tisdag 18 juni 2019

Kissaeläimiltä puuttuu tauriinin synteesikoneista ja siksi ne syövät tauriininsa animaalilähteistä

Kissat  syövät  hiiriä  ehkä  tauriinin puutteen takia.

Leijonat, tiikerit ja muut kissaeläimet Felines,    ovat ihmiselle nälkäisinä  aina vaarallisa, koska ihminen on niille  essentiellin tauriinin lähde.  Niitten entsyymi cysteiinisulfiinihappodekarboksylaasi on vajeinen ja se on  tauriinin synteesiä  (rikkipitoisista aminohapoista metioniinista ja cysteiinistä käsin ) rajoittava entsyymi.  Metioniinin + cysteiinin saanti taas on ihmisellekin essentielliä - niitä tulee ravinnossa saada tietty määränsä, koska keho ei pysty  valmistamaan niitä, korkeintaan muokkaamaan valmiina saatuja  kehon interkonversioissa.


Metabolic bone disease in lion cubs at the London Zoo in 1889 - NCBI


av RW Chesney - ‎2010 - ‎Citerat av 14 - ‎Relaterade artiklar
24 aug. 2010 - Felines have limited amounts of cysteinesulfinic acid decarboxylase, a rate-limiting enzyme in the synthesis of taurine from methionine and cysteine, hence taurine is an essential amino acid in cats. ... Also, taurine is the most abundant free amino acid in goat milk [36].



Eri  tautitiloissa ihmisellä tauriinin synteesi on kompromittoitunutta ja liittyy moniin tauteihin.
Tässä onkin ajateltu jo kehittää tauriinianalogeja, jolloin ylitetään metaboliset esteet ja annetaan suoraan  tauriinia tai sen analogia lääkkeenomaisesti- kts. edellinen  artikkeli ja sitaattilähde.

Tauriinin ja beta-alaniinin kuljettaja SLC6A (3p25.1) , TAUT

https://www.ncbi.nlm.nih.gov/gene/6533
SLC6A  (3p25.1)
Official Symbol
SLC6A6provided by HGNC
Official Full Name
solute carrier family 6 member 6provided by HGNC
Also known as
TAUT
Summary
This gene encodes a multi-pass membrane protein that is a member of a family of sodium and chloride-ion dependent transporters. The encoded protein transports taurine and beta-alanine. There is a pseudogene for this gene on chromosome 21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]
Expression Ubiquitous expression in ovary (RPKM 26.5), spleen (RPKM 20.3) and 23 other tissues See more
Preferred Names
sodium- and chloride-dependent taurine transporter
Names
solute carrier family 6 (neurotransmitter transporter, taurine), member 6
 
Conserved Domains (1) summary
cd11510
Location:142683
SLC6sbd_TauT; Na(+)- and Cl(-)-dependent taurine transporter; solute-binding domain TauT is a Na(+)- and Cl(-)-dependent, high-affinity, low-capacity transporter of taurine and beta-alanine. Human TauT is encoded by the SLC6A6 gene. TauT is expressed in brain, retina, liver, kidney, heart, spleen, and pancreas. It may play a part in the supply of taurine to the intestinal epithelium and in the between-meal-capture of taurine. It may also participate in re-absorbing taurine that has been deconjugated from bile acids in the distal lumen. Functional TauT protects kidney cells from nephrotoxicity caused by the chemotherapeutic agent cisplatin; cisplatin down-regulates TauT in a p53-dependent manner. In mice, TauT has been shown to be important for the maintenance of skeletal muscle function and total exercise capacity. TauT-/- mice develop additional clinically important diseases, some of which are characterized by apoptosis, including vision loss, olfactory dysfunction, and chronic liver disease. This subgroup belongs to the solute carrier 6 (SLC6) transporter family.
ORIGIN      
        1 mgdaescllr qqtrevrkkp linyrflraa anaeprgpqa qrtscakrec gaftqrvrer
       61 agrqppaggt rhsraergrr rshprsrtrt tallrssqtk ematkeklqc lkdfhkdilk
      121 pspgkspgtr pedeaegkpp qrekwsskid fvlsvaggfv glgnvwrfpy lcykngggaf
      181 lipyfiflfg sglpvfflei iigqytsegg itcwekicpl fsgigyasvv ivsllnvyyi
      241 vilawatyyl fqsfqkelpw ahcnhswntp hcmedtmrkn ksvwitisst nftspviefw
      301 ernvlslspg idhpgslkwd lalclllvwl vcffciwkgv rstgkvvyft atfpfamllv
      361 llvrgltlpg agagikfyly pditrledpq vwidagtqif fsyaiclgam tslgsynkyk
      421 ynsyrdcmll gclnsgtsfv sgfaifsilg fmaqeqgvdi advaesgpgl afiaypkavt
      481 mmplptfwsi lffimllllg ldsqfveveg qitslvdlyp sflrkgyrre ifiafvcsis
      541 yllgltmvte ggmyvfqlfd yyaasgvcll wvaffecfvi awiyggdnly dgiedmigyr
      601 pgpwmkyswa vitpvlcvgc fifslvkyvp ltynktyvyp nwaiglgwsl alssmlcvpl
      661 vivirlcqte gpflvrvkyl ltprepnrwa veregatpyn srtvmngalv kpthiivetm
      721 m
//


Related articles in PubMed
GeneRIFs: Gene References Into Functions
  Katson vielä  yksityiskohtia "Features" tästä proteiinista: Siinä on jakso jossa on  näitöä prys- tyyppisiä ja myös  runsaasti w aminohappoa.
Natriumjonia  kiinnittää kohdat: 
(G157,V160,L499,D502..S503)
            ##Evidence-Data-END##
FEATURES             Location/Qualifiers
     source          1..721
                     /organism="Homo sapiens"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3p25.1"
     Protein         1..721
                     /product="sodium- and chloride-dependent taurine
                     transporter isoform c"
                     /note="sodium- and chloride-dependent taurine transporter;
                     solute carrier family 6 (neurotransmitter transporter,
                     taurine), member 6"
                     /calculated_mol_wt=81208
     Region          142..683
                     /region_name="SLC6sbd_TauT"
                     /note="Na(+)- and Cl(-)-dependent taurine transporter;
                     solute-binding domain; cd11510"
                     /db_xref="CDD:271398"
     Site            order(157,160,499,502..503)
                     /site_type="other"
                     /note="Na binding site 2 [ion binding]"
                     /db_xref="CDD:271398"
     Site            order(158..159,161..164,239,401..402,407,409,503,506..507)
                     /site_type="other"
                     /note="putative substrate binding site 1 [chemical
                     binding]"
                     /db_xref="CDD:271398"
     Site            order(159,164,402,434)
                     /site_type="other"
                     /note="Na binding site 1 [ion binding]"
                     /db_xref="CDD:271398"
     Site            order(166..167,238,242,245,468,472)
                     /site_type="other"
                     /note="putative substrate binding site 2 [chemical
                     binding]"
                     /db_xref="CDD:271398"
     Site            264
                     /site_type="other"
                     /note="putative glycosylation site [posttranslational
                     modification]"
                     /db_xref="CDD:271398"
     Site            280
                     /site_type="other"
                     /note="putative glycosylation site [posttranslational
                     modification]"
                     /db_xref="CDD:271398"
     Site            291
                     /site_type="other"
                     /note="putative glycosylation site [posttranslational
                     modification]"
                     /db_xref="CDD:271398"
     Site            634
                     /site_type="other"
                     /note="putative glycosylation site [posttranslational
                     modification]"
                     /db_xref="CDD:271398"
     CDS             1..721
                     /gene="SLC6A6"
                     /gene_synonym="TAUT"
                     /coded_by="NM_001134367.3:19..2184"
                     /note="isoform c is encoded by transcript variant 2"
                     /db_xref="CCDS:CCDS77704.1"
                     /db_xref="GeneID:6533"
                     /db_xref="HGNC:HGNC:11052"
                     /db_xref="MIM:186854"
 
 

uutta tietoa tauriinista

2019 Jun;24:101223. doi: 10.1016/j.redox.2019.101223. Epub 2019 May 21.
Taurine and its analogs in neurological disorders: Focus on therapeutic potential and molecular mechanisms. Jakaria M1, Azam S1, Haque ME1, Jo SH1, Uddin MS2, Kim IS3, Choi DK4.

Abstract

Taurine is a sulfur-containing amino acid and known as semi-essential in mammals and is produced chiefly by the liver and kidney. It presents in different organs, including retina, brain, heart and placenta and demonstrates extensive physiological activities within the body. In the several disease models, it attenuates inflammation- and oxidative stress-mediated injuries. Taurine also modulates ER stress, Ca2+ homeostasis and neuronal activity at the molecular level as part of its broader roles. Different cellular processes such as energy metabolism, gene expression, osmosis and quality control of protein are regulated by taurine.
 In addition, taurine displays potential ameliorating effects against different neurological disorders such as neurodegenerative diseases, stroke, epilepsy and diabetic neuropathy and protects against injuries and toxicities of the nervous system. Several findings demonstrate its therapeutic role against neurodevelopmental disorders, including Angelman syndrome, Fragile X syndrome, sleep-wake disorders, neural tube defects and attention-deficit hyperactivity disorder. Considering current biopharmaceutical limitations, developing novel delivery approaches and new derivatives and precursors of taurine may be an attractive option for treating neurological disorders. Herein, we present an overview on the therapeutic potential of taurine against neurological disorders and highlight clinical studies and its molecular mechanistic roles. This article also addresses the neuropharmacological potential of taurine analogs.

Tauriini munuaisen vajaatoiminnassa

https://www.ncbi.nlm.nih.gov/pubmed/29996172

2019 Feb;69(2):83-92. doi: 10.1055/a-0643-4604. Epub 2018 Jul 11.
Taurine Ameliorates Thyroid Hypofunction and Renal Injury in L-NAME-Induced Hypertensive Rats.

Abstract

There is a growing global interest in hypertension due to its associated complications including renal dysfunction in patients. The thyroid system reportedly regulates renal function in both animal and human. The present study investigated the therapeutic efficacy of taurine on renal and thyroid dysfunctions in hypertensive rats. Hypertension was induced by oral administration of nitric oxide synthase inhibitor, N-nitro L-arginine-methyl-ester (L-NAME), at 40 mg/kg body weight to the male Wistar rats for 14 consecutive days.
 The hypertensive rats were subsequently treated with either taurine (100 and 200 mg/kg) or reference drug atenolol (10 mg/kg) for another 14 consecutive days. Hypertensive rats showed renal damage evidenced by elevated plasma creatinine and urea levels when compared with normotensive control rats. Furthermore, L-NAME-induced hypertensive rats showed decreased circulatory concentrations of thyroid stimulating hormone, thyroxine, triiodothyronine and the ratio of triiodothyronine to thyroxine. The marked decrease in the renal antioxidant enzyme activities and nitric oxide level was accompanied by significant increase in myeloperoxidase activity and biomarkers of oxidative stress in hypertensive rats. Histological examination of kidneys from hypertensive rats revealed congestion of blood vessels, hemorrhagic lesion and disorganized glomerular structure. However, treatment with taurine or atenolol significantly reversed the suppression of thyroid function, ameliorated renal oxidative stress and histopathological lesions in L-NAME-induced hypertensive rats. Taurine may be a useful chemotherapeutic supplement in enhancing renal and thyroid functions in hypertensive patients.
PMID:
29996172
DOI:
10.1055/a-0643-4604
[Indexed for MEDLINE]

fredag 14 juni 2019

Metioniinista ja cysteiinistä . Hcy:n ja kystiinin asemista

Koska metioniinin osuus koskee niin selvästi  verenmuodostusta ja B12- vitamiini on tärkeä verelle, siitä on enemmän asiaa Veri ja hyytyminen blogista. Muta tämä Hcy.n transsulfuraatiotie (TS)  ja cysteiinin keskeinen osuus  vaatii kyllä cysteiiniasiat tähän  tauriiniblogiin, koska tauriini on jalo päätuote cysteiiniaineenvauhdunnasta. Hankaluuksia  rikkiaineenvaihdunnasas voi tulla  molekyylistä kystiini (cystatheine, cystat)  jossa on kaksi cysteiiniaminohappojohdannasta rikillä yhdistetty  yhdeksi isommaksi  molekyyliksi kaksiasteisessa transsulfuraatiossa  homocysteiinistä (Hcy) ja cysteiinistä (Cys)  käsin entsyymin avulla.  samalla mudostuu  H2S vetysulfidia, uutta  gasotramsmittoriainetta, joka on hyödyksi.  Tämä transsulfuraatiotie alkaa olla tarkan kartoituksen kohteena.uusia asioita löytyy muitakin kuin uusi kolmas gasotransmittori.   Cysteaminin muodostumisesta on uutta karttaa,  johon pitää tutustua.  Sitä voi muodostua kehossa ihmiselläkin.

Cysteiinin hajoaminen koe-eläimessä

http://www.biochemj.org/content/394/1/267Abstract
Mammalian metabolism of ingested cysteine is conducted principally within the liver. The liver tightly regulates its intracellular cysteine pool to keep levels high enough to meet the many catabolic and anabolic pathways for which cysteine is needed, but low enough to prevent toxicity. 

One of the enzymes the liver uses to regulate cysteine levels is CDO (cysteine dioxygenase). Catalysing the irreversible oxidation of cysteine, CDO protein is up-regulated in the liver in response to the dietary intake of cysteine

In the present study, we have evaluated the contribution of the ubiquitin–26 S proteasome pathway to the diet-induced changes in CDO half-life. 

 In the living rat, inhibition of the proteasome with PS1 (proteasome inhibitor 1) dramatically stabilized CDO in the liver under dietary conditions that normally favour its degradation. 
Ubiquitinated CDO intermediates were also seen to accumulate in the liver. Metabolic analyses showed that PS1 had a significant effect on sulphoxidation flux secondary to the stabilization of CDO but no significant effect on the intracellular cysteine pool. 

Finally, by a combination of in vitro hepatocyte culture and in vivo whole animal studies, we were able to attribute the changes in CDO stability specifically to cysteine rather than the metabolite 2-mercaptoethylamine (cysteamine).

 The present study represents the first demonstration of regulated ubiquitination and degradation of a protein in a living mammal, inhibition of which had dramatic effects on cysteine catabolism.

Abbreviations:
  CDO, cysteine dioxygenase;
 CSA, cysteine sulphinic acid;
 CSAD, CSA decarboxylase;
 CYS, cysteine;
HP, diet, high-protein diet;
 LP, diet, low-protein diet;
 MEA, 2-mercaptoethylamine or cysteamine;
OPA, o-phthalaldehyde;
PS1, proteasome inhibitor 1;
SBD-F, ammonium 4-fluoro-7-sulphobenzofurazan;
THF, tetrahydrofuran

CDO (5q22.3)  https://www.ncbi.nlm.nih.gov/gene/1036

Also known as  CDO-I
Expression  Biased expression in liver (RPKM 94.6), fat (RPKM 66.8) and 8 other tissues See more
Orthologs  mouse all
Preferred Names
cysteine dioxygenase type 1
Names
cysteine dioxygenase, type I
ORIGIN      
        1 meqtevlkpr tladlirilh qlfagdevnv eevqaimeay esdptewamy akfdqysrgr
       61 glqfvvgggs gggwlwytrn lvdqgngkfn lmilcwgegh gssihdhtns hcflkmlqgn
      121 lketlfawpd kksnemvkks ervlrenqca yindsiglhr venishtepa vslhlysppf
      181 dtchafdqrt ghknkvtmtf hskfgirtpn atsgslenn
//

Related articles in PubMed
 
2006 Jun;136(6 Suppl):1652S-1659S. doi: 10.1093/jn/136.6.1652S.
Mammalian cysteine metabolism: new insights into regulation of cysteine metabolism.
The mammalian liver tightly regulates its free cysteine pool, and intracellular cysteine in rat liver is maintained between 20 and 100 nmol/g even when sulfur amino acid intakes are deficient or excessive. By keeping cysteine levels within a narrow range and by regulating the synthesis of glutathione, which serves as a reservoir of cysteine, the liver addresses both the need to have adequate cysteine to support normal metabolism and the need to keep cysteine levels below the threshold of toxicity. Cysteine catabolism is tightly regulated via regulation of cysteine dioxygenase (CDO) levels in the liver, with the turnover of CDO protein being dramatically decreased when intracellular cysteine levels increase. This occurs in response to changes in the intracellular cysteine concentration via changes in the rate of CDO ubiquitination and degradation. Glutathione synthesis also increases when intracellular cysteine levels increase as a result of increased saturation of glutamate-cysteine ligase (GCL) with cysteine, and this contributes to removal of excess cysteine. When cysteine levels drop, GCL activity increases, and the increased capacity for glutathione synthesis facilitates conservation of cysteine in the form of glutathione (although the absolute rate of glutathione synthesis still decreases because of the lack of substrate). This increase in GCL activity is dependent on up-regulation of expression of both the catalytic and modifier subunits of GCL, resulting in an increase in total catalytic subunit plus an increase in the catalytic efficiency of the enzyme. An important role of cysteine utilization for coenzyme A synthesis in maintaining cellular cysteine levels in some tissues, and a possible connection between the necessity of controlling cellular cysteine levels to regulate the rate of hydrogen sulfide production, have been suggested by recent literature and are areas that deserve further study.
PMID:
16702335
DOI:
10.1093/jn/136.6.1652S

 The mammalian liver tightly regulates its intracellular free cysteine pool. In rats, for instance, intracellular cysteine is narrowly maintained between 20 and 100 nmol/g even when dietary protein or sulfur amino acid intake is varied from subrequirement to above-requirement levels for this species (1). The effect of diet on plasma and hepatic cysteine levels is illustrated by the data shown in Figure 1. Rats that had been adapted to a high-protein diet and then fed a low-protein diet supplemented with cysteine had, at 6 h after the diet was introduced, a large increase in the portal plasma cysteine concentration but no increase above the fasting value for cysteine in the arterial plasma or in the liver. On the other hand, the plasma cysteine concentration was not significantly decreased, compared with fasting levels, in rats fed a low-protein diet, whereas the hepatic cysteine concentration was markedly decreased. Thus, in rats, the liver allows its own cysteine concentration to vary about 5-fold (from 20 to 100 nmol/g) while regulating cysteine degradation to maintain the plasma cysteine concentration within a 2.5-fold range (between 80 and 200 μmol/L). By keeping cysteine levels within a very narrow range, the liver addresses 2 opposing homeostatic requirements. Cysteine levels must be sufficiently high to meet the needs of protein synthesis and the production of other essential molecules that include glutathione, coenzyme A, taurine, and inorganic sulfur. At the same time, however, cysteine concentrations must also be kept below the threshold of cytotoxicity. The potent toxicity of excess cysteine has been demonstrated in several animal models (24), and chronically high levels of cysteine have been closely associated with rheumatoid arthritis (5), Parkinson's disease (6), Alzheimer's disease (6), systemic lupus erythematosus (7), increased risk of cardiovascular disease (8), and adverse pregnancy outcomes in humans (9).

The central role of hepatic cysteine dioxygenase in regulation of cysteine levels.

An important enzyme that contributes to the regulation of steady-state intracellular cysteine levels is cysteine dioxygenase (CDO,4 EC 1.13.11.20). Expressed at high levels in the liver with lower levels in the kidney, brain, and lung, this iron metalloenzyme catalyzes the addition of molecular oxygen to the sulfhydryl group of cysteine, yielding cysteinesulfinic acid. The oxidative catabolism of cysteine to cysteinesulfinate by CDO represents an irreversible loss of cysteine from the free amino acid pool; cysteinesulfinate is shuttled into several pathways including hypotaurine/taurine synthesis, sulfite/sulfate production, and the generation of pyruvate; a metabolic flow chart in Figure 2 highlights CDO's position within the context of cysteine's catabolic pathways. In vivo data suggest that the liver, the organ with the highest amount of CDO protein expression and activity, may use CDO as a means of disposing of excess cysteine obtained through the diet and in the process conveniently generates cysteinesulfinate, the biosynthetic precursor of the essential metabolites sulfate, hypotaurine, and taurine (10). These final endproducts of cysteine sulfoxidation, from a toxicity standpoint, are far more benign than cysteine.
  A metabolic flow chart illustrating the position of CDO within the many pathways of cysteine metabolism. CDO catalyzes the first step in the major cysteine catabolic pathway and shunts cysteine toward the production of cysteinesulfinic acid, pyruvate, sulfate, hypotaurine, and taurine. For purposes of clarity, multistep pathways for cysteinesulfinate-independent routes of cysteine metabolism have been condensed to single arrows.

  ....

 

Utilization of cysteine for coenzyme A synthesis: new insights from the roles of pantothenate kinase and pantetheinase in the pathway.

Although the pathway for coenzyme A synthesis is well established, the rate of coenzyme A turnover and the extent of cysteine consumption for coenzyme A turnover have not been quantified. The flux-generating step in coenzyme A biosynthesis is the first step in the pathway and is catalyzed by pantothenate kinase. Cysteine is condensed with pantothenate in the second step of the coenzyme A synthesis pathway to form 4′-phosphopantothenoylcysteine, and the cysteine moiety is decarboxylated in the third step of the pathway to form the cysteamine, or β-mercaptoethylamine, moiety of coenzyme A. The rate of coenzyme A synthesis is determined largely by the regulated pantothenate kinase step, which is highly regulated in response to factors that favor lipid oxidation. Multiple isoforms of mammalian pantothenate kinase (PanK) are encoded by 4 genes in humans and in mice, and the regulatory properties of the various pantothenate kinase isoforms allow the robust control of coenzyme A biosynthesis by coenzyme A and its thioesters (39,40).
The human hereditary disorder pantothenate kinase-associated neurodegeneration (PKAN) has been associated with an accumulation of cysteine in the globus pallidus of the brain (41). Patients with PKAN show a pathological accumulation of iron in the basal ganglia and suffer from a gradual and steady deterioration of movement, speech, and cognition. The recent mapping of this disorder to mutations in the human PanK2 gene (42) suggested that impairment in coenzyme A synthesis could lead to cysteine accumulation in some tissues. Because PanK2 protein is widely expressed in tissues and is localized in the mitochondria, PKAN is thought to diminish mitochondrial function and adversely impact the globus pallidus and the retina, which are tissues with high metabolic requirements that are subject to oxidative damage. Iron accumulation in the brain is presumably caused by the lack of PanK2, which lowers the levels of 4′-phosphopantothenic acid and leads to the buildup of cysteine, which effectively binds iron. Cysteine is cytotoxic and, in the presence of iron, undergoes autooxidation, resulting in free radical formation. Free cysteine also enhances iron-induced lipid peroxidation. Thus, cysteine cytotoxicity as well as oxidative damage in the globus pallidus may contribute to the pathology of PKAN (42). From a metabolic point of view, the accumulation of cysteine suggests that its utilization for coenzyme A synthesis is important for regulation of its concentration in some tissues.
Even less is known about the regulation of coenzyme A degradation. Coenzyme A degradation involves sequential degradation of coenzyme A to dephospho-CoA + Pi, 4′-phosphopantetheine + AMP, and then pantetheine + Pi. In the final step of the degradation pathway, pantetheine is degraded to pantothenic acid and cysteamine (β-mercaptoethylamine) by an enzyme known as pantetheinase. Cysteamine can function as an antioxidant as well as a precursor for taurine biosynthesis. Little is known about the rate of cysteamine formation in mammalian tissues, but it is known that cysteamine can be converted to hypotaurine and, hence, to taurine.
Pitari et al. (43) recently reported that vanin-1–null mice were deficient in membrane-bound pantetheinase in liver and kidney and had negligible levels of cysteamine in their tissues. Vanin proteins were recently identified as pantetheinases on the basis of sequence similarity with pig pantetheinase (44). Vanin proteins are encoded by 2 genes in mice (vanin-1 and -3) and 3 in humans (vanin-1, -2, and -3) (4548). The unanticipated observation of pantetheinase deficiency in the vanin-1–null mouse model may facilitate efforts to evaluate the quantitative significance of coenzyme A turnover in vivo. If further work confirms a substantial rate of pantetheine formation and hydrolysis in mammalian tissues, this would imply a substantial rate of coenzyme A turnover, leading to a substantial pool of cysteamine for taurine biosynthesis. In this regard, we have observed higher plasma cysteamine concentrations in rats fed a high-protein (low-carbohydrate) diet (13 ± 2 μmol/L, mean ± SD) than in rats fed a low-protein (high-carbohydrate) diet (2.3 ± 0.7 μmol/L) and also in rats that had been fasted overnight (23 ± 4 μmol/L) compared with rats in an absorptive state (13 ± 2 μmol/L).

Pathways of taurine synthesis: cysteinesulfinate- and cysteamine-dependent pathways.

The pathways for taurine synthesis from cysteine are shown in Figure 7. The relative contribution of the cysteinesulfinate-dependent pathway versus the cysteamine-dependent pathway to net taurine production is not clear, largely because the magnitude of flux through the cysteamine pool has not been assessed. Several research groups, including our own laboratory, have focused their efforts on the cysteinesulfinate pathway, and we have shown that flux through this pathway is highly responsive to cysteine concentration (4953). Regulation of taurine biosynthesis via this pathway is mediated principally at the level of cysteine dioxygenase concentration, which is directly controlled by substrate concentration (17,18). Studies with isolated hepatocytes clearly show that changes in cysteine dioxygenase activity play a dominant role in determining the rates of both taurine and sulfate formation (5052).
FIGURE 7
Integration of cysteine and coenzyme A metabolic pathways involved in taurine synthesis. The key enzymes are (1) cysteine dioxygenase, (2) cysteinesulfinate decarboxylase, (3) pantothenate kinase, (4) dephospho-CoA kinase, (5) pantetheinase, and (6) cysteamine dioxygenase.
Integration of cysteine and coenzyme A metabolic pathways involved in taurine synthesis. The key enzymes are (1) cysteine dioxygenase, (2) cysteinesulfinate decarboxylase, (3) pantothenate kinase, (4) dephospho-CoA kinase, (5) pantetheinase, and (6) cysteamine dioxygenase.
When the cysteinesulfinate intermediate itself was used as substrate, the intact rat as well as isolated hepatocytes, renal cortical tubules, and enterocytes all exhibited a high capacity for cysteinesulfinate metabolism to CO2 or SO4, with rates of cysteinesulfinate oxidation far exceeding those for cysteine catabolism to CO2 or SO4 (5356). However, only hepatocytes had a high capacity for taurine synthesis from cysteinesulfinate, which is consistent with their higher level of cysteinesulfinate decarboxylase (CSD, EC 4.1.1.29) activity. This tissue difference in taurine production from cysteinesulfinate demonstrates that partitioning of cysteinesulfinate between decarboxylation and transamination pathways can potentially be regulated at the level of CSD activity. A modulatory role of CSD activity on partitioning of cysteinesulfinate to taurine has, in fact, been demonstrated in hepatocytes from rats fed high-protein or very high sulfur amino acid–containing diets. The amount of hepatic CSD decreased by up to 80% in rats fed a high-protein diet, and this was associated with a decreased rate of taurine production from cysteinesulfinate in studies done in vitro with hepatocytes from these rats (50). Despite the existence of regulation at the level of the partitioning of cysteinesulfinate between the decarboxylation (taurine) and transamination (pyruvate + sulfate) pathways, however, the overall flux of cysteine to taurine is largely driven by the dietary sulfur amino acid level and the associated changes in hepatic cysteine dioxygenase activity (i.e., by changes in rate of cysteinesulfinate production). Thus, despite a modest decrease in CSD activity in response to an increase in protein intake, the overall effect of an increase in protein intake is an increase in substrate for CSD and a large increase in taurine synthesis.
The high flux of cysteine through the cysteinesulfinate pathway under conditions of excess cysteine availability does not necessarily imply that the cysteamine pathway is a negligible contributor to taurine synthesis. On the contrary, there is ample indirect evidence for the synthesis of taurine via this route in the central nervous system and certain other tissues that express very low levels of cysteine dioxygenase and thus are unlikely to have substantial cysteine →taurine flux through the cysteinesulfinate pathway (57). Efforts to evaluate flux through the cysteamine pathway have been limited by incomplete data on the rate of coenzyme A turnover (58), by the technical difficulty in measuring cysteamine (59,60), and by the lack of definitive identification of cysteamine dioxygenase, the enzyme responsible for oxidation of cysteamine to hypotaurine (60).
We recently demonstrated that intact rats have a relatively large capacity for conversion of cysteamine to hypotaurine. Rats fed a basal low-protein diet (100 g casein/kg diet) supplemented with cysteamine or an equimolar amount of cysteine had markedly elevated levels of hypotaurine in liver, kidney, and brain at 6 and 10 h after introduction of the supplemented diet. As shown in Figure 8, tissue hypotaurine levels were higher in rats fed a diet supplemented with cysteine than in those fed a diet supplemented with an equimolar amount of cysteamine. This is consistent with cysteine being more readily converted to hypotaurine as a result of cysteine dioxygenase and cysteinesulfinate decarboxylase activities. Nevertheless, the increase (above basal, at 6 h) in hypotaurine level in liver and kidney of rats given supplemental cysteamine was 42 and 52% as much, respectively, as that observed in rats given an equimolar amount of supplemental cysteine, demonstrating that cysteamine is a good precursor of hypotaurine in vivo. This is even more striking because tissue cysteamine concentrations were not increased as much by cysteamine supplementation as cysteine concentrations were increased by cysteine supplementation. Supplementation of the diet with cysteine had no effect on tissue cysteamine concentrations, and supplementation of the diet with cysteamine had no effect on tissue cysteine concentrations. Thus, cysteamine can be converted to hypotaurine at a physiologically significant rate. Depending on the rate of cysteamine production via coenzyme A turnover, cysteamine could be a quantitatively important precursor of taurine.

Cystatiinista ja minne - cystiinistä vai cysteaminista tauriiniin

 https://www.ncbi.nlm.nih.gov/pubmed/30856117
2019;8(2):129-143. doi: 10.3233/JHD-180312.
Cysteamine Protects Neurons from Mutant Huntingtin Toxicity.
Arbez N1, Roby E1,2, Akimov S1, Eddings C1, Ren M1, Wang X1, Ross CA1,3.Abstract BACKGROUND:
The potential benefit of cysteamine for Huntington's disease has been demonstrated in HD animal models. Cysteamine and its derivate cystamine were shown to reduce neuropathology and prolong lifespan. Human studies have demonstrated safety, and suggestive results regarding efficacy. Despite all the studies available in vivo, there are only few in vitro studies, and the mechanism of action of cysteamine remains unclear. OBJECTIVE:
The objective of this study is to assess the capacity of cysteamine for neuroprotection against mutant Huntingtin in vitro using cellular models of HD, and to provide initial data regarding mechanism of action. METHODS:
We tested the neuroprotective properties of cysteamine in vitro in our primary neuron and iPSC models of HD. RESULTS:
Cysteamine showed a strong neuroprotective effect (EC50 = 7.1 nM) against mutant Htt-(aa-1-586 82Q) toxicity, in a nuclear condensation cell toxicity assay. Cysteamine also rescued mitochondrial changes induced by mutant Htt. Modulation of the levels of cysteine or glutathione failed to protect neurons, suggesting that cysteamine neuroprotection is not mediated through cysteine metabolism.
 Taurine and Hypotaurine, which are metabolites of cysteamine can protect neurons against Htt toxicity, but the inhibition of the enzyme converting cysteamine to hypotaurine does not block either protective activity, suggesting independent protective pathways.
 Cysteamine has been suggested to activate BDNF secretion;
however, cysteamine protection was not blocked by BDNF pathway antagonists.  CONCLUSIONS:
Cysteamine was strongly neuroprotective with relatively high potency. We demonstrated that the main neuroprotective pathways that have been proposed to be the mechanism of protection by cysteamine can all be blocked and still not prevent the neuroprotective effect. The results suggest the involvement of other yet-to-be-determined neuroprotective pathways. KEYWORDS:
Huntington’s disease; cysteamine; huntingtin toxicity; neurodegeneration; neuroprotection; patient-derived induced pluripotent stem cells; primary neurons



KYSTEAMINI (merkaptoetyyliamini)  on lääkemolekyyli, johdettu koentsyymi A:n degradaatiotiestä.  Se menee kehossa lysosomiin, jossa tekee yhdisteen kystiinin kanssa (Cystat)  ja tuottaa cysteiini(Cys)-cysteamini-disulfidin  ja cysteiiniä (Cys). Täten se saa cystiinipitoisuuden  alenemaan  ja sitä käytetään kystiinipitoisuuksien alentajana  kystinoosissa.

Cysteamin Svensk definition



Ett strålskyddsmedel som oxiderar i luft och bildar cystamin. Det ges intravenöst eller oralt mot strålsjuka. Bitartratet har använts för oral behandling av nefropatisk cystinos.

Bildresultat för cysteamine