Medires Publishers - Article

Abstract

Food preservatives are chemical or natural substances that are added to the food products which will help to increase the shelf life and also inhibits the growth of microorganisms that causes food spoilage. The objective of review is to know and understand the adverse effects of chemical preservative in food products. Even though the chemical preservative used is approved by the FDA, whereas the long-term usage of some preservatives can causedifferent health problems in humans including cancer. This review is also intended to understand how the preservative induce different health problem in the body if consumed for long term. It is not possible to review all the preservatives hence, mainly focused on sodium sulphite, sodium nitrite, sodium benzoate, Tertiary butylhydroquinoe (tBHQ) and Butylated hydroxylanisole (BHA) which are commonly used food preservatives in beverages, dried foodproducts, meat and other processed food. The long-term consumption of the food which is treated with the above-mentioned food preservatives showed signs of carcinogenicity, genotoxicity and other allergies. In future the usage of natural food preservative which is derived from plants and other natural sources can make a drastic change in growing health problems using chemical preservatives. 

Introduction

Preservatives are chemical or natural compoundsthat helps to inhibit the growth of microorganisms whichresults in food spoilage by inhibiting or stopping the fermentation, acidification or other decomposition of food. They also help to increase the shelf life of the food by preventing it from spoilage. Due to the increase in ready to eat and convenient foods has increased, the demand for chemical preservatives in market also came to a sudden rise (Mirza et al., 2017). Among the preservatives which are widely being used today, sodium chloride (salt) is perhaps the oldest preservative.

The use of food additives is directed by particular laws (specifically within the European Union - EU), considering the food where it can be used, most in usable amounts, chemical characterization and purity (Silva and Lidon, 2016). Long-term rat experiments revealed that large amounts of nordihydroguaiaretic acid (antioxidant) in diet were transformed to the corresponding orthoquinone, which is likely the source of the fecal bleeding and ulceration, as well as the mesenteric cysts. The alkyl gallates (antioxidants) in oils, margarine, sausage and meats were discovered to cause dermatitis in bakers and others who worked with alkyl gallates leads to cheek sensitization in a few customers; it was determined that a major cause of cheek sensitization was the consumption of large amounts of beer and other beverages treated with alkyl gallates, so the use of alkyl gallates as antioxidants in beer and other beverages was discontinued. (Parke and Lewis, 1992).

Several writers have examined the mutagenic and/or genotoxic effects of potassium sorbate, which is used as an antibacterial agent in a broad range of foods such as cheeses, pickles, sauces, soft beverages, and other goods with the SCEs test, potassium sorbate seemed to have a modest genotoxic impact at two (4 and 8 mM) of the five (0.02, 0.2, 2, 4, and 8 mM) concentrations tested in human lymphocytes. Other results obtained in Chinese Hamster cells at 3-4 mg/ml concentration with Chromosomal aberration test and in Chinese Hamster V79 cells at 20 mg/ml concentration with CAs, SCEs, and gene mutation assays support a modest genotoxic impact. (Mamur et al., 2010).

It is not possible to review all the preservatives that causes the adverse effect, hence the chemical preservatives that are discussed in this article are:

• Sodium sulphite
• Sodium nitrite
• Sodium benzoate
• Tertiary butylhydroqunione (tBHQ)
• Butylatedhydroxyanisole (BHA)

Sodium sulphite

Sulphite is a popular food preservative that is widely used as a blanchingagent and preservative in a varietyof food products to enhance the appearance of the food product. They're also utilised to prevent food from oxidizing and can be employed to give a product a fresh scent and flavor.In general, they are regardedsafe substances, but only when used in the smallest amount possible, Sodium sulphite, potassium bisulphite, and sodium bisulphite are only a few examples (El-Hefny et al., 2021). 

Several allergic responses have been recorded in persons who have been exposed to sulphite- containing foods. Sulphite is a potentially deadly chemical that can be ingested, inhaled, or infused into the body. Rats administered with precise doses of sodium sulphite twice a week, the results revealed severe impacts on both liver and kidney cells. Sulphite compounds have been shown to have detrimental and hazardous effects on people. (Mahmoud et al., 2015).

Mechanism of action

When sulphite is in contact with stomach acids SO2 is formed this production on SO2 will get enhanced when the temperature is high and the pH is low. The acidic and warm conditions in the stomachand mouth are efficient for the production of SO2. Which causes asthma in some people. Sulphite also induces a health condition known as bronchospasm in individuals who are sensitive to sulphite, deathsare also reporteddue to sulphite sensitivity (Lester,1995). Sulphite sensitivity is commonly seen in patients with asthmatic condition, but sulphite-induced health problems may be seen inpatients without recorded asthma or other allergy-related disorders (Rangan and Barceloux, 2009).

Adverse effect Sulphite sensitivity

According to the Food and Drug Administration (FDA), one out of every hundred personsis sulphite-sensitive, and 5   % of that group has asthma. According to another source, 5% of asthmatics are sulphite sensitive, compared to only 1% of the general population. Sulphite intolerance symptoms might appear as soon as 5 minutes after parenteral exposure and 15-30 minutes after oral consumption. Individuals with sensitivity to sulphites have varying degrees of intolerance, with each having a different threshold for eliciting a response. In experimental animals, sulfiting agents are neither, teratogenic, mutagenic, or carcinogenic; nonetheless, a small percentage of the population is sulphite sensitive and vulnerable to a variety of side effects owing to acute allergic responses. Many allergic reactions have occurred in some people after consuming sulphite-containing food products, including urticaria, angioedema, hives and pruritus, flushing, tingling, and swelling; respiratory symptoms such as dyspnea, wheezing, and 

bronchoconstriction; and gastrointestinal symptoms such as nausea and stomach cramps. (Grotheer, Marshall and Simonne,2005).

Sodium nitrite

Sodium nitrite is a preservative mainly used to preservemeat products. They give bright red colourto meat products like beef and sausages. Nitrite is an active compound of nitric oxide which is formed when nitrite is dissolved. During the process of preservation of meat, the nitric oxide reacts with the meat pigment known as myoglobin to give its bright red colour this combination will produce a compound known as nitrosomioglobinwhich is considered as a carcinogenic compound (Ambarwati, 2012).

The long-term consumption of processed meat that contain nitrites has shown the development of colorectal cancer (Crowe et al., 2019). Long term exposureto N-nitroso-compounds can cause esophageal carcinoma.  Nitrites are also involved in the synthesis of N-nitroso-compounds (Xie et al., 2011). Sodium nitrites can induce colonic aberrant crypts. Colonic aberrant crypts are putative preneoplastic lesions for colon cancer. Experiments using rats were done to study the effects of sodium nitrite (Zhou et al., 2016). 

The results showed that the rats which was treated with sodium nitrite showed a small decrease in serum cholinesterase activity after 3-6 months of treatment (Helal et al., 2008). When nitrates are consumed, they are converted to nitrites, which can combine with haemoglobin to form methemoglobin, which can cause loss of consciousness and death, especially in newborns (Anand and Sati, 2013).It's possible that sodium nitritetherapy caused foetalmethemoglobinemia, which led to an increased requirement for new red blood cells (Globus and Samuel, 1978).

Mechanism of action

Among the various chemical carcinogens that have been recognized in human food and drink, N-nitrosocompounds are exceptionally strong. N-nitroso compounds are generally formed by the combination of a secondary amino compound with a nitrite (Lijinsky, 1999).Nitrite is an active compoundof nitric oxide which is formed when nitrite is dissolved. During the process of preservation of meat, the nitric oxide will get combined with the meat pigmentknown as myoglobin to give its bright red color this compound is known as nitrosomioglobin which is considered as a carcinogenic compound (Ambarwati, 2012). 

Adverse effect

Formation of n-nitroso-compounds

Traces of NDMA were also found in cooked bacon. Nitrosomine and nitrosothiazolidine were discovered in bacon and other cured pork products and were generated by the interaction of cysteine, formaldehyde, and nitrite. There are reports showing the presence of nitrosodi-n-butaylamine in some meat products but at a very low concentration. This nitrosamine is a main compound for inducing tumours in the urinary bladder of rats (Kadhum et al., 2015). In many Asian countries there were persistent reporting of nasopharyngeal cancer. On testing the samples of fish traces of NDMA was found. NDMA is an inducer for liver, kidney and lung tumours (Lijinsky, 1999). In fried bacon the presence of two volatilen-nitrosamines is alwaysdetected they are N-nitroso-sodimethlylamine and N- nitrosopyrrolidine (Joseph, 1988).

Santarelli et al., 2010 conducted two studies on female rats, one for fourteen days and the other for one hundred days. In the fourteen days study the diet given to the female rats were processed pork of four   different verities (a) was dark meat crossed with (b) light meat the cooking temperature for light meat was 70o C and it wascrossed with 500C raw meat, for (c) it was the meat treated with nitrite and (d) was oxidized meat.

The nitrite treated meat was cured with salt containing 0.6g of sodium nitrite per 100 gram of salt and the non- nitrite treatedmeat was curedwith common salt. On the one hundreddays experiment they used fifty rats and they werefed with experimental diets. This was done to show the dietary promotion of cancer. The body weight of the rats was monitored every week. The faecal water from the rats were collected and was analyzed the heme concentration of the faecal water was measured. 

The processed meat that contained heme and nitritewhich was cookedfor 700c showed increased numberof preneoplastic lesionsin the rats which shows that nitrite processed meat can promote carcinogenesis (Gbemisola et al., 2020).

Sodium benzoate

Sodium benzoate is a sodium salt which is used as a preservative mainly in juices and beverages to inhibit the growth of harmful bacteria, yeast and molds. There are reports that states that, over intake of sodium benzoate treated food can cause utricaria, hyperactivity in children and also it is harmful to the DNA. Sodium benzoate is also considered to be genotoxic, neurotoxic and also it is responsible for the intercalation in DNA structure(Bruna et al., 2018).

It is also found that the long-term use of sodium benzoate treated food products might produce carcinogenic compounds when they get combined with vitamin C or ascorbic acid (Samal et al., 2017). Sodium benzoate treated food products was tested for genotoxic effects by using chromosomal aberrations, sister- chromatid exchanges and micronucleus analysis in cultured human peripheral lymphocytes and comet assay in lymphocytes (Zengin et al., 2011).

Mechanism of action

The effect of sodium benzoate on human cell lymphocytes was examined at doses of 200 and 500 g/mL. At 500 g/mL, benzoic acid increased the indices of sister chromosomal exchanges (SCEs), chromosomal aberration (CA), and Micronucleus (MN) while decreasing the mitotic division index (Mitotic index). The researchers looked at lymph node cells from mice that had been given different dosages of sodium benzoate to see if it may change the morphology of the lymphocytes and harm the cell membrane. When this chemical is exposed to higher concentrations and for longer periods of time, the negativeeffects become more pronounced (Shahmohammadi et al., 2016).

Adverse effect

Genotoxicity effectsof sodium benzoate:

To understand the genotoxicity effect of sodium benzoate preservative they used three assays chromosomal aberration, sister chromatid exchanges and micronucleus assay and it was carried out in human lymphocytes. Hungerford's standard technique was used to grow lymphocytes. Sodium benzoate showed an increased number in CA and CAs/cell in every concentration when it was comparedwith the control.

The preservative showed many structural aberrations in chromosomes like chromatid gaps, chromosome gaps, chromatid breaks, chromosomal breaks, acentric fragments and dicentric chromosomes. In the genotoxicity test they were able to detect substances that caused geneticdamage and also carcinogenic compounds. The frequency of sisterchromatid exchanges per cell is increased by sodium benzoate. In all concentrations of sodium benzoate, this rise is considerable. The increase in sister chromatid exchanges is proportional to the concentration. When the concentration of sodium benzoate is increased, the value of the cell cycle proliferation index decreasesconsiderably (Mpountoukas et al., 2008).

Table: 

Tertiary butylhydroquinone (tBHQ)

Tertiary butylhydroquinoe is food preservative used mainly in oils and some meat products. It helps to prevent rancidity and extends the shelf life of the food product, it also act as an antioxidant and prevents discoloration of    thefoods containing iron. Due to the high anti-lipid peroxidation property of tBHQ it is being widely used in fats and oils. In excessive consumption of foods containing tBHQ there is a possibility of stomach tumors and brain damage. Some studies have shown that tBHQ will cause in the formation of 8-hydroxydeoxy guanosine in calf thymus DNA due to the formation of reactive oxygen species like hydrogen peroxide and superoxide anion. It is reported that tBHQ showed cytotoxic effects on human umbilicalvein endothelial cell (huvec) in a time dependent manner. Recent studies shows that over exposure to tBHQ can cause carcinogenicity (Eskandani et al., 2014). A number of studies have shown that the excessive use of tBHQ can leadto stomach tumors and candamge the DNA (Dolatabadi and Kashanian, 2010).

Mechanism of action

The observed carcinogenic effects of tBHQ have been related to the metabolic synthesis of oxidized forms of tBHQ, their semiquinone anion radicals, and ROS formation(Gharavi et al., 2006). tBH can also induce cytoxicity It depicts the development of DNA fragmentation and breaking (Eskandani, Hamishehkar and Ezzati Nazhad Dolatabadi, 2014).

Adverse effect carcinogenicity

Studies show that tertiary butylhydroquinoe can intensify the carcinogenic effects of other chemicals when they were tested in different animalslike rats and hamsters. When rats were fed with 2% of tBHQ for about 4-8 weeks, there was an increased hyperplasia of forestomach basal cell. When the rats were fed with 2% of tBHQ without the presence of NaNO2 for about 4 weeks showed a small increase in the thickness of the forestomach mucosa. When 0.7% of tBHQ, 0.7% BHA, and 0.3% butylated hudroxytolune showed a combined effect of bladder tumours. In contrast to tBHQ alone, co-administration of 0.5–2 percent tBHQ with 0.2–0.3 percent NaNO2 for 4 or 36 weeks resulted in a more than 10-fold increase in fore stomach thickness mucosa (Saibu et al., 2020). 

Thus, it is seen that tBHQ can cause an enhancing effect in bladder cancer which is induced by N-butyl-N-(4-hybroxybutyl) nitrosamine BBN. The metabolicproduction of oxidized formsof tBHQ, their semiquinone anion radicals, and ROS generation   has been linked to the reported carcinogenic effects of tBHQ, at least in part. (Gharavi et al., 2006). F344/N rat and B6C3F mice were fed with food cured with tBHQ for about 13 weeks. Oral consumption was selected becauseof the nature of human consumption. Genetic toxicology studies were conducted in Salmonella typhimurium and cultured rat ovary cells in vitro and in vivo bone marrow cells of mouse was tested.   As a result, Introduction of tBHQ to rats in their feed resulted in diminished rates of mammary gland neoplasms in males and females (Naidenkoet al., 2021).

Cytotoxicity and DNA damage properties of tBHQ

A549 lung carcinoma cell line and HUVEC were used for the experiment. The cytoxicoty of tBHQ was determined by MTT assay. The DNA fragmentation assay was also done to identify the presence of fragmented DNA. The results for the cytotoxicity on tBHQ- treated A549 and HUVEC cells showed that tBHQ was able to induce cytotoxicity in both the cells depending upon the amountof dosage and theconsumption rate (Mirza et al., 2017).

The study also showed that the excessive intake of food treated with tBHQ can also inducecarcinogenicity. DNA fragmentation assay showed the formation of DNA-ladder which shows the formation of DNA breakage and fragmentation (Eskandani et al., 2014). Rats were given various antioxidants including tBHQ in diet to identify if the food additive inducedurinary bladder cancer.tBHQ showed weak promotion of urinary bladdercancer. They were given 0.5 % for 32 weeks as a result the rats that was fed by tBHQ diets showed increased DNA synthesis in the urinary bladderepithelium of the rats (Ito and Fukushima, 1989).

Butylated Hydroxyanisole (BHA)

Butylated hydroxylanisole is food preservative mainly used in oils and fats. It is a phenolic antioxidant. They prevent rancidity in oils and fats in food by preventing the lipid oxidation, BHA is also used in dry foods and cereals. They also maintain the freshness, colour, nutritive value of food. Many studies on BHA have shown that it promotesor induces cancer in many animals.The possibility of causing healthproblems is due to the excessive consumption of the products that contain the particular preservative. Studies have shown that BHA can cause cancer of the non-glandular stomach or the fore-stomach of male rats, in this particular study it was shown that the tumors were induced at 20000 ppm BHA in the given diet. Many other studies have shown that by 5000ppm of BHA in diet administrated to rats for about 51 week resultedin neoplasia and the increasein the squamous cell in rats (Whysner et al., 1994).

The amount administrated by FDA for the usage of BHA in beverage and desserts made from dry mixtures is between 2 ppm and for active dry yeast it is between 1000 ppm. The daily consumption of the compound that contain BHA can get close to the ADI level. Pharmaceuticals also contain BHA, if one is to consume both the diet and the pharmaceutical product on a daily basis then can result in exceeding the ADI levels (Anca et al., 2013). On A549 lung cancer cell the cytotoxic effect or the genotoxic effect of BHA and its mechanism still remainsunidentified. By MTT assay, it helped to identify that BHA can induce ctytoxicity in A549 lung cells but it depended up on the time-duration and the dosage (Vandghanooni et al., 2013).

Mechanism of action

The addition of the antioxidant BHA to the diet of F344 rats caused a significant incidence of papilloma and squamous cell carcinoma of the fore stomach in both sexes,male hamsters administered BHA developed papilloma, which grew downward into the fore stomach sub mucosa, according to carcinogenicity studiesdone by (Ito et al., 1985).

Adverse effect carcinogenicity

For this experiment five-four-week-old rats from both sexes were used as test animals. The addition of BHA to the diet of the rats were according to different levels that is from 0.5 to 2.0%. The rats of both sexes were divided into two different groupsand was given high and low amountof BHA containing diets for about 104 weeks. After that they stopped giving them the test diet and started providing them with normal diet for about 112 weeks. The rats that survived the end of 112th week were sacrificed and examined. The rats that died during the experiment were   also examined, and also that survived 41 weeks.

The first tumor appearance was in the pituitary of a female rat in the low dosage test group. In week 59, a male rat developed squamous cell carcinomaof the fore stomach; this rat had takenBHA at a higher dose.At week 82, a female rat with squamous cell carcinoma of the fore stomach was observed; this female rat had also got the higher dose of the BHA. Many tumors were found in the regionof the fore stomach’s constrained ridge on a gross level. Two or three tumors in the fore stomach were seen in around a third of the rats. In other rats, the tumors were greyish-white, wart-like, or villous nodules with ulceration. Cancer cells were also found to have invaded the lymphatic system. Squamous cell carcinoma has been linked to fibrosarcomatous malignant tissue growth in a few cases. There are two male rats and one female rat who received a higher dose of BHA had lymph node metastases (Ito et al., 1985).

Table.no.1 comparison of food chemical food preservatives.

Conclusion

The current review revealed that the usage of chemical food preservatives in food can cause many severe health problems. The problems that it causeswill depend up on the amount and the durationof the usage of the particular preservative. Some preservative may not act directly but still it may promote or induce many health problems like genotoxicity and carcinogenicity. The study also provided how the preservatives acts, when they induce different health problems and also gives information about health problems are caused by some specific synthetic food preservative. There are studiesgoing on to find properalternates for chemicalpreservatives. The usage of natural preservative in food will help to improve the shelf-life of the food product and the side effects from using it will be a minimum. So, a soft shift from chemical preservative to natural preservative can make a big difference in maintaining good health in the future

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