Pub Date : 2024-11-28eCollection Date: 2024-01-01DOI: 10.1155/jt/6179226
S S S T Fernando, R G P T Jayasooriya, Kalpa W Samarakoon, N D Asha D Wijegunawardana, Sampath B Alahakoon
Research on citrus plants is the result of increasing interest in the discovery of plant species with potential insect-repellent properties. Insect-repelling ability can be achieved by the numerous ubiquitous citrus species. This is mainly due to the presence of phytochemicals such as limonene, citronellol, citral, and α-pinene. These phytochemicals' composition varies depending on the geographical location of the plant. The extraction method dictates the configuration of attainable phytochemicals while the dosage affects the repellency potential. Therefore, developing insect repellent involved a number of observations related to the identification of both citrus plant phytochemical composition present in the different parts of the plant and the repellency potential of these phytochemicals in advance. Conversely, the development of repellent methods that go beyond conventional methods has been made possible by scientific developments including modern strategies such as encapsulation, the preparation of emulsion, and the incorporation of repellents into textiles. Therefore, this review article intends to probe into the aforementioned information and provide a sound insight into citrus-based repellent development in the future.
{"title":"Citrus-Based Bio-Insect Repellents-A Review on Historical and Emerging Trends in Utilizing Phytochemicals of Citrus Plants.","authors":"S S S T Fernando, R G P T Jayasooriya, Kalpa W Samarakoon, N D Asha D Wijegunawardana, Sampath B Alahakoon","doi":"10.1155/jt/6179226","DOIUrl":"10.1155/jt/6179226","url":null,"abstract":"<p><p>Research on citrus plants is the result of increasing interest in the discovery of plant species with potential insect-repellent properties. Insect-repelling ability can be achieved by the numerous ubiquitous citrus species. This is mainly due to the presence of phytochemicals such as limonene, citronellol, citral, and <i>α</i>-pinene. These phytochemicals' composition varies depending on the geographical location of the plant. The extraction method dictates the configuration of attainable phytochemicals while the dosage affects the repellency potential. Therefore, developing insect repellent involved a number of observations related to the identification of both citrus plant phytochemical composition present in the different parts of the plant and the repellency potential of these phytochemicals in advance. Conversely, the development of repellent methods that go beyond conventional methods has been made possible by scientific developments including modern strategies such as encapsulation, the preparation of emulsion, and the incorporation of repellents into textiles. Therefore, this review article intends to probe into the aforementioned information and provide a sound insight into citrus-based repellent development in the future.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"6179226"},"PeriodicalIF":3.4,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11620817/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142785982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
LN19183 is a standardized composition of Citrus aurantifolia (Christm) Swingle (CA) fruit rind and Theobroma cacao L. (TC) seed extracts that have recently been demonstrated to increase resting energy expenditure (REE) and reduce body fat in rats. CA and TC are important herbs in traditional medicine for various health benefits. The present study evaluates the comprehensive toxicity of LN19183 in acute, subchronic, and genetic toxicity studies following the guidelines of the Organization for Economic Co-operation and Development (OECD) for testing chemicals. The acute oral and dermal and 90-day subchronic oral toxicities were performed in rats, and acute dermal and eye irritations were performed in rabbits. In the subchronic toxicity study with a 28-day recovery period, male and female Sprague Dawley rats were orally gavaged with daily LN19183 doses of 500, 1000, or 2000 mg/kg body weight (BW). Furthermore, the genetic toxicity studies included mutagenicity in bacteria, chromosome aberration, and micronucleus assays in human blood mononuclear cells in vitro and micronucleus assay in Swiss albino mice bone marrow in vivo. Acute and subchronic repeat dose oral toxicity studies showed no adverse events, clinical signs, or mortality. All animals exhibited normal food and water intake and natural BW gain. In the 90-day study, LN19183 did not induce major changes in hematology, biochemical evaluations, and urine analysis; gross and histopathological findings did not show any treatment-related lesions or abnormality. The no observed adverse effect level (NOAEL) of LN19183 supplementation was 2000 mg/kg BW/day. In the genetic toxicity studies, LN19183 treatment did not show significant increases in the revertant bacterial colonies, chromosomal aberrations, or number of micronucleated cells. The present observations affirm that oral consumption of LN19183 is safe, and this botanical composition is nonmutagenic and nonclastogenic.
{"title":"Acute, Subchronic, and Genetic Toxicity Assessments of a Composition of <i>Citrus aurantifolia</i> Fruit Rind and <i>Theobroma cacao</i> Seed Extracts.","authors":"Sundararaju Dodda, Sujatha Polavarapu, Krishnaraju Venkata Alluri, Trimurtulu Golakoti, Krishanu Sengupta","doi":"10.1155/jt/4239607","DOIUrl":"10.1155/jt/4239607","url":null,"abstract":"<p><p>LN19183 is a standardized composition of <i>Citrus aurantifolia</i> (Christm) Swingle (CA) fruit rind and <i>Theobroma cacao</i> L. (TC) seed extracts that have recently been demonstrated to increase resting energy expenditure (REE) and reduce body fat in rats. CA and TC are important herbs in traditional medicine for various health benefits. The present study evaluates the comprehensive toxicity of LN19183 in acute, subchronic, and genetic toxicity studies following the guidelines of the Organization for Economic Co-operation and Development (OECD) for testing chemicals. The acute oral and dermal and 90-day subchronic oral toxicities were performed in rats, and acute dermal and eye irritations were performed in rabbits. In the subchronic toxicity study with a 28-day recovery period, male and female Sprague Dawley rats were orally gavaged with daily LN19183 doses of 500, 1000, or 2000 mg/kg body weight (BW). Furthermore, the genetic toxicity studies included mutagenicity in bacteria, chromosome aberration, and micronucleus assays in human blood mononuclear cells in vitro and micronucleus assay in Swiss albino mice bone marrow in vivo. Acute and subchronic repeat dose oral toxicity studies showed no adverse events, clinical signs, or mortality. All animals exhibited normal food and water intake and natural BW gain. In the 90-day study, LN19183 did not induce major changes in hematology, biochemical evaluations, and urine analysis; gross and histopathological findings did not show any treatment-related lesions or abnormality. The no observed adverse effect level (NOAEL) of LN19183 supplementation was 2000 mg/kg BW/day. In the genetic toxicity studies, LN19183 treatment did not show significant increases in the revertant bacterial colonies, chromosomal aberrations, or number of micronucleated cells. The present observations affirm that oral consumption of LN19183 is safe, and this botanical composition is nonmutagenic and nonclastogenic.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"4239607"},"PeriodicalIF":3.4,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11617045/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142780347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-22eCollection Date: 2024-01-01DOI: 10.1155/jt/9425206
Mathewos Temesgen, Tegenu Alemu, Enkosa Shasho
This study aimed to determine the levels of some heavy metals in the Koche River and the potential health risks. A replica of water samples was taken from 12 sampling sites purposely selected in the dry season. Heavy metal levels were determined using a flame atomic absorption spectrophotometer following the APHA (1998) procedure. Heavy metal pollution index (HPI), heavy metal evaluation index (HEI), chronic daily intake (CDI), hazard quotient (HQ), hazard index (HI), total hazard index (THI), and incremental lifetime cancer risk were calculated on the basis of the results. The heavy metals detected were Fe > Mn > Cu > Zn > Cr. The Cr, Fe, Mn, and Cu contents were above the maximum allowed limit of WHO for drinking and irrigation water at most of the sampling sites. The HPI and HEI values also surpassed the maximum limit of the study sites. The highest HPI and HEI values were found at the Yam1site. Oral ingestion represented 99.55% and 97.85% of CDItotal (CDIingestion + CDIdermal contact) in adults and children, respectively. The mean CDItotal and the noncarcinogenic risk values were found in the order of Fe > Mn > Cu > Zn > Cr in both ages. CDI, HQ, HI, and THI scores were higher in children. The HIoral and THI values were also higher than 1 in both ages except in DK 2, Sour 1, and Sour 2 sites. However, the HQdermal level was higher than 1 only for Cr in children. The ELCR obtained also indicated a high carcinogenic risk of Cr (0.75 ± 0.44 and 1.15 ± 0.66 in adults and children, respectively). In general, most of the study sites had heavy metal pollution levels that exceeded the maximum allowed limit. Therefore, effective management of sources of pollution and continuous monitoring of river quality to minimize health risks are very important.
本研究旨在确定科切河中某些重金属的含量及其潜在的健康风险。在旱季特意选择了12个采样点,复制了水样。根据APHA(1998)程序,使用火焰原子吸收分光光度计测定重金属水平。据此计算重金属污染指数(HPI)、重金属评价指数(HEI)、慢性日摄入量(CDI)、危害商(HQ)、危害指数(HI)、总危害指数(THI)和终生递增癌症风险。检测到的重金属有Fe > Mn > Cu > Zn > Cr。大部分采样点饮用水和灌溉水的Cr、Fe、Mn、Cu含量均高于WHO规定的最高限量。HPI和HEI值也超过了研究点的最大值。HPI和HEI值在yam1位点最高。口服摄入分别占成人和儿童cdi总量(cdi摄入+皮肤接触)的99.55%和97.85%。两个年龄段的平均cdtotal和非致癌风险值依次为Fe > Mn > Cu > Zn > Cr。儿童的CDI、HQ、HI和THI评分较高。除2号、1号和2号位点外,2个年龄段的HIoral和THI值均高于1。然而,HQdermal水平高于1的只有儿童的Cr。获得的ELCR也表明铬的高致癌风险(成人和儿童分别为0.75±0.44和1.15±0.66)。总的来说,大多数研究地点的重金属污染水平超过了最大允许限度。因此,有效管理污染源和持续监测河流质量,以尽量减少健康风险是非常重要的。
{"title":"Heavy Metals Pollution and Potential Health Risks: The Case of the Koche River, Tatek Industrial Zone, Burayu, Ethiopia.","authors":"Mathewos Temesgen, Tegenu Alemu, Enkosa Shasho","doi":"10.1155/jt/9425206","DOIUrl":"https://doi.org/10.1155/jt/9425206","url":null,"abstract":"<p><p>This study aimed to determine the levels of some heavy metals in the Koche River and the potential health risks. A replica of water samples was taken from 12 sampling sites purposely selected in the dry season. Heavy metal levels were determined using a flame atomic absorption spectrophotometer following the APHA (1998) procedure. Heavy metal pollution index (HPI), heavy metal evaluation index (HEI), chronic daily intake (CDI), hazard quotient (HQ), hazard index (HI), total hazard index (THI), and incremental lifetime cancer risk were calculated on the basis of the results. The heavy metals detected were Fe > Mn > Cu > Zn > Cr. The Cr, Fe, Mn, and Cu contents were above the maximum allowed limit of WHO for drinking and irrigation water at most of the sampling sites. The HPI and HEI values also surpassed the maximum limit of the study sites. The highest HPI and HEI values were found at the Yam1site. Oral ingestion represented 99.55% and 97.85% of CDI<sub>total</sub> (CDI<sub>ingestion</sub> + CDI<sub>dermal</sub> contact) in adults and children, respectively. The mean CDI<sub>total</sub> and the noncarcinogenic risk values were found in the order of Fe > Mn > Cu > Zn > Cr in both ages. CDI, HQ, HI, and THI scores were higher in children. The HI<sub>oral</sub> and THI values were also higher than 1 in both ages except in DK 2, Sour 1, and Sour 2 sites. However, the HQ<sub>dermal</sub> level was higher than 1 only for Cr in children. The ELCR obtained also indicated a high carcinogenic risk of Cr (0.75 ± 0.44 and 1.15 ± 0.66 in adults and children, respectively). In general, most of the study sites had heavy metal pollution levels that exceeded the maximum allowed limit. Therefore, effective management of sources of pollution and continuous monitoring of river quality to minimize health risks are very important.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"9425206"},"PeriodicalIF":3.4,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11608300/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142769977","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-12eCollection Date: 2024-01-01DOI: 10.1155/2024/6197553
Ogechukwu E Ezim, Lilian Kidi, Lauritta C Ndufeiya-Kumasi, Sunny O Abarikwu
The protective effect of Fe against Cd-induced toxicity in the liver and kidney of rats during concurrent administration of both metals was investigated in this study. Fifty female rats (130-150 g) were distributed into five groups of 10 rats each (n = 10): Group I (control), received normal saline solution; Group II (1.2 mg CdCl2/kg b.w.); Group III (1.2 mg CdCl2 + 0.25 mg FeCl2/kg b.w.); Group IV (1.2 mg CdCl2 + 0.75 mg FeCl2/kg b.w.); and Group V (1.2 mg CdCl2 + 1.5 mg FeCl2/kg b.w.). Administration of both tested substances lasted for 47 days. Cd was injected intraperitoneally once a week, while Fe was administered to the Cd-exposed animals by oral gavage thrice weekly. The animals were killed at the end of the study, their blood was collected, and their liver and kidneys were harvested for biochemical and histological analysis. Following Cd administration, the kidney and liver showed a significant increase in Cd concentration, while Fe concentration in the kidney decreased. However, cotreatment with Fe decreased Cd concentration in the kidney and liver and increased Fe concentration in the kidney but not the liver, and the effect was more pronounced in the higher than lower doses. In the kidney, cotreatment with Fe especially at higher doses inhibited Cd-induced lipid peroxidation and plasma uric acid concentration. In the liver, lipid peroxidation which Cd did not alter was found to be elevated after cotreatment with the highest dose Fe. Inflammatory cell infiltrations of the central vein and renal tubular and glomeruli injury induced by Cd were not obviated by Fe cotreatment. It seems that both tissues respond differently to the concurrent administration of these metals and that Fe protected the kidney against oxidative injury-induced by Cd but not histopathological changes in both tissues.
{"title":"Iron Administration Partially Ameliorates Cadmium-Induced Oxidative Damage in the Liver and Kidney of Rats.","authors":"Ogechukwu E Ezim, Lilian Kidi, Lauritta C Ndufeiya-Kumasi, Sunny O Abarikwu","doi":"10.1155/2024/6197553","DOIUrl":"10.1155/2024/6197553","url":null,"abstract":"<p><p>The protective effect of Fe against Cd-induced toxicity in the liver and kidney of rats during concurrent administration of both metals was investigated in this study. Fifty female rats (130-150 g) were distributed into five groups of 10 rats each (<i>n</i> = 10): Group I (control), received normal saline solution; Group II (1.2 mg CdCl<sub>2</sub>/kg b.w.); Group III (1.2 mg CdCl<sub>2</sub> + 0.25 mg FeCl<sub>2</sub>/kg b.w.); Group IV (1.2 mg CdCl<sub>2</sub> + 0.75 mg FeCl<sub>2</sub>/kg b.w.); and Group V (1.2 mg CdCl<sub>2</sub> + 1.5 mg FeCl<sub>2</sub>/kg b.w.). Administration of both tested substances lasted for 47 days. Cd was injected intraperitoneally once a week, while Fe was administered to the Cd-exposed animals by oral gavage thrice weekly. The animals were killed at the end of the study, their blood was collected, and their liver and kidneys were harvested for biochemical and histological analysis. Following Cd administration, the kidney and liver showed a significant increase in Cd concentration, while Fe concentration in the kidney decreased. However, cotreatment with Fe decreased Cd concentration in the kidney and liver and increased Fe concentration in the kidney but not the liver, and the effect was more pronounced in the higher than lower doses. In the kidney, cotreatment with Fe especially at higher doses inhibited Cd-induced lipid peroxidation and plasma uric acid concentration. In the liver, lipid peroxidation which Cd did not alter was found to be elevated after cotreatment with the highest dose Fe. Inflammatory cell infiltrations of the central vein and renal tubular and glomeruli injury induced by Cd were not obviated by Fe cotreatment. It seems that both tissues respond differently to the concurrent administration of these metals and that Fe protected the kidney against oxidative injury-induced by Cd but not histopathological changes in both tissues.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"6197553"},"PeriodicalIF":3.4,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11576088/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142676132","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction:Urtica simensis has been used to treat various diseases such as malaria, hypertension, diabetes, gonorrhea, gastritis, body swelling, and wound infections. However, the safety of consuming U. simensis leaves during pregnancy has not been evaluated yet. Therefore, this experimental study was conducted to evaluate the toxic effects of U. simensis leaf extract on the prenatal development of embryos and fetuses in pregnant rats. Methods: Fifty pregnant Wistar albino rats were randomly assigned to five groups of 10 gravid rats for each experiment. Groups I-III were given 70% ethanol leaf extract of U. simensis at doses of 250, 500, and 1000 mg/kg daily from 6th to 12th days of gestation. Groups IV-V were kept as pair-fed and ad libitum controls. The developing embryos and fetuses were retrieved on 12 days and 20 days of gestation, respectively. Embryos were evaluated for growth and developmental delays. Fetuses were also assessed for growth retardation and external and visceral anomalies. Results: In the embryonic experiment, somite numbers (p=0.001) and morphological scores (p=0.029) were significantly decreased in pregnant rats given 1000 mg/kg of U. simensis leaf extract. Embryonic developments of the caudal neural tube (CNT) (p=0.001), otic system (p=0.025), olfactory system (p=0.013), and limb buds (p=0.026) were significantly delayed in pregnant rats given 1000 mg/kg of extract. Oral administration of 500 mg/kg of U. simensis leaf extract also caused significant developmental delays in the CNT (p=0.021) and olfactory system (p=0.032). In the fetal experiment, fetal resorption (p=0.015) was significantly increased whereas crown rump length (p=0.012) and fetal weight (p=0.019) were significantly decreased in pregnant rats given 1000 mg/kg of U. simensis leaf extract. Conclusions: The embryotoxic effects of U. simensis leaf extract were evidenced by significant developmental delays. The fetal toxic effects of U. simensis leaf extract were also shown by significant decreases in fetal growth indices. Therefore, pregnant women should be well informed of the possible toxic effects of consuming U. simensis leaf during pregnancy.
简介:荨麻被用于治疗各种疾病,如疟疾、高血压、糖尿病、淋病、胃炎、身体肿胀和伤口感染。然而,在怀孕期间食用荨麻叶的安全性尚未得到评估。因此,本实验研究旨在评估 U. simensis 叶提取物对怀孕大鼠胚胎和胎儿产前发育的毒性影响。研究方法将 50 只怀孕的 Wistar 白化大鼠随机分为 5 组,每组 10 只。第 I 至第 III 组在妊娠期第 6 至第 12 天每天服用 70% 的 U. simensis 乙醇叶提取物,剂量分别为 250、500 和 1000 毫克/千克。第 IV 至第 V 组为配对喂养和自由饮食对照组。分别在妊娠 12 天和 20 天取出发育中的胚胎和胎儿。对胚胎的生长和发育迟缓进行评估。还对胎儿的生长迟缓、外部和内脏异常进行了评估。结果在胚胎实验中,服用 1000 毫克/千克 U. simensis 叶提取物的妊娠大鼠体节数(p=0.001)和形态评分(p=0.029)显著下降。给予 1000 毫克/千克提取物的妊娠大鼠尾神经管(CNT)(p=0.001)、耳系统(p=0.025)、嗅觉系统(p=0.013)和肢芽(p=0.026)的胚胎发育明显延迟。口服 500 毫克/千克 U. simensis 叶提取物也会导致中枢神经系统(p=0.021)和嗅觉系统(p=0.032)发育明显延迟。在胎儿实验中,服用 1000 毫克/千克 U. simensis 叶提取物的妊娠大鼠的胎儿再吸收(p=0.015)显著增加,而冠臀长(p=0.012)和胎儿体重(p=0.019)则显著减少。结论U. simensis叶提取物的胚胎毒性作用表现为明显的发育迟缓。U. simensis叶提取物对胎儿的毒性作用还表现为胎儿生长指数的显著下降。因此,孕妇应充分了解怀孕期间食用 U. simensis 叶可能产生的毒性影响。
{"title":"Embryo and Fetal Toxic Effects of the Hydroethanol Extract of <i>Urtica simensis</i> Hochst. Ex. A. Rich Leaves in Pregnant Rats.","authors":"Bickes Wube, Kaleab Asres, Samuel Woldekidan, Abiy Abebe, Yonas Girma, Girma Seyoum","doi":"10.1155/2024/9986648","DOIUrl":"10.1155/2024/9986648","url":null,"abstract":"<p><p><b>Introduction:</b> <i>Urtica simensis</i> has been used to treat various diseases such as malaria, hypertension, diabetes, gonorrhea, gastritis, body swelling, and wound infections. However, the safety of consuming <i>U. simensis</i> leaves during pregnancy has not been evaluated yet. Therefore, this experimental study was conducted to evaluate the toxic effects of <i>U. simensis</i> leaf extract on the prenatal development of embryos and fetuses in pregnant rats. <b>Methods:</b> Fifty pregnant Wistar albino rats were randomly assigned to five groups of 10 gravid rats for each experiment. Groups I-III were given 70% ethanol leaf extract of <i>U. simensis</i> at doses of 250, 500, and 1000 mg/kg daily from 6<sup>th</sup> to 12<sup>th</sup> days of gestation. Groups IV-V were kept as pair-fed and ad libitum controls. The developing embryos and fetuses were retrieved on 12 days and 20 days of gestation, respectively. Embryos were evaluated for growth and developmental delays. Fetuses were also assessed for growth retardation and external and visceral anomalies. <b>Results:</b> In the embryonic experiment, somite numbers (<i>p</i>=0.001) and morphological scores (<i>p</i>=0.029) were significantly decreased in pregnant rats given 1000 mg/kg of <i>U. simensis</i> leaf extract. Embryonic developments of the caudal neural tube (CNT) (<i>p</i>=0.001), otic system (<i>p</i>=0.025), olfactory system (<i>p</i>=0.013), and limb buds (<i>p</i>=0.026) were significantly delayed in pregnant rats given 1000 mg/kg of extract. Oral administration of 500 mg/kg of <i>U. simensis</i> leaf extract also caused significant developmental delays in the CNT (<i>p</i>=0.021) and olfactory system (<i>p</i>=0.032). In the fetal experiment, fetal resorption (<i>p</i>=0.015) was significantly increased whereas crown rump length (<i>p</i>=0.012) and fetal weight (<i>p</i>=0.019) were significantly decreased in pregnant rats given 1000 mg/kg of <i>U. simensis</i> leaf extract. <b>Conclusions:</b> The embryotoxic effects of <i>U. simensis</i> leaf extract were evidenced by significant developmental delays. The fetal toxic effects of <i>U. simensis</i> leaf extract were also shown by significant decreases in fetal growth indices. Therefore, pregnant women should be well informed of the possible toxic effects of consuming <i>U. simensis</i> leaf during pregnancy.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"9986648"},"PeriodicalIF":3.4,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11567719/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142648372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-30eCollection Date: 2024-01-01DOI: 10.1155/2024/5698516
Danladi Chiroma Husaini, Rodeli Kaylin Mendez, Michael Arzu, Lydia Harris-Thurton
Background: The global spread and accumulation of plastics in freshwater, marine, and terrestrial settings are of great concern to public health and the environment, especially in developing countries with few resources. In the Caribbean and Latin America, nearly 17,000 tons of plastic waste are generated and trashed daily in open dumpsites with attendant consequences for the environment, the economy, aquatic life, the beauty of sea beaches, and public health. The increased use of plastics threatens public health and the ecosystem. Main Body. This systematic review assessed the impact of plastic waste on the environment, economy, and public health in LAC by searching relevant databases such as PubMed, HINARI, Google Scholar, and Scopus. PRISMA and Rayyan software were used to select and analyze research articles for the review.
Conclusions: The review showed that plastic pollution significantly impacts the environment, aquatic life, economy, and human health in LAC. The review further indicated that countries in LAC are working assiduously to address the issues associated with plastic pollution. The use of biodegradable plastics, cleanup campaigns, and policies/programs to reduce or ban plastics are some current efforts in many LAC countries. More research on the impact of plastic waste needs to be conducted, especially in the Caribbean, to address and mitigate the challenges of plastic pollution.
{"title":"Plastic Waste in Latin America and the Caribbean (LAC): Impact on the Environment and Public Health-A Systematic Review.","authors":"Danladi Chiroma Husaini, Rodeli Kaylin Mendez, Michael Arzu, Lydia Harris-Thurton","doi":"10.1155/2024/5698516","DOIUrl":"https://doi.org/10.1155/2024/5698516","url":null,"abstract":"<p><strong>Background: </strong>The global spread and accumulation of plastics in freshwater, marine, and terrestrial settings are of great concern to public health and the environment, especially in developing countries with few resources. In the Caribbean and Latin America, nearly 17,000 tons of plastic waste are generated and trashed daily in open dumpsites with attendant consequences for the environment, the economy, aquatic life, the beauty of sea beaches, and public health. The increased use of plastics threatens public health and the ecosystem. <i>Main Body</i>. This systematic review assessed the impact of plastic waste on the environment, economy, and public health in LAC by searching relevant databases such as PubMed, HINARI, Google Scholar, and Scopus. PRISMA and Rayyan software were used to select and analyze research articles for the review.</p><p><strong>Conclusions: </strong>The review showed that plastic pollution significantly impacts the environment, aquatic life, economy, and human health in LAC. The review further indicated that countries in LAC are working assiduously to address the issues associated with plastic pollution. The use of biodegradable plastics, cleanup campaigns, and policies/programs to reduce or ban plastics are some current efforts in many LAC countries. More research on the impact of plastic waste needs to be conducted, especially in the Caribbean, to address and mitigate the challenges of plastic pollution.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"5698516"},"PeriodicalIF":3.4,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11458288/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142391517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-29eCollection Date: 2024-01-01DOI: 10.1155/2024/5261994
Prakriti Sharma, R S Sethi
Deltamethrin is an insecticide used to control harmful agricultural insects that otherwise damage crops and to control vector-borne diseases. Long-term exposure to deltamethrin results in the inflammation of the lungs. The present study elucidates the molecular mechanism underlying the deltamethrin-induced lung damage. The lung samples were extracted from the Swiss albino mice following the treatment of low (2.5 mg/kg) and high (5 mg/kg) doses of deltamethrin. The mRNA expression of TCR, IL-4, and IL-13 showed upregulation, while the expression of NFAT and FOS was downregulated following a low dose of deltamethrin. Moreover, the expression of TCR was downregulated with the exposure of a high dose of deltamethrin. Furthermore, the immunohistochemistry data confirmed the pattern of protein expression for TCR, FOS, IL-4, and IL-13 following a low dose of deltamethrin exposure. However, no change was seen in the TCR, NFAT, FOS, JUN, IL-4, and IL-13 immunopositive cells of the high-dose treatment group. Also, ELISA results showed increased expression of IL-13 in the BAL fluid of animals exposed to low doses of deltamethrin. Overall, the present study showed that deltamethrin exposure induces lung damage and immune dysregulation via dysregulating the NFAT signalling pathway.
{"title":"<i>In Vivo</i> Exposure of Deltamethrin Dysregulates the NFAT Signalling Pathway and Induces Lung Damage.","authors":"Prakriti Sharma, R S Sethi","doi":"10.1155/2024/5261994","DOIUrl":"10.1155/2024/5261994","url":null,"abstract":"<p><p>Deltamethrin is an insecticide used to control harmful agricultural insects that otherwise damage crops and to control vector-borne diseases. Long-term exposure to deltamethrin results in the inflammation of the lungs. The present study elucidates the molecular mechanism underlying the deltamethrin-induced lung damage. The lung samples were extracted from the Swiss albino mice following the treatment of low (2.5 mg/kg) and high (5 mg/kg) doses of deltamethrin. The mRNA expression of TCR, IL-4, and IL-13 showed upregulation, while the expression of NFAT and FOS was downregulated following a low dose of deltamethrin. Moreover, the expression of TCR was downregulated with the exposure of a high dose of deltamethrin. Furthermore, the immunohistochemistry data confirmed the pattern of protein expression for TCR, FOS, IL-4, and IL-13 following a low dose of deltamethrin exposure. However, no change was seen in the TCR, NFAT, FOS, JUN, IL-4, and IL-13 immunopositive cells of the high-dose treatment group. Also, ELISA results showed increased expression of IL-13 in the BAL fluid of animals exposed to low doses of deltamethrin. Overall, the present study showed that deltamethrin exposure induces lung damage and immune dysregulation via dysregulating the NFAT signalling pathway.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"5261994"},"PeriodicalIF":3.0,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11377118/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142140430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-27eCollection Date: 2024-01-01DOI: 10.1155/2024/5539386
Ahmed Saeed Kabbashi, Salwa Abdulla Eltawaty, Amar Mohamed Ismail, Ahmed Abdelhhafiz Elshikh, Ayat Ahmed Alrasheid, Rawan Ahmed Elmahi, Waleed S Koko, Elbadri Elamin Osman
Objective: To investigate the antioxidant and hepatoprotective effects of ethanolic Mangifera indica (M. indica) seed extract on carbon tetrachloride (CCl4)-induced hepatotoxicity in albino rats.
Methods: Forty-eight albino rats weighing (100-150 g) were used for hepatoprotective and toxicity experiments. Antioxidant activity was determined using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. The toxicity of M. indica seeds on the liver was evaluated by examining wellness parameters, body weight, and liver histological sections. The protective effects of 50 mg/kg and 100 mg/kg of seed extract on CCl4-induced hepatotoxicity were investigated by evaluating hematological, renal, and liver function parameters, body weight, and liver histological sections.
Results: The antioxidant activity of the M. indica ethanolic extract was (92 ± 0.03 RSA %) compared with (91 ± 0.01 RSA %) of propyl gallate, and the IC50 was (8.3 ± 0.01 µg/ml) and (14.1 ± 0.01 µg/ml). No changes were observed in the health indicators, body weights, and liver histological sections following oral administration of 50 mg/kg and 100 mg/kg of M. indica seed extracts. Treatment with M. indica seed extract significantly reduced alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), blood sugar, and urea levels compared with those in the CCl4-treated group.
Conclusion: The IC50 of the M. indica ethanolic extract was 8.3 µg/ml, and the M. indica extract is a potential source of natural antioxidants that protect against CCl4-induced hepatotoxicity.
{"title":"Ethanolic Extract of <i>Mangifera indica</i> Protects against CCl<sub>4</sub>-Induced Hepatotoxicity via Antioxidant Capabilities in Albino Rats.","authors":"Ahmed Saeed Kabbashi, Salwa Abdulla Eltawaty, Amar Mohamed Ismail, Ahmed Abdelhhafiz Elshikh, Ayat Ahmed Alrasheid, Rawan Ahmed Elmahi, Waleed S Koko, Elbadri Elamin Osman","doi":"10.1155/2024/5539386","DOIUrl":"10.1155/2024/5539386","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the antioxidant and hepatoprotective effects of ethanolic <i>Mangifera indica</i> (<i>M. indica</i>) seed extract on carbon tetrachloride (CCl<sub>4</sub>)-induced hepatotoxicity in albino rats.</p><p><strong>Methods: </strong>Forty-eight albino rats weighing (100-150 g) were used for hepatoprotective and toxicity experiments. Antioxidant activity was determined using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. The toxicity of <i>M. indica</i> seeds on the liver was evaluated by examining wellness parameters, body weight, and liver histological sections. The protective effects of 50 mg/kg and 100 mg/kg of seed extract on CCl<sub>4</sub>-induced hepatotoxicity were investigated by evaluating hematological, renal, and liver function parameters, body weight, and liver histological sections.</p><p><strong>Results: </strong>The antioxidant activity of the <i>M. indica</i> ethanolic extract was (92 ± 0.03 RSA %) compared with (91 ± 0.01 RSA %) of propyl gallate, and the IC<sub>50</sub> was (8.3 ± 0.01 <i>µ</i>g/ml) and (14.1 ± 0.01 <i>µ</i>g/ml). No changes were observed in the health indicators, body weights, and liver histological sections following oral administration of 50 mg/kg and 100 mg/kg of <i>M. indica</i> seed extracts. Treatment with <i>M. indica</i> seed extract significantly reduced alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), blood sugar, and urea levels compared with those in the CCl<sub>4</sub>-treated group.</p><p><strong>Conclusion: </strong>The IC<sub>50</sub> of the <i>M. indica</i> ethanolic extract was 8.3 <i>µ</i>g/ml, and the <i>M. indica</i> extract is a potential source of natural antioxidants that protect against CCl<sub>4</sub>-induced hepatotoxicity.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"5539386"},"PeriodicalIF":3.4,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11371441/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142126087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-09eCollection Date: 2024-01-01DOI: 10.1155/2024/2970470
Yulma Lizbeth Aguirre-García, Ainara Castillo-Manzanares, Lissethe Palomo-Ligas, Juan Alberto Ascacio-Valdés, Lizeth Guadalupe Campos-Múzquiz, Sandra Cecilia Esparza-González, Raúl Rodríguez-Herrera, Sendar Daniel Nery-Flores
Flourensia cernua DC, commonly known as hojasen or tarbush, is a medicinal plant used in arid regions due to its therapeutic properties, especially in the treatment of gastrointestinal disorders. This study aimed to assess the toxicity of a polyphenolic extract obtained from F. cernua. This research involved both in vitro (hemolytic and brine shrimp assay) and in vivo tests (acute oral toxicity) to determine the safety profile of this extract. The extract was obtained through a novel ultrasound-microwave extraction and purified by ion-exchange chromatography. Analysis of the polyphenolic extract revealed a rich composition of flavonoids and hydroxycinnamic acids, mainly apigenin glycosides. In toxicity tests, the polyphenols did not exhibit toxicity towards Artemia salina at a concentration of 1 mg/ml. Furthermore, incubation at 500 μg/ml for 4 hours showed a slight toxic effect on erythrocytes. In the acute oral toxicity test in mice, doses of 300 mg/kg and 2000 mg/kg did not result in animal mortality, indicating that the LD50 exceeds 2000 mg/kg. However, the higher dose induced signs of toxicity, including lethargy, drowsiness, piloerection, and a significant decrease in weight during the initial two days postadministration of the polyphenolic extract. In addition, histological analysis suggested potential kidney damage at the 2000 mg/kg dose. According to OECD guidelines, while the extract can be classified as category 5 (low acute toxicity) due to the absence of mortality at 2000 mg/kg, the observed signs of toxicity should be considered in the overall risk assessment. These findings highlight the potential of F. cernua in pharmaceutical and nutraceutical applications due to its high polyphenolic content. However, further investigations are necessary to explore the specific effects of the compounds present in the extract. In addition, continuous evaluation of its long-term toxicity is essential to fully understand the extract's safety profile and efficacy.
{"title":"Toxicity Evaluation of a Polyphenolic Extract from <i>Flourensia cernua</i> DC through <i>Artemia</i> Lethality Assay, Hemolytic Activity, and Acute Oral Test.","authors":"Yulma Lizbeth Aguirre-García, Ainara Castillo-Manzanares, Lissethe Palomo-Ligas, Juan Alberto Ascacio-Valdés, Lizeth Guadalupe Campos-Múzquiz, Sandra Cecilia Esparza-González, Raúl Rodríguez-Herrera, Sendar Daniel Nery-Flores","doi":"10.1155/2024/2970470","DOIUrl":"10.1155/2024/2970470","url":null,"abstract":"<p><p><i>Flourensia cernua</i> DC, commonly known as hojasen or tarbush, is a medicinal plant used in arid regions due to its therapeutic properties, especially in the treatment of gastrointestinal disorders. This study aimed to assess the toxicity of a polyphenolic extract obtained from <i>F. cernua</i>. This research involved both <i>in vitro</i> (hemolytic and brine shrimp assay) and <i>in vivo</i> tests (acute oral toxicity) to determine the safety profile of this extract. The extract was obtained through a novel ultrasound-microwave extraction and purified by ion-exchange chromatography. Analysis of the polyphenolic extract revealed a rich composition of flavonoids and hydroxycinnamic acids, mainly apigenin glycosides. In toxicity tests, the polyphenols did not exhibit toxicity towards <i>Artemia salina</i> at a concentration of 1 mg/ml. Furthermore, incubation at 500 <i>μ</i>g/ml for 4 hours showed a slight toxic effect on erythrocytes. In the acute oral toxicity test in mice, doses of 300 mg/kg and 2000 mg/kg did not result in animal mortality, indicating that the LD<sub>50</sub> exceeds 2000 mg/kg. However, the higher dose induced signs of toxicity, including lethargy, drowsiness, piloerection, and a significant decrease in weight during the initial two days postadministration of the polyphenolic extract. In addition, histological analysis suggested potential kidney damage at the 2000 mg/kg dose. According to OECD guidelines, while the extract can be classified as category 5 (low acute toxicity) due to the absence of mortality at 2000 mg/kg, the observed signs of toxicity should be considered in the overall risk assessment. These findings highlight the potential of <i>F. cernua</i> in pharmaceutical and nutraceutical applications due to its high polyphenolic content. However, further investigations are necessary to explore the specific effects of the compounds present in the extract. In addition, continuous evaluation of its long-term toxicity is essential to fully understand the extract's safety profile and efficacy.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"2970470"},"PeriodicalIF":3.4,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11329308/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142000294","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-06eCollection Date: 2024-01-01DOI: 10.1155/2024/1643693
Saud D AlOtaibi, Hossam A Elsisi, Mohammed J AlShammary, Saud A AlQader, Hejab A AlHarbi, Bayan R AlOlaiyan, Ahmad O Alanazi, Firas S AlMendeel, Yazeed N AlHarbi, Ibrahim AlKhalaf, Ahmad H Alhowail, Abdelhamid Mohamed Elwy, Ashraf M Emara
Background: People who are addicted to amphetamines have a much greater chance of developing psychosis compared to those who are not. It is essential to study the behavioral and psychological effects of amphetamines. Therefore, this research aimed to examine conditions such as depression, anxiety, mood, cognitive abilities at the workplace, and social responsibilities by using sociodemographic factors as useful tools in determining effective strategies for preventing, managing, and treating amphetamine addiction.
Methods: A cross-sectional study among addicts hospitalized at two rehabilitation centers across Saudi Arabia between May and October 2023. A validated questionnaire consisting of psychiatric disorders assessment tools was distributed to healthcare professionals to start an interview with addicts to assess the abnormalities. The results were compared with healthy people (control). The assessment tools used are Hamilton Anxiety and Depression Rating Scale, Young Mania Rating Scale, and Work and Social Adjustment Scale. The data were analyzed using SPSS version 22.0. Pearson correlation coefficients (r) were employed.
Results: A total of 60 subjects participated in this study. The participants were divided into two groups (n = 60): group I was control (n = 25) healthy volunteers and group II was amphetamine abusers (n = 35), who were hospitalized for detoxification. The ages ranged from 18 to 60 years old with mean ages of 38.68 (±8.14) and 37.77 (±10.95) years in the control and amphetamine groups, respectively. Among the addicts, the mean severity dependence scale value was 10.46 (±1.82), which denotes high dependency on the illicit drug. The prevalence of high levels of anxiety, depression, and bipolar disorder was significantly higher among addicts when they were compared to healthy people (control). The assessment of the Work and Social Adjustment Scale (WSAS) reflected a higher impairment that minimized their ability to perform the work requirements, home management, social leisure, and relationships.
Conclusions: The addiction to amphetamines was associated with high impairment of work performance and social obligations and a negative impact on the addict's mental health. The risk of suffering anxiety, depression, and bipolar is higher than in nonaddict people. These effects are attributed to brain damage, neurotoxicity, and neuronal inflammation, particularly when these substances are abused over extended periods and at higher doses.
{"title":"Evaluation of the Psychiatric Disorders among Amphetamine Addicts in Rehabilitation Centers: A Cross-Sectional Analysis.","authors":"Saud D AlOtaibi, Hossam A Elsisi, Mohammed J AlShammary, Saud A AlQader, Hejab A AlHarbi, Bayan R AlOlaiyan, Ahmad O Alanazi, Firas S AlMendeel, Yazeed N AlHarbi, Ibrahim AlKhalaf, Ahmad H Alhowail, Abdelhamid Mohamed Elwy, Ashraf M Emara","doi":"10.1155/2024/1643693","DOIUrl":"10.1155/2024/1643693","url":null,"abstract":"<p><strong>Background: </strong>People who are addicted to amphetamines have a much greater chance of developing psychosis compared to those who are not. It is essential to study the behavioral and psychological effects of amphetamines. Therefore, this research aimed to examine conditions such as depression, anxiety, mood, cognitive abilities at the workplace, and social responsibilities by using sociodemographic factors as useful tools in determining effective strategies for preventing, managing, and treating amphetamine addiction.</p><p><strong>Methods: </strong>A cross-sectional study among addicts hospitalized at two rehabilitation centers across Saudi Arabia between May and October 2023. A validated questionnaire consisting of psychiatric disorders assessment tools was distributed to healthcare professionals to start an interview with addicts to assess the abnormalities. The results were compared with healthy people (control). The assessment tools used are Hamilton Anxiety and Depression Rating Scale, Young Mania Rating Scale, and Work and Social Adjustment Scale. The data were analyzed using SPSS version 22.0. Pearson correlation coefficients (<i>r</i>) were employed.</p><p><strong>Results: </strong>A total of 60 subjects participated in this study. The participants were divided into two groups (<i>n</i> = 60): group I was control (<i>n</i> = 25) healthy volunteers and group II was amphetamine abusers (<i>n</i> = 35), who were hospitalized for detoxification. The ages ranged from 18 to 60 years old with mean ages of 38.68 (±8.14) and 37.77 (±10.95) years in the control and amphetamine groups, respectively. Among the addicts, the mean severity dependence scale value was 10.46 (±1.82), which denotes high dependency on the illicit drug. The prevalence of high levels of anxiety, depression, and bipolar disorder was significantly higher among addicts when they were compared to healthy people (control). The assessment of the Work and Social Adjustment Scale (WSAS) reflected a higher impairment that minimized their ability to perform the work requirements, home management, social leisure, and relationships.</p><p><strong>Conclusions: </strong>The addiction to amphetamines was associated with high impairment of work performance and social obligations and a negative impact on the addict's mental health. The risk of suffering anxiety, depression, and bipolar is higher than in nonaddict people. These effects are attributed to brain damage, neurotoxicity, and neuronal inflammation, particularly when these substances are abused over extended periods and at higher doses.</p>","PeriodicalId":17421,"journal":{"name":"Journal of Toxicology","volume":"2024 ","pages":"1643693"},"PeriodicalIF":3.4,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11321892/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141976018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}