Monosodium glutamate added to food does not induce damage to the pancreas nor aggravate diabetes due to enhancement of oxidative stress

IF 3.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biochemical and Molecular Toxicology Pub Date : 2024-10-14 DOI:10.1002/jbt.23859
Shintaro Yoshida, Huichia Chao, Asuka Takumi, Masanori Kohmura
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This was attributed to inflammation caused by increased oxidative stress and it was reported that MSG consequently disordered glucose metabolism in healthy rats and aggravated diabetes in STZ-treated rats.<sup>[</sup><span><sup>1</sup></span><sup>]</sup> Finally, it was concluded that not only diabetics, but also healthy people should limit their use of the food additive, MSG. In response to this article, we would like to provide safety information on MSG used as a food additive and comment on these study results.</p><p>MSG is one of the most thoroughly studied food additives. It is well established that glutamate added to foods does not enter the blood circulation nor does the blood glutamate concentration rise when MSG is consumed as part of a normal diet, even when consumed at abnormally high levels.<sup>[</sup><span><sup>2</sup></span><sup>]</sup> Glutamate ingested with food is metabolized as an energy source for enterocytes.<sup>[</sup><span><sup>3, 4</sup></span><sup>]</sup> It has been demonstrated that dietary glutamate is intensively oxidized during the splanchnic first pass in healthy adults and preterm infants.<sup>[</sup><span><sup>5, 6</sup></span><sup>]</sup> A study that investigated the metabolic fate of dietary glutamate (including MSG) showed that almost all dietary glutamate in the rat gut is metabolized into CO2, lactate, alanine or proline (56%, 13%, 12%, 3% of dietary input, respectively).<sup>[</sup><span><sup>7</sup></span><sup>]</sup> Rodent and human studies have also shown that the major nutrients in foods, especially metabolizable carbohydrates, effectively attenuate any rise in blood glutamate levels induced by oral administration of MSG.<sup>[</sup><span><sup>8, 9</sup></span><sup>]</sup> Further studies have shown that the circadian fluctuations in blood glutamate level are not significantly different regardless of whether a diet contains added MSG or not <sup>[</sup><span><sup>10</sup></span><sup>]</sup> and that the basal glutamate level is not affected by long-term MSG consumption.<sup>[</sup><span><sup>11</sup></span><sup>]</sup> The principal conclusion from these studies is that blood glutamate concentration does not rise when MSG is ingested as part of a normal diet even in cases where intake is abnormally high. Considering the results of these studies on the safety of MSG, international scientific committees and regulatory agencies have stated that MSG is safe as a food additive. Since 1958, MSG has been classified by the US Food and Drug Administration as “generally recognized as safe.” The Joint FAO/WHO Expert Committee on Food Additives (JECFA) also evaluated the safety of MSG as a food additive in 1970, 1973, 1987 and as a flavoring agent in 2022.<sup>[</sup><span><sup>12, 13</sup></span><sup>]</sup> Consequently, JECFA concluded that the total dietary intake of glutamate did not represent a health hazard and that it is not necessary to establish a numerically acceptable daily intake for humans, including pregnant women and infants. Until now, JECFA has maintained its safety classification for MSG as “ADI not specified.”</p><p>MSG is the sodium salt of glutamic acid, one of the most abundant naturally occurring non-essential amino acids and a component of protein. Glutamate, along with cystine and glycine, is also known as a precursor of glutathione (GSH), an antioxidant tripeptide which can prevent oxidative damage caused by reactive oxygen species.<sup>[</sup><span><sup>14</sup></span><sup>]</sup> In a piglet study, dietary supplementation with glutamate was shown to alleviate herbicide-induced oxidative stress by enhancing antioxidant capacity, including increased serum superoxide dismutase activity and NO levels and inhibiting MDA generation.<sup>[</sup><span><sup>15</sup></span><sup>]</sup> Another piglet study indicated that dietary supplementation with MSG increased the jejunal concentration of GSH.<sup>[</sup><span><sup>16</sup></span><sup>]</sup> In a mouse study, a 1.3-fold increase in plasma glutamate levels by administration of <span>l</span>-theanine, a precursor of glutamate, together with cystine was reported to significantly increase the total GSH level in the liver.<sup>[</sup><span><sup>17</sup></span><sup>]</sup> In a study using macrophages derived from monocytes, glutamate added to culture medium in the presence of cystine was reported to increase GSH concentration in a dose-dependent manner.<sup>[</sup><span><sup>18</sup></span><sup>]</sup> A human clinical trial also showed that oral supplementation with GSH precursors, consisting of cystine, glutamate and glycine, during the intervention period could potentially increase the level of serum GSH.<sup>[</sup><span><sup>19</sup></span><sup>]</sup> Thus, contrary to the findings of Gelen, et al., these results suggest that elevated Glu levels in the circulation may be able to increase GSH production and enhance antioxidant capacity. This would mean that, even when MSG is administered using a method designed to raise the blood level of glutamate, such as gavage, MSG does not lead to an increase in oxidative stress. Consequently, we find that Gelen, et al.'s assertion that oral administration of MSG increased oxidative stress in the rat pancreas is incompatible with the evidence.</p><p>It should also be noted that when MSG is used as a food additive, it is never given to humans as a bolus in the absence of food. Since MSG is always ingested as an additive with foods, it is clear that the route of administration used in this study (by gavage) is an inappropriate way to investigate the safety of MSG as a food additive. In the OECD guidelines, it is stated that the test substance should be administered by the route most relevant to human exposure. The effects of feeding an MSG-containing diet on healthy and diabetic rats have already been investigated. The study reported that addition of MSG to the diet did not induce any alteration in fasted blood glucose levels, and no significant differences were observed in other biochemical and hematological parameters, as well as liver and kidney histology between control and MSG-fed rats, irrespective of whether the rats were healthy or had diabetes.<sup>[</sup><span><sup>20</sup></span><sup>]</sup> The claim in the Gelen, et al. study that MSG had a harmful effect on the pancreas of healthy and diabetic rats is not consistent with studies conducted under OECD guidelines in a manner more representative of actual exposure. Regarding the association of MSG consumption with glucose metabolism and diabetes in humans, a prospective cohort study to assess the association between MSG consumption and the change in fasting blood glucose levels, including a 5-year follow-up period, was carried out in China. The results indicated that high MSG intake is negatively associated with the incidence of hyperglycemia during the follow-up period and there was a linear inverse association between MSG intake and change in fasting blood glucose levels.<sup>[</sup><span><sup>21</sup></span><sup>]</sup></p><p>Namely, their conclusion that the prevalence of diabetes mellitus might be elevated with increased use of MSG as a seasoning and the use of MSG should be restricted not just in people with diabetes but also in healthy individuals is clearly contradicted by the scientific evidence from human epidemiological and the animal studies conducted under the realistic condition where MSG is used as a food additive. When extrapolating the results of animal studies on food safety to the human population, the difference between study design and actual dietary practice must be taken into consideration, otherwise, the study conclusion will mislead people when making choices about their diet in everyday life. And finally, we can reasonably assert that MSG does not induce any damage to pancreas nor cause poor glycemic control in diabetics when used as a food additive, and consequently there are no safety concerns associated with the use of MSG.</p><p><b>Shintaro Yoshida:</b> Writing original draft; writing review and editing. <b>Huichia Chao:</b> Writing review and editing. <b>Asuka Takumi:</b> Writing review and editing. <b>Masanori Kohmura:</b> Writing review and editing; supervision.</p><p>Shintaro Yoshida, Huichia Chao and Asuka Takumi are the secretariat and Masanori Kohmura is the senior advisor of IGTC, a worldwide research organization having NGO status. The organization carries out or sponsors extensive research on the efficacy, application and safety of glutamic acid and its salts, especially as used in foods. The IGTC receives financial support from glutamate manufacturers and users. Shintaro Yoshida, Huichia Chao, Asuka Takumi and Masanori Kohmura are also employees of Ajinomoto Co., Inc. (Tokyo Japan).</p>","PeriodicalId":15151,"journal":{"name":"Journal of Biochemical and Molecular Toxicology","volume":"38 11","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jbt.23859","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biochemical and Molecular Toxicology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jbt.23859","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

In the article by Gelen, et al. entitled “The investigation of the effects of monosodium glutamate on healthy rat and rats with STZ-induced diabetes,” the authors indicated that oral administration of monosodium glutamate (MSG) at a dose of 30 mg/kg bw/day by gavage for 28 days reduced antioxidative capacity and induced histological abnormalities in the pancreas of healthy rats as well as rats with STZ-induced diabetes. This was attributed to inflammation caused by increased oxidative stress and it was reported that MSG consequently disordered glucose metabolism in healthy rats and aggravated diabetes in STZ-treated rats.[1] Finally, it was concluded that not only diabetics, but also healthy people should limit their use of the food additive, MSG. In response to this article, we would like to provide safety information on MSG used as a food additive and comment on these study results.

MSG is one of the most thoroughly studied food additives. It is well established that glutamate added to foods does not enter the blood circulation nor does the blood glutamate concentration rise when MSG is consumed as part of a normal diet, even when consumed at abnormally high levels.[2] Glutamate ingested with food is metabolized as an energy source for enterocytes.[3, 4] It has been demonstrated that dietary glutamate is intensively oxidized during the splanchnic first pass in healthy adults and preterm infants.[5, 6] A study that investigated the metabolic fate of dietary glutamate (including MSG) showed that almost all dietary glutamate in the rat gut is metabolized into CO2, lactate, alanine or proline (56%, 13%, 12%, 3% of dietary input, respectively).[7] Rodent and human studies have also shown that the major nutrients in foods, especially metabolizable carbohydrates, effectively attenuate any rise in blood glutamate levels induced by oral administration of MSG.[8, 9] Further studies have shown that the circadian fluctuations in blood glutamate level are not significantly different regardless of whether a diet contains added MSG or not [10] and that the basal glutamate level is not affected by long-term MSG consumption.[11] The principal conclusion from these studies is that blood glutamate concentration does not rise when MSG is ingested as part of a normal diet even in cases where intake is abnormally high. Considering the results of these studies on the safety of MSG, international scientific committees and regulatory agencies have stated that MSG is safe as a food additive. Since 1958, MSG has been classified by the US Food and Drug Administration as “generally recognized as safe.” The Joint FAO/WHO Expert Committee on Food Additives (JECFA) also evaluated the safety of MSG as a food additive in 1970, 1973, 1987 and as a flavoring agent in 2022.[12, 13] Consequently, JECFA concluded that the total dietary intake of glutamate did not represent a health hazard and that it is not necessary to establish a numerically acceptable daily intake for humans, including pregnant women and infants. Until now, JECFA has maintained its safety classification for MSG as “ADI not specified.”

MSG is the sodium salt of glutamic acid, one of the most abundant naturally occurring non-essential amino acids and a component of protein. Glutamate, along with cystine and glycine, is also known as a precursor of glutathione (GSH), an antioxidant tripeptide which can prevent oxidative damage caused by reactive oxygen species.[14] In a piglet study, dietary supplementation with glutamate was shown to alleviate herbicide-induced oxidative stress by enhancing antioxidant capacity, including increased serum superoxide dismutase activity and NO levels and inhibiting MDA generation.[15] Another piglet study indicated that dietary supplementation with MSG increased the jejunal concentration of GSH.[16] In a mouse study, a 1.3-fold increase in plasma glutamate levels by administration of l-theanine, a precursor of glutamate, together with cystine was reported to significantly increase the total GSH level in the liver.[17] In a study using macrophages derived from monocytes, glutamate added to culture medium in the presence of cystine was reported to increase GSH concentration in a dose-dependent manner.[18] A human clinical trial also showed that oral supplementation with GSH precursors, consisting of cystine, glutamate and glycine, during the intervention period could potentially increase the level of serum GSH.[19] Thus, contrary to the findings of Gelen, et al., these results suggest that elevated Glu levels in the circulation may be able to increase GSH production and enhance antioxidant capacity. This would mean that, even when MSG is administered using a method designed to raise the blood level of glutamate, such as gavage, MSG does not lead to an increase in oxidative stress. Consequently, we find that Gelen, et al.'s assertion that oral administration of MSG increased oxidative stress in the rat pancreas is incompatible with the evidence.

It should also be noted that when MSG is used as a food additive, it is never given to humans as a bolus in the absence of food. Since MSG is always ingested as an additive with foods, it is clear that the route of administration used in this study (by gavage) is an inappropriate way to investigate the safety of MSG as a food additive. In the OECD guidelines, it is stated that the test substance should be administered by the route most relevant to human exposure. The effects of feeding an MSG-containing diet on healthy and diabetic rats have already been investigated. The study reported that addition of MSG to the diet did not induce any alteration in fasted blood glucose levels, and no significant differences were observed in other biochemical and hematological parameters, as well as liver and kidney histology between control and MSG-fed rats, irrespective of whether the rats were healthy or had diabetes.[20] The claim in the Gelen, et al. study that MSG had a harmful effect on the pancreas of healthy and diabetic rats is not consistent with studies conducted under OECD guidelines in a manner more representative of actual exposure. Regarding the association of MSG consumption with glucose metabolism and diabetes in humans, a prospective cohort study to assess the association between MSG consumption and the change in fasting blood glucose levels, including a 5-year follow-up period, was carried out in China. The results indicated that high MSG intake is negatively associated with the incidence of hyperglycemia during the follow-up period and there was a linear inverse association between MSG intake and change in fasting blood glucose levels.[21]

Namely, their conclusion that the prevalence of diabetes mellitus might be elevated with increased use of MSG as a seasoning and the use of MSG should be restricted not just in people with diabetes but also in healthy individuals is clearly contradicted by the scientific evidence from human epidemiological and the animal studies conducted under the realistic condition where MSG is used as a food additive. When extrapolating the results of animal studies on food safety to the human population, the difference between study design and actual dietary practice must be taken into consideration, otherwise, the study conclusion will mislead people when making choices about their diet in everyday life. And finally, we can reasonably assert that MSG does not induce any damage to pancreas nor cause poor glycemic control in diabetics when used as a food additive, and consequently there are no safety concerns associated with the use of MSG.

Shintaro Yoshida: Writing original draft; writing review and editing. Huichia Chao: Writing review and editing. Asuka Takumi: Writing review and editing. Masanori Kohmura: Writing review and editing; supervision.

Shintaro Yoshida, Huichia Chao and Asuka Takumi are the secretariat and Masanori Kohmura is the senior advisor of IGTC, a worldwide research organization having NGO status. The organization carries out or sponsors extensive research on the efficacy, application and safety of glutamic acid and its salts, especially as used in foods. The IGTC receives financial support from glutamate manufacturers and users. Shintaro Yoshida, Huichia Chao, Asuka Takumi and Masanori Kohmura are also employees of Ajinomoto Co., Inc. (Tokyo Japan).

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添加到食物中的谷氨酸一钠不会对胰腺造成损害,也不会因增强氧化应激而导致糖尿病恶化
在 Gelen 等人题为 "谷氨酸钠对健康大鼠和 STZ 诱导糖尿病大鼠影响的调查 "的文章中,作者指出,以 30 毫克/千克体重/天的剂量灌胃口服谷氨酸钠(MSG)28 天,会降低健康大鼠和 STZ 诱导糖尿病大鼠的抗氧化能力,并诱发胰腺组织学异常。据报道,味精会导致健康大鼠的糖代谢紊乱,并加重 STZ 治疗大鼠的糖尿病。[1] 最后,研究得出结论,不仅糖尿病患者,健康人也应限制使用食品添加剂味精。针对这篇文章,我们想提供有关作为食品添加剂的味精的安全信息,并对这些研究结果发表评论。众所周知,在正常饮食中摄入味精后,添加到食品中的谷氨酸不会进入血液循环,即使摄入量异常高,血液中的谷氨酸浓度也不会升高[2]。[3,4] 研究表明,健康成人和早产儿的膳食谷氨酸钠在脾脏第一次排泄过程中会被大量氧化。[5,6] 一项调查膳食谷氨酸钠(包括味精)代谢去向的研究表明,大鼠肠道中几乎所有的膳食谷氨酸钠都被代谢为二氧化碳、乳酸盐、丙氨酸或脯氨酸(分别占膳食摄入量的 56%、13%、12% 和 3%)。[7] 啮齿类和人类研究还表明,食物中的主要营养成分,特别是可代谢的碳水化合物,可有效缓解口服味精引起的血液谷氨酸含量升高。[8, 9] 进一步的研究表明,无论膳食中是否添加味精,血液中谷氨酸盐含量的昼夜波动都没有显著差异[10],长期食用味精也不会影响谷氨酸盐的基础含量[11]。这些研究的主要结论是,在正常膳食中摄入味精,即使摄入量异常高,血液中谷氨酸盐浓度也不会升高。考虑到这些关于味精安全性的研究结果,国际科学委员会和监管机构已声明味精作为食品添加剂是安全的。自 1958 年以来,味精一直被美国食品和药物管理局归类为 "公认安全"。粮农组织/世卫组织食品添加剂联合专家委员会(JECFA)也于 1970 年、1973 年、1987 年对味精作为食品添加剂的安全性进行了评估,并于 2022 年对味精作为调味剂的安全性进行了评估。[12, 13] 因此,JECFA 得出结论认为,谷氨酸钠的膳食总摄入量不会对健康造成危害,没有必要为人类(包括孕妇和婴儿)制定每日可接受摄入量。直到现在,食品添加剂联合专家委员会仍将味精的安全分类定为 "未指定每日允许摄入量"。味精是谷氨酸的钠盐,谷氨酸是天然存在的最丰富的非必需氨基酸之一,也是蛋白质的组成部分。谷氨酸与胱氨酸和甘氨酸一样,也是谷胱甘肽(GSH)的前体,谷胱甘肽是一种抗氧化三肽,可防止活性氧引起的氧化损伤。[14] 一项仔猪研究表明,膳食中补充谷氨酸可提高抗氧化能力,包括提高血清超氧化物歧化酶活性和 NO 水平,抑制 MDA 的生成,从而缓解除草剂引起的氧化应激。[17]一项使用单核细胞衍生的巨噬细胞进行的研究显示,在胱氨酸存在的情况下,将谷氨酸添加到培养基中会以剂量依赖的方式增加 GSH 的浓度。[18]一项人体临床试验也表明,在干预期间口服由胱氨酸、谷氨酸和甘氨酸组成的 GSH 前体可潜在地提高血清 GSH 水平、因此,与 Gelen 等人的研究结果相反,这些研究结果表明,血液循环中谷氨酸水平的升高可能会增加 GSH 的生成并提高抗氧化能力。这意味着,即使使用旨在提高谷氨酸血药浓度的方法(如灌胃)施用味精,味精也不会导致氧化应激增加。因此,我们认为 Gelen 等人关于口服味精会增加大鼠胰腺氧化应激的说法与证据不符。
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来源期刊
CiteScore
5.80
自引率
2.80%
发文量
277
审稿时长
6-12 weeks
期刊介绍: The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.
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