Differential Diagnosis Disease Disorders 
Author Message
 Differential Diagnosis Disease Disorders

"Brain iron accumulation disorders, Huntington's disease , HDL1-3,
inherited prion disease, spinocerebellar ataxias 1, 3 and 17,
neuroacanthocytosis, dentatorubro-pallidoluysian atrophy (DRPLA),
Wilson's disease, benign hereditary chorea, Friedreich's ataxia ,
mitochondrial disease, vascular disease, post-infective autoimmune
central nervous system disorders (PANDAS), {*filter*}, systemic lupus
erythematosus, antiphospholipid syndrome, thyrotoxicosis, AIDS, chorea
gravidarum, and polycythaemia rubra vera. "

Pract Neurol. 2007 Nov;7(6):360-73.
The differential diagnosis of chorea.
Wild EJ, Tabrizi SJ.
Clinical Research Fellow and Honorary Clinical Assistant.

Chorea is a hyperkinetic movement disorder characterised by excessive
spontaneous movements that are irregularly timed, randomly distributed
and abrupt. In this article, the authors discuss the causes of chorea,
particularly Huntington's disease and the genetic syndromes that may
resemble it, including HDL1-3, inherited prion disease,
spinocerebellar ataxias 1, 3 and 17, neuroacanthocytosis, dentatorubro-
pallidoluysian atrophy (DRPLA), brain iron accumulation disorders,
Wilson's disease, benign hereditary chorea, Friedreich's ataxia and
mitochondrial disease. Acquired causes of chorea include vascular
disease, post-infective autoimmune central nervous system disorders
(PANDAS), {*filter*}, systemic lupus erythematosus, antiphospholipid
syndrome, thyrotoxicosis, AIDS, chorea gravidarum, and polycythaemia
rubra vera. The authors suggest an approach to the clinical assessment
of chorea, the value of investigations, including genetic tests (for
which they offer a structured framework highlighting the importance of
prior counselling), and finally briefly discuss symptomatic drug
treatment of chorea.

PMID: 18024776 [PubMed - in process]
---------------------------------------------------------------------------------

Trehalose opens new approach to treatment of polyglutamine diseases

Huntington's disease (HD) is a progressive neurodegenerative disorder
caused by a mutation that expands the CAG polyglutamine repeat in the
huntingtin gene beyond normal. As the formation of insoluble protein
aggregates may be linked to the cellular distortions underlying HD,
molecules or proteins that inhibit their formation have been
investigated at RIKEN. In vitro screening studies showed that various
disaccharides can inhibit polyglutamine-mediated protein aggregation.
The most potent compound, trehalose, stabilized proteins containing
an
expanded polyglutamine and decreased formation of aggregates dose-
dependently without inducing any cellular toxicity. {*filter*}
administration (2%) in the R6/2 transgenic mouse model of HD
decreased
polyglutamine aggregates in the cerebrum and liver, improved motor
dysfunction and extended life-span in a dose-dependent manner. The
elevated rate of diabetes in R6/2 mice mimics symptoms observed in HD
patients. The examination of fasting {*filter*} glucose in R6/2 and wild-
type trehalose-treated (2%) mice were comparable to that of control
mice. The interaction between disaccharide compounds and
polyglutamine-
mediated protein aggregation may provide a novel approach for the
treatment of polyglutamine diseases (Tanaka, M. et al. Nat Med 2004,
10(2): 148).

-------------------------------------------------------------------
http://www.***.com/

 It is particularly effective when combined with phosphate ions[2].
Trehalose has also been used in at least one biopharmaceutical
formulation, the monoclonal antibody trastuzumab, marketed as
Herceptin.
-------------------------------------------------------------------

http://www.***.com/

PROPERTIES OF TREHALOSETrehalose is a disaccharide composed of two
glucose molecules bound by an alpha, alpha-1, 1 linkage.Since the
reducing end of a glucosyl residue is connected with the other,
trehalose has no reducingpower. Trehalose is widely distributed in
nature. It is known to be one of the sources of energy in mostliving
organisms and can be found in many organisms, including bacteria,
fungi, insects, plants, andinvertebrates. Mushrooms contain up to 10-
25 % trehalose by dry weight. Furthermore, trehalose pro-tects
organisms against various stresses, such as dryness, freezing, and
osmopressure. In the case of res-urrection plants, which can live in
a
dry state, when the water dries up, the plants dry up too.
However,they can successfully revive when placed in water. The
anhydrobitic organisms are able to tolerate thelack of water owing to
their ability to synthesize large quantities of trehalose, and the
trehalose plays akey role in stabilizing membranes and other
macromolecular assemblies under extreme environmentalconditions.The
properties of trehalose are shown in Table 1. Its relative sweetness
is 45 % of sucrose.Trehalose has high thermostability and a wide pH-
stability range. Therefore, it is one of the most sta-ble
saccharides.
When 4 % trehalose solutions with 3.5 to 10 pH were heated at 100 C
for 24 h, nodegradation of trehalose was observed in any case.
Because
of nonreducing sugar, this saccharidedoes not show Maillard reaction
with amino compounds such as amino acids or proteins. Its partic-ular
physical features make it an extremely attractive substance for
industrial applications.Furthermore, this saccharide shows good
sweetness like sucrose, and in the cooking.net">food industry, this sac-charide is
used as a sweetener.*Pure Appl. Chem. Vol. 74, No. 7, 2002. A special
topic issue on the science of sweeteners.
---------------------------------------------------------------------------------

Who loves ya.
Tom

Jesus Was A Vegetarian!
http://www.***.com/

Man Is A Herbivore!
http://www.***.com/

DEAD PEOPLE WALKING
http://www.***.com/



Sun, 09 May 2010 23:34:13 GMT
 Differential Diagnosis Disease Disorders

Soooo .. this would be a brown rice mushroom .. medley .. sweetened
with .. honey .. ?

Phosphates from THE chaff / brown OF the rice .. trehalose from THE
mushroom and also trehalose from .. THE honey ..

Who loves ya.
Tom

Jesus Was A Vegetarian!
http://www.***.com/

Man Is A Herbivore!
http://www.***.com/

DEAD PEOPLE WALKING
http://www.***.com/

Quote:
> "Brain iron accumulation disorders, Huntington's disease , HDL1-3,
> inherited prion disease, spinocerebellar ataxias 1, 3 and 17,
> neuroacanthocytosis, dentatorubro-pallidoluysian atrophy (DRPLA),
> Wilson's disease, benign hereditary chorea, Friedreich's ataxia ,
> mitochondrial disease, vascular disease, post-infective autoimmune
> central nervous system disorders (PANDAS), {*filter*}, systemic lupus
> erythematosus, antiphospholipid syndrome, thyrotoxicosis, AIDS, chorea
> gravidarum, and polycythaemia rubra vera. "

> Pract Neurol. 2007 Nov;7(6):360-73.
> The differential diagnosis of chorea.
> Wild EJ, Tabrizi SJ.
> Clinical Research Fellow and Honorary Clinical Assistant.

> Chorea is a hyperkinetic movement disorder characterised by excessive
> spontaneous movements that are irregularly timed, randomly distributed
> and abrupt. In this article, the authors discuss the causes of chorea,
> particularly Huntington's disease and the genetic syndromes that may
> resemble it, including HDL1-3, inherited prion disease,
> spinocerebellar ataxias 1, 3 and 17, neuroacanthocytosis, dentatorubro-
> pallidoluysian atrophy (DRPLA), brain iron accumulation disorders,
> Wilson's disease, benign hereditary chorea, Friedreich's ataxia and
> mitochondrial disease. Acquired causes of chorea include vascular
> disease, post-infective autoimmune central nervous system disorders
> (PANDAS), {*filter*}, systemic lupus erythematosus, antiphospholipid
> syndrome, thyrotoxicosis, AIDS, chorea gravidarum, and polycythaemia
> rubra vera. The authors suggest an approach to the clinical assessment
> of chorea, the value of investigations, including genetic tests (for
> which they offer a structured framework highlighting the importance of
> prior counselling), and finally briefly discuss symptomatic drug
> treatment of chorea.

> PMID: 18024776 [PubMed - in process]
> ----------------------------------------------------------------------------------

> Trehalose opens new approach to treatment of polyglutamine diseases

> Huntington's disease (HD) is a progressive neurodegenerative disorder
> caused by a mutation that expands the CAG polyglutamine repeat in the
> huntingtin gene beyond normal. As the formation of insoluble protein
> aggregates may be linked to the cellular distortions underlying HD,
> molecules or proteins that inhibit their formation have been
> investigated at RIKEN. In vitro screening studies showed that various
> disaccharides can inhibit polyglutamine-mediated protein aggregation.
> The most potent compound, trehalose, stabilized proteins containing
> an
> expanded polyglutamine and decreased formation of aggregates dose-
> dependently without inducing any cellular toxicity. {*filter*}
> administration (2%) in the R6/2 transgenic mouse model of HD
> decreased
> polyglutamine aggregates in the cerebrum and liver, improved motor
> dysfunction and extended life-span in a dose-dependent manner. The
> elevated rate of diabetes in R6/2 mice mimics symptoms observed in HD
> patients. The examination of fasting {*filter*} glucose in R6/2 and wild-
> type trehalose-treated (2%) mice were comparable to that of control
> mice. The interaction between disaccharide compounds and
> polyglutamine-
> mediated protein aggregation may provide a novel approach for the
> treatment of polyglutamine diseases (Tanaka, M. et al. Nat Med 2004,
> 10(2): 148).

> ------------------------------------------------------------------- http://www.***.com/

>  [2].
> Trehalose has also been used in at least one biopharmaceutical
> formulation, the monoclonal antibody trastuzumab, marketed as
> Herceptin.
> -------------------------------------------------------------------

> http://www.***.com/

> PROPERTIES OF TREHALOSETrehalose is a disaccharide composed of two
> glucose molecules bound by an alpha, alpha-1, 1 linkage.Since the
> reducing end of a glucosyl residue is connected with the other,
> trehalose has no reducingpower. Trehalose is widely distributed in
> nature. It is known to be one of the sources of energy in mostliving
> organisms and can be found in many organisms, including bacteria,
> fungi, insects, plants, andinvertebrates. Mushrooms contain up to 10-
> 25 % trehalose by dry weight. Furthermore, trehalose pro-tects
> organisms against various stresses, such as dryness, freezing, and
> osmopressure. In the case of res-urrection plants, which can live in
> a
> dry state, when the water dries up, the plants dry up too.
> However,they can successfully revive when placed in water. The
> anhydrobitic organisms are able to tolerate thelack of water owing to
> their ability to synthesize large quantities of trehalose, and the
> trehalose plays akey role in stabilizing membranes and other
> macromolecular assemblies under extreme environmentalconditions.The
> properties of trehalose are shown in Table 1. Its relative sweetness
> is 45 % of sucrose.Trehalose has high thermostability and a wide pH-
> stability range. Therefore, it is one of the most sta-ble
> saccharides.
> When 4 % trehalose solutions with 3.5 to 10 pH were heated at 100 C
> for 24 h, nodegradation of trehalose was observed in any case.
> Because
> of nonreducing sugar, this saccharidedoes not show Maillard reaction
> with amino compounds such as amino acids or proteins. Its partic-ular
> physical features make it an extremely attractive substance for
> industrial applications.Furthermore, this saccharide shows good
> sweetness like sucrose, and in the cooking.net">food industry, this sac-charide is
> used as a sweetener.*Pure Appl. Chem. Vol. 74, No. 7, 2002. A special
> topic issue on the science of sweeteners.
> ----------------------------------------------------------------------------------

> Who loves ya.
> Tom

> Jesus Was A Vegetarian! http://www.***.com/

> Man Is A Herbivore! http://www.***.com/

> DEAD PEOPLE WALKING http://www.***.com/



Sun, 09 May 2010 23:48:11 GMT
 
 [ 2 post ] 

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