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Thanks Ian.

Good for David Bruns.

My interest is in the possible ex vivo generation of D-lactate, in the
presence of fluoride. It could be generated from methylglyoxal (see
Annals 2010;47, page 269) itself potentially derived from the action
of triose phosphate isomerase, during normal glycolytic metabolism.

But if fluoride is a rapid inhibitor of enolase, that is not going to happen.

Nick

On 24 June 2010 14:19, ianholbrook <[log in to unmask]> wrote:
> Nick
> See
> Clinical Chemistry 54: 930-932, 2008
>
> http://www.clinchem.org/cgi/content/full/54/5/930
>
>
> Kind regards
> Ian
> -----Original Message-----
> From: Clinical biochemistry discussion list
> [mailto:[log in to unmask]] On Behalf Of Nick Miller
> Sent: 24 June 2010 14:09
> To: [log in to unmask]
> Subject: Re: FW: CSF analysis
>
> I know this is a widely held view, but can anyone prove to me that fluoride
> (by which we mean 5.0 mg of sodium fluoride in a maximum of 2.0 ml of
> sample) "stops lactate production immediately"? (see below)
>
> Nick Miller
> London
>
> On 24 June 2010 11:08, Holbrook, Ian B <[log in to unmask]> wrote:
>>
>> ________________________________
>> From: Holbrook, Ian B
>> Sent: 24 June 2010 11:07
>> To: 'Turner Helen (NHS Grampian)'
>> Cc: 'Dina'
>> Subject: RE: CSF analysis
>>
>> Dear Helen
>>
>> On behalf of the UK Specialist Advisory Group for EQA of CSF Proteins
>> and Biochemistry we would ALWAYS recommend analysing CSF if sufficient
>> sample is received. This is precious material that often cannot be
> repeated.
>>
>> If a blood stained CSF sample has a protein level within the reference
>> range then this is useful information to the clinician. If it is above
>> the reference range then of course appropriate comments must be added
>> to help in interpretation. If the results could have been affected by
>> the state of the CSF, delays in transport, not protected from the
>> light etc. then comments on interpretation will form part of the report.
>>
>> I would think that you could analyse CSF glucose in an unpreserved
>> sample as long as this was done within an hour of collection. Fluoride
>> stops lactate production immediately but does not stop glucose
>> utilisation for an hour or so. There would probably be little
>> difference, therefore, between preserved and unpreserved samples within an
> hour of collection.
>>
>> Kind regards
>>
>> Ian
>>
>>
>> Ian Holbrook
>>
>> Department of Clinical Biochemistry
>>
>> York Hospital
>>
>> Wigginton Road
>>
>> York
>>
>> YO31 8HE
>>
>> 01904 725786
>>
>>
>>
>> ________________________________
>> From: Clinical biochemistry discussion list
>> [mailto:[log in to unmask]] On Behalf Of Turner Helen
>> (NHS
>> Grampian)
>> Sent: 22 June 2010 17:52
>> To: [log in to unmask]
>> Subject: CSF analysis
>>
>> Dear readers,
>>
>> We are currently having a few disagreements regarding CSF analysis and
>> hence I'm looking for some advice.
>>
>> 1- How to deal with blood stained samples for CSF protein, glucose,
>> IgG, albumin and oligoclonal band analysis. Should these be reported
>> as unsuitable, or analysed with a comment to say interpret with
>> caution due to blood stained sample? In the case of oligoclonal bands-
>> does the fact the sample is blood stained have an effect?
>>
>> 2- Tube type for CSF Glucose analysis. Does this have to be a Fl-Ox
>> tube, or can a plain universal be used if received in the lab quickly
> (<1hr).
>>
>>
>> Thanks in advance
>>
>> Helen
>>
>> Clinical Biochemist
>> Department of Clinical Biochemistry
>> 1st Floor Link Building
>> Aberdeen Royal Infirmary
>> Foresterhill
>> Aberdeen
>> AB25 2ZD
>>
>> Tel: 01224 552831
>>
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