycurcumin, desmethoxycurcumin, and methoxycurcumin are different types of curcumin [107,108]. However, the effects of curcumin on HDL, LDL, and triglycerides are still being studied, and further research is needed to confirm these findings [40].

Hyperandrogenism
Hyperandrogenism refers to a condition in which the number of androgens (male hormones) in females exceeds the normal range. Ovarian and extra-ovarian hyperandrogenism are prominent symptoms of PCOS [109]. PCOS is the most prevalent endocrine condition in women of reproductive age, with a frequency ranging from 5% to 15% [110,111]. The hyperandrogenic state in the ovary is caused by androgen production in the ovarian theca cells [109]. Increased ovarian androgen levels are a common sign of hyperandrogenism in PCOS, resulting in poor follicular maturation. Elevated androgens levels may deleteriously influence follicular growth, resulting in atresia. Generally, the ovaries are the primary source of androgen abundance in PCOS patients. However, 20-30% of PCOS individuals have elevated adrenal androgen levels [112,113].
The majority of available PCOS drugs are androgen inhibitors. Several derivatives of curcumin suppress androgen action (Fig. 6). In letrozole-injected female Wistar rats, curcumin inhibited LH and stimulated FSH [114]. In another experimental model of estradiol valerate injected Wister rats, curcumin downregulated LH, testosterone, and estradiol production and upregulated FSH synthesis [106].
Clinical trials of curcumin extract or compounds on women with PCOS exhibited outcomes analogous to animal experiments. In a clinical trial on women with PCOS, curcumin extract or compounds inhibited insulin and dehydroepiandrosterone (DHEA) [40]. Another trial showed that women (18-49 years old) with PCOS for at least two years, curcumin (1500 mg/day for 12 weeks) suppressed DHEA and stimulated estradiol instead of repression [39]. Thirty newly diagnosed women with PCOS were given a daily dose of 93.34 mg (2 capsules) for eight weeks, demonstrating similar inhibition activity by reducing testosterone, LH, FSH, and DHEA [84]. Women with PCOS 500 mg-1500 mg per day for 6-12 weeks -Improve glycemic control and lipid metabolism -Alleviated metabolic abnormality ↓NF-κB, ↓TNF-α, ↓IL-6, ↓DHEA,↑GPx, and ↓insulin, [40] Women (18-49 years)

Other pathological effects related to PCOS
According to clinical research, apoptosis is seldom identified in the glandular epithelium during the proliferative phase or at the starting point of the secretory phase of the menstrual cycle [115]. Despite the absence of quantification, the number of apoptotic bodies in epithelial cells in PCOS patients without hyperplasia is higher than in non-PCOS controls and PCOS patients with hyperplasia [116].
In line with this, the following curcumin extracts or isolated compounds have been reported to protect PCOS (Fig. 7). Curcumin compounds have been shown to prevent apoptosis in several investigations. In a study of DHEA administered prepubertal BALB/c mice, curcumin inhibited the activity of BCL2-associated X (BAX), Caspase 3 (CASP3), and insulin but enhanced B-cell lymphoma 2 (Bcl2) expressions [117]. Excess androgen can cause cell death via various signaling mechanisms through Klotho expression [118]. Hyperandrogenism in PCOS may potentially induce apoptosis in oocytes. Heat shock protein 27 (HSP27), an anti-apoptotic protein in the HSP family, is dramatically downregulated in PCOS oocytes [119]. Nanocurcumin also showed to restore the ß cell mass by erupting autophagy [79].

Future prospects and limitations
Women with PCOS are susceptible to several metabolic disorders, and the current studies have demonstrated the effectiveness of curcumin against PCOS [120]. Studies on rat models and female patients with PCOS pointed out that curcumin treatment positively influences the PCOS-associated parameters (Fig. 8) [50]. Curcumin treatment reduces the oxidative markers, including ROS, TBARS and MDA, in rat models. It also alters the gene expression of SIRT1 and PGC-1α [36,52,53,55]. In experimental PCOS models, curcumin has enhanced the functionality of different antioxidant enzymes, such as SOD, GSH, catalase and GPX [40,50,51,55]. Curcumin lowers blood glucose, so it can be used in treating diabetes [95]. One study showed that curcumin works synergistically with metformin to improve insulin resistance and lipid profile in PCOS patients. As a result, the combination of metformin and curcumin may have Fig. 8. Protective potentials of curcumin against polycystic ovarian syndrome. Letrozole, Estradiol-valerate, DHEA causes PCOS in different pathways (oxidative stress, inflammation, hyperglycemia, hyperlipidemia androgen stress, apoptosis) and those pathways can be inhibited by curcumin. In various research models such as rats, and mice, these stress stimuli increase insulin resistance through increasing insulin resistance factors (HBA1c, glucose, FIS, FBG) which results in hyperglycemia. These stress stimuli also increase LDL, VLDL, TG, etc., which results in hyperlipidemia. The increased rate of NF-ҡB also induce iNOS, NO, COX-2, ILs. These factors indicated inflammation in PCOS. Oxidative stress is another pathway activated via increased ROS production, MDA, etc. Male hormones were increased in response to those stress stimuli, resulting in hyperandrogenism. Another pathway, apoptosis, is stimulated via the increased production of CASP3 and BAX. Curcumin has inhibitory activity against these pathways. Curcumin can regulate the production of insulin resistance factors. It increases the production of HDL, which decreases the condition of hyperlipidemia. Curcumin also increases the anti-inflammatory factors. Curcumin inhibited oxidative stress by upregulating SOD, GPX, GSH, and Catalase. Curcumin can also stimulate the expression of FSH and progesterone, which can control the hyperandrogenism state. Additionally, it increased the expression of the Bcl2 gene, which is an anti-apoptosis factor. Therefore, curcumin can improve the condition of PCOS by regulating the various pathways. therapeutic value in PCOS patients [125]. A study reviewed that curcumin helps with the treatment of metabolic syndrome, arthritis, anxiety, as well as oxidative and inflammatory diseases [121]. Clinical studies suggest that curcumin use is also quite safe when done continuously for up to 4 months [122,123].
According to previous studies, curcumin did not show any notable adverse effects; instead, it limited the serum cholesterol level [101]. However, some studies did not show any significant effect of curcumin on model rats and female patients [50]. This inadvertent result may due to the low absorption of curcumin [84]. Due to its hydrophobic nature, curcumin has poor absorption and very low solubility in water (0.005%) [84]. Its oral absorption is limited, although its usage with piperine (found in black pepper) enhances its absorption [126]. However, nanocurcumin is more efficient in reducing serum cholesterol due to its anti-hyperlipidemic potential [96,124]. Nanocurcumin treatment successfully protected pancreatic tissue from oxidative stress caused by PCOS [51]. Along with anti-cancer potentials, nano-curcumin can be one of the best medications for PCOS treatment. Nanoparticles and lipid/liposome formulations that improve curcumin absorption and bioavailability are being explored as better ways to administer curcumin [127,128]. Recent studies suggest that sonicating curcumin with chitosan, N-acetyl histidine, and arginine is a gateway into nanomedicine. It has been more stabilized in watery media than free curcumin. Therefore, this characteristic is attributed to an improved drug delivery system of curcumin-loaded nanoparticles. FSH, LH, and testosterone reached their normal level compared to free curcumin drug-treated or metformin-treated mice models [129].
Considering, the advancement and refining of these technologies will allow for cell-directed curcumin targeting and better treatment outcomes against PCOS.

Conclusions
PCOS is associated to oxidative stress, inflammation, insulin resistance, and hyperandrogenism, making individuals vulnerable to diabetes, endometrial cancer, and cardiovascular disease [130,131]. The current review illustrates various therapeutic properties of curcumin including anti-diabetic, antioxidant, anti-inflammatory, and anti-androgenic effects (Fig. 8). It plays a remarkable role in alleviating the lipid metabolism and glycemic profile in patients with PCOS and model rats. In addition, curcumin is affordable and readily available [132]. These diversified characteristics of curcumin can enlist it as a promising therapeutic herbal medicine in treating PCOS. However, curcumin has low solubility and poor body pH bioavailability. So, the limitation can be considered an impediment to its widespread use [133]. Bio-compatible nanocurcumin has an increased polarity compared to the natural one [51]. In order to reduce autophagy flare, insulin resistance, and boost ß cell mass, nanocurcumin markedly increased the expression of miR-223-3p in the pancreas of rat model of PCOS [79]. Hence, the formulation of nanocurcumin and additional research for its optimization and application as a therapeutic agent may overcome the hurdle of solubility and bioavailability.