Aminosulfonic Acid Research Articles

Stearidonic acid improves eicosapentaenoic acid status: studies in humans and cultured hepatocytes.

Ahiflower oil from the seeds of Buglossoides arvensis is rich in α-linolenic acid (ALA) and stearidonic acid (SDA). ALA and SDA are potential precursor fatty acids for the endogenous synthesis of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which are n3-long chain polyunsaturated fatty acids (n3-LC-PUFAS), in humans. Since taurine, an amino sulfonic acid, is often associated with tissues rich in n3-LC-PUFAS (e.g., in fatty fish, human retina), taurine may play a role in EPA- and DHA-metabolism. To examine the capacity of the plant-derived precursor fatty acids (ALA and SDA) and of the potential fatty acid metabolism modulator taurine to increase n3-LC-PUFAS and their respective oxylipins in human plasma and cultivated hepatocytes (HepG2 cells). In a monocentric, randomized crossover study 29 healthy male volunteers received three sequential interventions, namely ahiflower oil (9 g/day), taurine (1.5 g/day) and ahiflower oil (9 g/day) + taurine (1.5 g/day) for 20 days. In addition, cultivated HepG2 cells were treated with isolated fatty acids ALA, SDA, EPA, DHA as well as taurine alone or together with SDA. Oral ahiflower oil intake significantly improved plasma EPA levels (0.2 vs. 0.6% of total fatty acid methyl esters (FAMES)) in humans, whereas DHA levels were unaffected by treatments. EPA-levels in SDA-treated HepG2 cells were 65% higher (5.1 vs. 3.0% of total FAMES) than those in ALA-treated cells. Taurine did not affect fatty acid profiles in human plasma in vivo or in HepG2 cells in vitro. SDA-rich ahiflower oil and isolated SDA led to an increase in EPA-derived oxylipins in humans and in HepG2 cells, respectively. The consumption of ahiflower oil improves the circulating levels of EPA and EPA-derived oxylipins in humans. In cultivated hepatocytes, EPA and EPA-derived oxylipins are more effectively increased by SDA than ALA.

Physiological role of genes involved in taurine biosynthesis in fishes and in silico approach to determine transcription factors in their promoters’ zone

Taurine, an amino sulfonic acid that is sometimes referred to as an amino acid, is endogenously synthesized by the action of the key genes/enzymes: cysteine dioxygenase (cdo), cysteine sulfonate decarboxylase (csad), glutamate decarboxylase (gad), and 2-amino ethanethiol dioxygenase (ado). The taurine transporter (taut) also distributes this taurine formation across the plasma. These genes have been identified as important in different physiological processes such as reproduction, digestion, olfactory, visual, circulatory, and muscular systems. Thus, a literature review of these genes in fish has been described in the present work. Moreover, there is null information regarding the study of regulatory elements such as transcription factors (TFs) in taurine biosynthesis and transportation genes of fishes. In this interest and taking advantage of the availability of different sequence databases, bioinformatics can be applied as a first approach for an in silico identification of the putative TFs and transcription factor binding sites (TFBS) that might play an important role in regulating these genes. The results showed that some are commonly shared, whereas TFs and TFBs vary among fish species. Hence, binding sites for homeobox protein BarH-like 1 (BARX1), brain-specific homeobox protein homolog (BSX), helicase-like transcription factor (HLTF), homeobox protein Hox-A7 (HOXA7), homeobox protein Hox-B3 (HOXB3), homeobox protein Hox-B6 (HOXB6), homeobox protein Meis1 (MEIS1), homeobox protein Meis3 (MEIS3), nuclear factor of activated T cells 1 (NFATC1), and homeobox protein Nkx-6.2 (NKX6-2) were commonly found in the promoter regions of genes involved in taurine transportation and biosynthesis. Additionally, our results suggested that the frequency of HOXB3, a transcription factor involved in development, has repetitive TFBS sites in the promoter region of all species analyzed in the present study. Although bioinformatics gives us an approach to determine putative TFs and TFBS, further work is needed to verify how the found regulatory elements play a key role in taurine biosynthesis and transportation.

Acute taurine reduced alcohol intake and preference in alcohol-experienced, but not in alcohol-näive rats by central mechanisms

Taurine is a non-essential β sulfonated amino acid involved in a plethora of biological functions in the mammalian central nervous system. Taurine is easily accessible in energy drinks for human consumption. Previous preclinical and clinical reports suggest that acute systemic administration of taurine could inhibit some of the behavioral and metabolic effects of alcohol use disorder. Overall, both in rodent and human studies, acute taurine administration reduced voluntary alcohol intake. This study aimed to assess the pharmacological effects of taurine (intracerebroventricular; i.c.v.) on ethanol intake/preference of rats either control (i.e., alcohol naïve) or forced ethanol intake (since juvenile age with a chronic intermittent access model). In addition, to explore anxiety-like behavior (through defensive burying behavior test) as pharmacological control of taurine. We found that acute (i.c.v.) taurine reduced alcohol consumption, i.e., taurine significantly decreased both alcohol intake and preference in adult male Wistar rats. Moreover, taurine elicits an anxiolytic-like effect in all administered groups independently of previous alcohol exposure.

Inhibition of hydrogen evolution in proton battery by sulfamic acid-caprolactam electrolyte and its electrochemical study

Proton batteries are expected to be used in large-scale energy storage systems in the future because of their reliability, safety, non-toxicity, and low cost. However, the hydrogen evolution reaction in the electrolyte of a proton battery limits the development of a high-voltage proton battery, and it is difficult to study the anode materials with lower charge and discharge potential. In this study, a novel sulfamic acid-caprolactam based electrolytes for inhibiting hydrogen evolution in the proton batteries was investigated. Aminosulfonic acid was used as a proton source in the proton batteries for the first time. In addition, caprolactam cosolvent with double hydrogen bond site was added to the electrolyte to help H3O+ de-solvent into H+, which effectively inhibited the hydrogen evolution behavior in the electrolyte of proton battery. The MoO3 electrode showed good cycling stability in the SA-H2O-CPL electrolyte. After 300 cycles, the capacity retention rate was 83.3%, and the average CE value was 99.7%. After adding caprolactam to the electrolyte, the hydrogen evolution potential is reduced to -1.7 V, and the electrochemical stability window of the electrolyte is greatly widened, which will help to develop anode materials with lower redox potential and be of great significance to the realization of high voltage proton batteries.

Isolation and Structure Elucidation of Novel Mycosporine-like Amino Acids from the Two Intertidal Red Macroalgae Bostrychia scorpioides and Catenella caespitosa.

This study presents a phytochemical survey of two common intertidal red algal species, Bostrychia scorpioides and Catenella caespitosa, regarding their MAA (mycosporine-like amino acid) composition, which are known as biogenic sunscreen compounds. Six novel MAAs from Bostrychia scorpioides named bostrychines and two novel MAAs from Catenella caespitosa named catenellines were isolated using a protocol which included silica gel column chromatography, flash chromatography on reversed phase material and semipreparative HPLC (High-Performance Liquid Chromatography). The structure of the novel MAAs was elucidated using NMR (Nuclear Magnetic Resonance) and HR-MS (High-Resolution Mass Spectrometry), and their absolute configuration was confirmed by ECD (Electronic Circular Dichroism). All isolated MAAs possess a cyclohexenimine scaffold, and the metabolites from B. scorpioides are related to the known MAAs bostrychines A-F, which contain glutamine, glutamic acid and/or threonine in their side chains. The new MAAs from C. caespitosa contain taurine, an amino sulfonic acid that is also present in another MAA isolated from this species, namely, catenelline. Previous and new data confirm that intertidal red algae are chemically rich in MAAs, which explains their high tolerance against biologically harmful ultraviolet radiation.

An in-silico approach to the potential modulatory effect of taurine on sclerostin (SOST) and its probable role during osteoporosis

The cysteine-knot containing negative regulator of the Wnt (Wingless-related integration site) signaling pathway, sclerostin (SOST) is an emerging therapeutic target for osteoporosis. Its inhibition is responsible for the promotion of osteoblastogenesis. In this study, taurine, an amino sulfonic acid was used to study its mechanism of action for the inhibition of the SOST protein. Molecular docking and dynamic studies were performed as a part of the study whereby, it was observed that taurine binds to a probable allosteric pocket which allows it to modulate the structure of the SOST protein affecting all of the loops – loops 1, loop 2, and loop 3 – as well as the cysteine residues forming the cysteine-knot. The study also identified a set of seven taurine analogues that have better pharmacological activity than their parent compound using screening techniques. The conclusions derived from the study support that taurine has a probable antagonistic effect on the SOST protein directly through the modulation of HNQS motif and loops 2 and 3 and indirectly through its influence on the cysteine residues - 134, 165 and 167 C. Based on the results, it can be assumed that the binding of taurine with SOST protein probably reduces its binding affinity to the LRP6 protein greatly, while also inhibiting the target protein from anchoring to LRP4. Furthermore, it was noted that probable additional binding with any small molecule inhibitor (SMI) at the active site (PNAIG motif), in the presence of an already allosterically bound taurine, of the SOST protein would result in a complete potential antagonism of the target protein. Additionally, the study also uncovers the possible role of the GKWWRPS motif in providing stability to the PNAIG motif for the purpose of binding with LRP6. Communicated by Ramaswamy H. Sarma

Whole Body Distribution of Labile Coenzymes and Antioxidants in a Mouse Model as Visualized Using 1H NMR Spectroscopy.

Coenzyme A, acetyl coenzyme A, coenzymes of cellular energy, coenzymes of redox reactions, and antioxidants mediate biochemical reactions fundamental to the functioning of all living cells. There is an immense interest in measuring them routinely in biological specimens to gain insights into their roles in cellular functions and to help characterize the biological status. However, it is challenging to measure them ex vivo as they are sensitive to specimen harvesting, extraction, and measurement conditions. This challenge is largely underappreciated and carries the risk of grossly inaccurate measurements that lead to incorrect inferences. To date, several efforts have been focused on alleviating this challenge using NMR spectroscopy. However, a comprehensive solution for the measurement of the compounds in a wide variety of biological specimens is still lacking. As a part of addressing this challenge, we demonstrate here that the total pool of each group of unstable metabolites offers a starting place for the representation of labile metabolites in biological specimens. Based on this approach, in this proof-of-concept study, we determine the distribution of the labile compounds in different organs including heart, kidney, liver, brain, and skeletal muscle of a mouse model. The results were independently validated using different specimens and a different metabolite extraction protocol. Further, we show that both stable and unstable metabolites were distributed differentially in different organs, which signifies their differential functional roles, the knowledge of which is currently lacking for many metabolites. Intriguingly, the concentration of taurine, an amino sulfonic acid, in skeletal muscle is >30 mM, which is the highest for any metabolite in a mammalian tissue known to date. To the best of our knowledge, this is the first study to profile the whole body distribution of the labile and other high-concentration metabolites using NMR spectroscopy. The results may pave ways for gaining new insights into cellular functions in health and diseases.

Taurine: an essential amino sulfonic acid for retinal health.

Taurine: an essential amino sulfonic acid for retinal health.

Removal of the Harmful Nitrate Anions from Potable Water Using Different Methods and Materials, including Zero-Valent Iron.

Drinking water containing nitrate ions at a higher concentration level of more than 10 mg/L, according to the World Health Organization (WHO), poses a considerable peril to humans. This danger lies in its reduction of nitrite ions. These ions cause methemoglobinemia during the oxidation of hemoglobin into methemoglobin. Many protocols can be applied to the remediation of nitrate ions from hydra solutions such as Zn metal and amino sulfonic acid. Furthermore, the electrochemical process is a potent protocol that is useful for this purpose. Designing varying parameters, such as the type of cathodic electrode (Sn, Al, Fe, Cu), the type of electrolyte, and its concentration, temperature, pH, and current density, can give the best conditions to eliminate the nitrate as a pollutant. Moreover, the use of accessible, functional, and inexpensive adsorbents such as granular ferric hydroxide, modified zeolite, rice chaff, chitosan, perlite, red mud, and activated carbon are considered a possible approach for nitrate removal. Additionally, biological denitrification is considered one of the most promising methodologies attributable to its outstanding performance. Among these powerful methods and materials exist zero-valent iron (ZVI), which is used effectively in the deletion process of nitrate ions. Non-precious synthesis pathways are utilized to reduce the Fe2+ or Fe3+ ions by borohydride to obtain ZVI. The structural and morphological characteristics of ZVI are elucidated using UV–Vis spectroscopy, zeta potential, XRD, FE-SEM, and TEM. The adsorptive properties are estimated through batch experiments, which are achieved to control the feasibility of ZVI as an adsorbent under the effects of Fe0 dose, concentration of NO3− ions, and pH. The obtained literature findings recommend that ZVI is an appropriate applicant adsorbent for the remediation of nitrate ions.

Sulfamic acid is an environment-friendly alternative electrolyte for industrial acid cleaning and corrosion inhibition: a mini review

Abstract Sulfamic acid (H3NSO3), which is also known as amino sulfuric acid, sulfamidic acid, amidosulfonic acid, and aminosulfonic acid, is an industrially useful water-soluble colorless crystalline solid. Sulfamic acid solutions of different concentrations are widely used for the removal of scales and metal oxides deposits from the surface of metals and ceramics. Sulfamic acid solutions (5–10%) serve as alternative electrolytes for the removal of rusts and lime scales to replace relatively more irritating and volatile hydrochloric and sulfuric acid-based electrolytes. Sulfamic acid solutions can be regarded as relatively more environmentally friendly and less toxic electrolytes for the cleaning of metallic surfaces. However, similar to the popular acidic solutions, sulfamic acid based electrolytes are corrosive to metal and metallic structures. Therefore, organic compounds based corrosion inhibitors of natural and synthetic origin are widely used to prevent corrosive damage of metallic surfaces in such electrolytes. These compounds become effective by adsorbing on the metallic surface following through the Langmuir adsorption isotherm model. Using electrochemical analyses it was observed that organic corrosion inhibitors in sulfamic acid based electrolytes behave as mixed- and interface-type corrosion inhibitors and they become effective by adsorbing at the metal/electrolyte interfaces. The adsorption of most of the corrosion inhibitors mostly follows physiochemisorption mechanism.

Effects of Hydrostatic Pressure on Electrical Retinal Activity in a Multielectrode Array-Based ex vivo Glaucoma Acute Model.

Glaucoma is a heterogeneous eye disease causing atrophy of the optic nerve head (ONH). The optic nerve is formed by the axons of the retinal ganglion cells (RGCs) that transmit visual input to the brain. The progressive RGC loss during glaucoma leads to irreversible vision loss. An elevated intraocular pressure (IOP) is described as main risk factor in glaucoma. In this study, a multielectrode array (MEA)-based ex vivo glaucoma acute model was established and the effects of hydrostatic pressure (10, 30, 60, and 90 mmHg) on the functionality and survival of adult male and female wild-type mouse (C57BL/6) retinae were investigated. Spontaneous activity, response rate to electrical and light stimulation, and bursting behavior of RGCs was analyzed prior, during, and after pressure stress. No pressure related effects on spontaneous firing and on the response rate of the RGCs were observed. Even a high pressure level (90 mmHg for 2 h) did not disturb the RGC functionality. However, the cells’ bursting behavior significantly changed under 90 mmHg. The number of spikes in bursts doubled during pressure application and stayed on a high level after pressure stress. Addition of the amino sulfonic acid taurine (1 mM) showed a counteracting effect. OFF ganglion cells did not reveal an increase in bursts under pressure stress. Live/dead staining after pressure application showed no significant changes in RGC survival. The findings of our ex vivo model suggest that RGCs are tolerant toward high, short-time pressure stress.

The Disease-Modifying Role of Taurine and Its Therapeutic Potential in Coronavirus Disease 2019 (COVID-19).

Taurine is an amino sulfonic acid that is implicated in numerous physiological functions, including the regulation of oxidative stress, which plays an important role in coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), together with other pathophysiological processes. The recent finding of decreased serum taurine levels in SARS-CoV-2-infected patients, in tandem with its potential modulatory role in COVID-19 due to its antiviral, antioxidant, anti-inflammatory, and vascular-related effects, provides a rationale for considering taurine as a beneficial supplement in patients suffering from COVID-19. Here, we reviewed the potential disease-modifying effects of taurine and combined these with the current knowledge on COVID-19 to clarify the potential role of taurine in this respiratory disease.

Synthesis and characterization of amino sulfonic acid functionalized graphene oxide as a potential carrier for quercetin.

In this investigation, a new nanocomposite as a nanocarrier based on functionalized graphene oxide was synthesized by reaction of tetraethylenepentamine and chlorosulfonic acid with functional groups on the surface of GO. The synthesized nanocomposite was characterized by FT-IR, XRD TGA, FE-SEM, EDAX, TEM, and AFM analysis. To explore the potential of nanocomposites in drug delivery, the loading and releases of quercetin as an anticancer drug were investigated. The result displayed that more than 90% of the drug was loaded on the nanocarrier and the release of the drug is depending on the pH of the environment such that the releases of the drug in Gastric and intestinal conditions were up to 50% and 30%, respectively. The analysis of toxicity effect on the normal and cancer cells indicated that the nanocarrier with the drug has potential for cancer cells therapy without cytotoxic effect on normal cells in IC50 concentration.

Research on the Synthesis and Application of AminoSulfonic Acid Gemini Surfactant

Oil is a non-renewable resource, and it is essential to improve oil recovery. Surfactant flooding is a key technology in enhancing oil recovery. The present work aims to develop a new surfactant to the combination flooding system in oil displacement. The Aminosulfonic Acid Gemini Surfactant was prepared by using Hexadecylamine, 1-Butanaminium,N,N,N-tributyl-,bromide (1:1) and Sodium 2-chloroethyl sulfonate. The AminoSulfonic Acid Gemini Surfactant Sodium N,N’-Dihexadecyl-2-propanol- 1,3-ethylsulfonate SNNDPE) has better reaction temperature at 80℃. The best reaction time of SNNDPE is 12 h. Next, We made a characterization of SNNDPE. A new gemini surfactant was developed, which is beneficial to the research of material science. Then the performance of the new Gemini surfactant was tested. The surface tension tests suggested that the newly synthesized Aminosulfonic Acid Gemini Surfactant has higher surface activity. The resistance temperature of the Aminosulfonic Acid Gemini Surfactant solution is 80℃. Moreover, the oil-water interfacial tension experiment suggested that the minimum aqueous solution of the combination flooding system reaches an ultra-low level of 9.4 × 10−4 mN/m. The combination flooding system experiment results can be considered as a guidance in the design and studies of the combination flooding system for a selective.

Study of the composition and structure of ion-conducting membranes based on polyvinyl alcohol by 1H NMR spectroscopy

One of the alternative types of proton-conducting membranes for a hydrogen-air solid polymer fuel cell is the type of hybrid membranes based on polyvinyl alcohol (PVA) crosslinked with aldehyde, modified by sulfonic acid. Earlier, for the first time, we obtained new ion – conducting membranes based on furfural-crosslinked PVA modified aminosulfonic acid (ASA) and tetraethoxysilane (TEOS), as well as membranes not crosslinked with furfural (FUR) or unmodified ASA and TEOS, by a liquid-phase synthesis method, in an organic medium-dimethyl sulfoxide. The values of their ionic conductivity and the degree of swelling in water are presented. In this work, the composition and structure of the obtained ion-conducting membranes are studied using liquid-phase nuclear magnetic resonance (NMR) spectroscopy on 1H nuclei. In the 1H NMR spectrum of an ion – conducting membrane not cross-linked with the «PVA/ASA», the signal of free OH groups of PVA is observed to disappear, but at the same time a characteristic triplet at 7.1 ppm. is preserved, having a constant of ∼51 Hz and components of the same intensity (1:1:1), which corresponds to protons of 14NH4+ hydrolyzed ASA. The disappearance of the expanded signal at 9.6 m. d. of protons of the free sulfo group of ASA and a narrow singlet signal at 5.8 m. d. of free protons of the NH2 group of ASA indicates the interaction of ASA with OH groups of PVA. In the 1H NMR spectrum of an ion – conducting membrane crosslinked with FUR – «PVA/ASA/FUR», signals of protons of the furan ring of FUR and a signal of its aldehyde group are observed, which is shifted to a strong field, which is determined by the formation of a chemical bond between FUR and the polymer chain of PVA. In the 1H NMR spectra of all membranes modified by ASA, the appearance of a second weaker-field 14NH4+ triplet is observed, and in the spectra of a number of ion – conducting hybrid membranes modified by TEOS – «PVA/ASA/FUR/TEOS», signals of the third type of 14NH4+ triplets shifted in a strong field relative to the other two 14NH4+ triplets were detected. The appearance of additional 14NH4+ triplets indicates the formation of several bound forms of the ammonium ion.

Исследование состава и структуры ионопроводящих мембран на основе поливинилового спирта методом спектроскопии ЯМР 1 Н

One of the alternative types of proton-conducting membranes for a hydrogen-air solid polymer fuel cell is the type of hybrid membranes based on polyvinyl alcohol (PVA) crosslinked with aldehyde, modified with sulfonic acid. Earlier, for the first time, we obtained new ion – conducting membranes based on furfural-crosslinked PVA modified with amino sulfonic acid (ASA) and tetraethoxysilane (TEOS), as well as membranes not crosslinked with furfural (FUR) or unmodified ASA and TEOS, by a liquid-phase synthesis method, in an organic medium-dimethyl sulfoxide. The values of their ionic conductivity and the degree of swelling in water are presented. In this work, the composition and structure of the obtained ion-conducting membranes are studied using liquid-phase nuclear magnetic resonance (NMR) spectroscopy on 1 H nuclei. In the 1 H NMR spectrum of an ion – conducting membrane not cross-linked with the «PVA/ASA», the signal of free OH groups of PVA is observed to disappear, but at the same time a characteristic triplet at 7.1 m.d. is preserved, having a constant of ~51 Hz and components of the same intensity (1:1:1), which corresponds to protons of 14 NH 4 + hydrolyzed ASA. The disappearance of the expanded signal at 9.6 m. d. of protons of the free sulfo group of ASA and a narrow singlet signal at 5.8 m. d. of free protons of the NH 2 group of ASA indicates the interaction of ASA with OH groups of PVA. In the 1 H NMR spectrum of an ion – conducting membrane crosslinked with FUR – «PVA/ASA/FUR», signals of protons of the furan ring of FUR and a signal of its aldehyde group are observed, which is shifted to a strong field, which is determined by the formation of a chemical bond between FUR and the polymer chain of PVA. In the 1 H NMR spectra of all membranes modified by ASA, the appearance of a second weaker-field 14 NH 4 triplet is observed, and in the spectra of a number of ion – conducting hybrid membranes modified by TEOS – «PVA/ASA/FUR/TEOS», signals of the third type of 14 NH 4 + triplets shifted in a strong field relative to the other two 14 NH 4 + triplets were detected. The appearance of additional 14 NH 4 + triplets indicates the formation of several bound forms of the ammonium ion.

Electrochemical Behavior of Naphthalene 1-Nitro-6-Sulfonic Acid

Electrochemical behavior of naphthalene 1-nitro-6-sulfonic acid was studied by polarography, voltammetry on glassy carbon electrodes, and electrolysis at controlled potential and in galvanostatic mode. The 1-nitro-6-sulfonic acid, like α-nitronaphthalene and naphthalene 1-nitro-3,6,8-trisulphonic acid, was shown to be polarographically reduced in a strong acidic medium in the presence of 0.1 N H2SO4 to the corresponding naphthalene aminosulfonic acid in a single six-electron stage via an intermediate formation of hydroxylamine. Deceleration of the 1-nitro-6-sulfonic acid polarographic reduction manifesting itself as a decrease of the polarographic current, as well as strong dependence of the polarization curves’ parameters and shape on the neutral and alkaline supporting solution composition and pH, are related to anionic character of the species being reduced, which is caused by the presence of acidic sulfonic group in their molecules. The technological parameters for the naphthalene 1-amino-6-sulfonic acid preparative electrosynthesis are determined: the current density 5–10 A/dm2, temperature 30–32°C, and concentration of the initial nitro-compound 10–13%, which provide the target product yield of 87.0–93.5%, the current efficiency of 38.0–42.4%, and recovery of 69.0–80.0% (on the N3 grade nickel and Kh18N10Т-stainless-steel cathodes in ammonia buffer solutions with pH 7.0–8.2). To increase the electroreduction efficiency of the nitro-Cleve’s acids’ technical isomeric mixture reduction, the mixture preliminary purification and the using of inert atmosphere are recommended in the processes of both electrolysis and the target Cleve’s-acid extraction from the solution.

Does Taurine Preserve Visual Acuity in a Patient with Pathologic Myopia?

Taurine, a semi-essential amino sulfonic acid, is present in high amounts in the retina. It has anti-inflammatory, antioxidant, and neuromodulatory properties which have shown to be beneficial for specific neurodegenerative conditions [1]. However, its effects on high myopia or its complications are unknown. We report the case of a 60-year-old woman with pathological myopia, who 7 years ago, presented a best corrected visual acuity (BCVA) of 20/200 right eye (OD) and 20/70 left eye (OS), and was diagnosed with a choroidal neovascular membrane (CNV) OS. She initiated taurine supplementation (1.5 g/ daily for 14 days) and improved to a BCVA of 20/100 OD. She continued taking 500 mg/daily. Subsequent events included 4 injections of Aflibercept OS, cataract surgery in both eyes (AO), and peripheral retinal photocoagulation in AO. This last treatment induced a severe inflammation and loss of visual acuity OS. She was treated with corticosteroids, but after two weeks due to lack of improvement, the taurine dose was increased to 1 g/day. Three weeks after, her BCVA went from counting fingers to 20/60 OS, and her inflammation was controlled. After 7 years of continuous taurine intake, her CNV OS has remained inactive, her BCVA was stable and even improved in the last year from 20/45 OD and 20/80 OS to 20/25 OD and 20/60 OS, respectively. At the same time, her migraines decreased in intensity and frequency. This case report brings a new light towards the potential use of taurine supplementation in high myopia, retinal degeneration, and pathologic myopia.

Taurine Enhances Iron-Related Proteins and Reduces Lipid Peroxidation in Differentiated C2C12 Myotubes.

Taurine is a nonproteinogenic amino sulfonic acid in mammals. Interestingly, skeletal muscle is unable to synthesize taurine endogenously, and the processing of muscular taurine changes throughout ageing and under specific pathophysiological conditions, such as muscular dystrophy. Ageing and disease are also associated with altered iron metabolism, especially when there is an excess of labile iron. The present study addresses the question of whether taurine connects cytoprotective effects and redox homeostasis in a previously unknown iron-dependent manner. Using cultured differentiated C2C12 myotubes, the impact of taurine on markers of lipid peroxidation, redox-sensitive enzymes and iron-related proteins was studied. Significant increases in the heme protein myoglobin and the iron storage protein ferritin were observed in response to taurine treatment. Taurine supplementation reduced lipid peroxidation and BODIPY oxidation by ~60 and 25%, respectively. Furthermore, the mRNA levels of redox-sensitive heme oxygenase (Hmox1), catalase (Cat) and glutamate-cysteine ligase (Gclc) and the total cellular glutathione content were lower in taurine-supplemented cells than they were in the control cells. We suggest that taurine may inhibit the initiation and propagation of lipid peroxidation by lowering basal levels of cellular stress, perhaps through reduction of the cellular labile iron pool.

Comparative Metabolic Profiling of Two Contrasting Date Palm Genotypes Under Salinity

Since specific metabolites may be associated with salinity tolerance, this study aimed to decipher the salinity tolerance mechanism in date palm based on the information encoded by the metabolomic profiles of the salt-tolerant “Umsila” and salt-susceptible “Zabad” cultivars when grown under salinity conditions. Changes in the metabolomic profiles of the leaf and root tissues were determined using hydrophilic interaction liquid chromatography (HILIC) and reverse-phase liquid chromatography (RPLC) mass spectrometry. The global untargeted metabolomic analysis showed the presence of 4878 metabolites accumulated in leaf and root tissues of the date palm seedlings. Principal component analysis (PCA) revealed the presence of unique groups of metabolites for each treatment and tissue type. Pathway analysis showed the involvement of some of these metabolites in the biosynthesis of several types of membranous lipids and glycolipids molecules such as 18:0-lyso-phosphatidylethanolamine (lysoPE), and also the synthesis of cell-wall components such as 16-hydroxy hexadecanoic acid, which is an intermediate metabolite in cutin, suberin, and wax biosynthesis. Moreover, antioxidant flavonoids such as (+)-catechin and epicatechin, vitamins such as B9, phytohormone-associated compounds such as dihydrozeatin-9-N-glucoside-O-glucoside, and osmolytes such as the sulfonic amino acid taurine were all significantly (p ≤ 0.05, FWER ≤ 0.05) altered in response to salinity in both cultivars. These results indicate that salinity tolerance in date palm involved a multi-dimensional mechanism, which includes the modification of the cell-wall and cellular membranes, the production of oxygen species scavengers, the adjustment of cellular osmotic pressure, and probably the alteration of the hormonal balance. The intracultivar metabolomic profile comparison strategy performed in this study represents an approach that may pave the road toward the identification of salinity tolerance mechanisms in date palm based on the final protein products.