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This one would seem to support strongly the conclusion that the

distribution/form/mechanics of even *acute* Bb infections are very

different in humans than in gerbils.

THat would obviously be of high importance.

However - look at the doses used to cure the gerbils - waaaay

higher /kg than those used on the humans. This is not the first time

Ive seen what looks like huge doses, on a per kilogram basis, tested

on rodents. (I'm talking about infection clearance studies, not

toxicity studies, which of course involve immense doses for

understandable reasons.) Does anyone know why people give 25 mg/kg of

roxy to an experimentally infected gerbil when no human is going to

be taking that much? Are rodents somehow metabolizing all abx way way

faster than we are, or for some other reason need a huge dose to get

the same serum concentrations we get?

===================================================

Acta Derm Venereol. 1992 Aug;72(4):297-300.

Roxithromycin in Lyme borreliosis: discrepant results of an in vitro

and in vivo animal susceptibility study and a clinical trial in

patients with erythema migrans.

Hansen K, Hovmark A, Lebech AM, Lebech K, Olsson I, Halkier-Sorensen

L, Olsson E, Asbrink E.

Department of Infection-Immunology, Statens Seruminstitut,

Copenhagen, Denmark.

A new semisynthetic macrolide roxithromycin was evaluated for its

potential use in the treatment of Lyme borreliosis. Using a macro-

dilution broth technique, Borrelia burgdorferi was shown to be

susceptible to roxithromycin with a minimal bactericidal

concentration (MBC) of 0.06-0.25 microgram/ml. A systemic B.

burgdorferi infection was established in gerbils; a dosage of greater

than or equal to 25 mg/kg/day roxithromycin for 10 days eliminated

the infection. A single blind, randomized multicenter study was

performed to evaluate the efficacy of roxithromycin 150 mg b.i.d.

versus phenoxymethyl-penicillin 1 g b.i.d. for 10 days in patients

with uncomplicated erythema migrans. The study was interrupted when

19 patients had enrolled because of five treatment failures. All 5

patients had received roxithromycin; three patients had persisting or

recurrent erythema migrans, one developed a secondary erythema

migrans-like lesion and severe arthralgia and one developed

neuroborreliosis. B. burgdorferi was isolated from skin biopsies

after roxithromycin therapy from two patients with persistent

erythema migrans and both isolates were still highly susceptible to

roxithromycin (MBC = 0.03 microgram/ml). No treatment failures were

seen in 10 patients treated with phenoxymethyl-penicillin.

Roxithromycin is thus not recommended for treatment of Lyme

borreliosis.

Publication Types:

Clinical Trial

Multicenter Study

Randomized Controlled Trial

PMID: 1357894 [PubMed - indexed for MEDLINE]

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I found that the dosing levels used by doctor's in pill antibiotics

ain't cutting it. Healthy people seem to attack the same infection

constantly in antibiotic waves for years on end.(close relative)Many

of my observations of anyone tackling infection seem not to get the

job done.I find that the immune system possably covers the doctor 9

times out of 10- wherever this is possable.We fall out because our

immune system doesn't exist in the quagmire of our blood.

> This one would seem to support strongly the conclusion that the

> distribution/form/mechanics of even *acute* Bb infections are very

> different in humans than in gerbils.

>

> THat would obviously be of high importance.

>

> However - look at the doses used to cure the gerbils - waaaay

> higher /kg than those used on the humans. This is not the first

time

> Ive seen what looks like huge doses, on a per kilogram basis,

tested

> on rodents. (I'm talking about infection clearance studies, not

> toxicity studies, which of course involve immense doses for

> understandable reasons.) Does anyone know why people give 25 mg/kg

of

> roxy to an experimentally infected gerbil when no human is going

to

> be taking that much? Are rodents somehow metabolizing all abx way

way

> faster than we are, or for some other reason need a huge dose to

get

> the same serum concentrations we get?

>

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

>

> Acta Derm Venereol. 1992 Aug;72(4):297-300.

>

> Roxithromycin in Lyme borreliosis: discrepant results of an in

vitro

> and in vivo animal susceptibility study and a clinical trial in

> patients with erythema migrans.

>

> Hansen K, Hovmark A, Lebech AM, Lebech K, Olsson I, Halkier-

Sorensen

> L, Olsson E, Asbrink E.

>

> Department of Infection-Immunology, Statens Seruminstitut,

> Copenhagen, Denmark.

>

> A new semisynthetic macrolide roxithromycin was evaluated for its

> potential use in the treatment of Lyme borreliosis. Using a macro-

> dilution broth technique, Borrelia burgdorferi was shown to be

> susceptible to roxithromycin with a minimal bactericidal

> concentration (MBC) of 0.06-0.25 microgram/ml. A systemic B.

> burgdorferi infection was established in gerbils; a dosage of

greater

> than or equal to 25 mg/kg/day roxithromycin for 10 days eliminated

> the infection. A single blind, randomized multicenter study was

> performed to evaluate the efficacy of roxithromycin 150 mg b.i.d.

> versus phenoxymethyl-penicillin 1 g b.i.d. for 10 days in patients

> with uncomplicated erythema migrans. The study was interrupted

when

> 19 patients had enrolled because of five treatment failures. All 5

> patients had received roxithromycin; three patients had persisting

or

> recurrent erythema migrans, one developed a secondary erythema

> migrans-like lesion and severe arthralgia and one developed

> neuroborreliosis. B. burgdorferi was isolated from skin biopsies

> after roxithromycin therapy from two patients with persistent

> erythema migrans and both isolates were still highly susceptible

to

> roxithromycin (MBC = 0.03 microgram/ml). No treatment failures

were

> seen in 10 patients treated with phenoxymethyl-penicillin.

> Roxithromycin is thus not recommended for treatment of Lyme

> borreliosis.

>

> Publication Types:

> Clinical Trial

> Multicenter Study

> Randomized Controlled Trial

>

> PMID: 1357894 [PubMed - indexed for MEDLINE]

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,

Yes, I remarked on this when I was trying to work out dosages for something or other and I was told that rodents did require higher doses per weight. Too lazy to check it out but that was defintely the answer I got

Look at the full-text version of "the hamster study" that Jill and I are closely looking at at the moment re Babesia treatment and tell me what you think of the doses used, they seem HUGE (for not very good results, in fact, eradication of babesias being measured by surpassaging into healthy hamsters)

http://aac.asm.org/cgi/reprint/41/1/91.pdf

Nelly

[infections] assorted

This one would seem to support strongly the conclusion that the distribution/form/mechanics of even *acute* Bb infections are very different in humans than in gerbils.THat would obviously be of high importance.

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