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mineral iron is very reactive and not suitable as a mineral

supplement.

it is typical of corp stupidity that it added to cereals

if a fraction of the marketing buget was spent on researching thier

additives!!!!!!!!!!!!!!!

but people work thier packaged lives and eat packages and the box

comes unwound....

> http://www.cfsan.fda.gov/~rdb/opa-g042.html I read the thing I

still

> don't know what it will do for anyone? ltldab1@ juno.com

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  • 6 months later...

I think lactoferrin also has the ability to help the gut get rid of

excess iron, which bacteria thrive on/in. So it has that bonus, as

well as immune system bonuses as well. I use colostrum with both my

kids.

W

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Tina,

You need cysteine inside cells to help produce your own lactoferrin, as

mentioned below, especially if you want to have success against candida.

This makes sense because iron binding sites, such as you have in

lactoferrin, need to have sulfur to maintain their iron binding capability.

The availability of cysteine to cells is furnished through such molecules

as cystine, glutathione and mixed disulfides, but if these are having a

hard time getting into cells, or being processed inside cells, then

intracellular (intra-Golgi) cysteine can be low even if plasma cysteinyl

groups are high. So it might be appropriate to enhance this side of the

chemistry in someone having intracellular sulfur supply problems.

Curiously, both casein and lactoferrin help to preserve the activity of

IGF-1, which is a growth factor that is very critical to postnatal brain

development and is very tied up with sulfation issues that are going on in

the brain postnatally. For that reason, it makes sense that breastmilk

includes both casein and lactoferrin since infancy is such an intensive

time for the myelination and sulfation of the brain. ...a process that

continues through toddlerhood, and in some areas till young

adulthood. This process is likely to be delayed in children with

developmental delays. But because casein is problematic for other reasons,

the lactoferrin might be an alternative way to help preserve the IGF-1

activity. Also, in those with a leaky gut, the leakiness is likely to have

been caused by poor sulfation of the gut by molecules such as mucins and

glycosaminoglycans. The article below suggests that the glycosaminoglycan

heparin in the stomach also helps to preserve IGF-1. That heparin might be

undersulfated if the supply of cysteine deep inside the cells is

wanting. That could be another reason lactoferrin might furnish a needed

boost to sulfation.

Kansenshogaku Zasshi 1998 Jul;72(7):727-37 Related Articles, Links

[Reverting effect of cysteine on the suppression by glucose or

dexamethasone of anti-Candida activity of human neutrophils]

[Article in Japanese]

Tansho T.

Department of Surgery II, Teikyo University School of Medicine.

Amino acid mixture prescribed for an hyperalimentation solution

(PN-twin) diminishes suppression of anti-Candida activity of neutrophils as

reported previously (Tansho, T, et al. J. Jpn. Assoc. Infect. Dis. 70:

463-469). The aim of this study was to identify the active principle in the

amino acid mixture and to examine its action mechanism. Amino acid mixture

(PN-twin) containing 23 amino acids neutralized the suppression of

anti-Candida activity of human neutrophils by 1.0% of glucose. These amino

acids were divided to several groups by their structure and effects of the

groups on the suppressed anti-Candida activity neutrophils were examined.

In all groups tested, amino acids containing cystein and methionine clearly

neutralized the suppression, especially cysteine at the concentration more

than 20 micrograms/ml significantly recovered the anti-Candida activity of

neutrophils which was suppressed in the presence of 1% glucose or 10(-6) M

dexamethasone. Correspondingly, cysteine augmented production of

lactoferrin by stimulated neutrophils; which functions as a major effector

molecule in growth inhibition of Candida by neutrophils. These results

suggest that cysteine in alimentation solution augments anti-Candida

defense mechanisms through recovery of neutrophil function.

PMID: 9745223 [PubMed - indexed for MEDLINE]

Degradation of IGF-I in the adult rat gastrointestinal tract is limited by a

specific antiserum or the dietary protein casein.

Xian CJ, Shoubridge CA, Read LC

ative Research Centre for Tissue Growth and Repair, Women's and

Children's Hospital, North Adelaide, Australia.

To investigate the potential of IGF-I peptides as therapeutics in the gut,

the survival profiles of a bolus of 125I-labelled IGF-I

(8.6 ng) in vivo in various ligated gut segments of fasted adult rats have

been examined. The intactness of IGF-I tracer in the

flushed luminal contents was estimated by trichloroacetic acid

precipitation, antibody and receptor binding assays. It was found

that IGF-I was degraded very rapidly in duodenum and ileum segments with a

half-life (t1/2) of 2 min by all three methods.

IGF-I was slightly more stable in the stomach (t1/2 = 8, 5 and 2.5 min by

the above three methods), and considerably more

stable in the colon (t1/2 = 38, 33 and 16 min as judged by the three

methods). Rates of degradation in gut flushings in vitro

were similar to the in vivo rates except for the colon, where IGF-I was

proteolysed more rapidly in vivo. As a means of

developing gut-stable and active forms of IGF-I, several approaches were

examined for their effectiveness in prolonging IGF-I

survival in the upper gut. It was found that the extension peptide on the

analogue, LR3IGF-I did not protect IGF-I, nor did

association with IGF-binding protein-3. However, an IGF-I antiserum was

effective in prolonging IGF-I half-life in duodenum

fluid by 28-fold. Charge interaction between IGF-I and heparin could also

protect IGF-I in the stomach but not in duodenum

flushings. Furthermore, casein (a non-specific dietary protein) and to a

lesser extent, BSA and lactoferrin, were effective in

preserving IGF-I structural integrity and receptor binding activity in both

stomach and duodenum fluids. It can be concluded

that IGF-I cannot be expected to retain bioactivity if delivered orally

because of rapid proteolysis in the upper gut, but the use

of IGF antibodies and casein could represent useful approaches for IGF-I

protection in oral formulae.

PMID: 7561632, UI: 96030699

At 02:25 PM 12/31/2002 +0000, you wrote:

>We have been on the GFCF diet for about 1.5 years without any major

>dramatic changes. We will be chelating after we get our test results

>back, but I was wondering about lactoferrin, the protective immune

>property found in human milk. I read another post in which the

>parent talked about the dramatic changes her child experienced after

>giving him lactoferrin. She had done the diet and anti-fungals with

>no result until she added lactoferrin. She said it was easier to rid

>his body of metals after that too. If anyone has any experience or

>information on this I would greatly appreciate it.

>

>Thanks,

>

>Tina

>

>

>=======================================================

>

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