Guest guest Posted March 17, 2006 Report Share Posted March 17, 2006 The search lead[ti] AND (gastrointestinal[ti] OR intestin*[ti]) generated >100 citations. W/o the title-word restrictions, the search generates >6000 citations. Here are several from the first 20 of the >100. Several are free online by clicking the links that are presented so clearly when I send this email. *1: *J Appl Toxicol. <javascript:AL_get(this, 'jour', 'J Appl Toxicol.');> 2005 Sep-Oct;25(5):361-4. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Display & dopt=pubmed\ _pubmed & from_uid=16092086> Click here to read <http://www.ncbi.nlm.nih.gov/entrez/utils/lofref.fcgi?PrId=3058 & uid=16092086 & db=\ pubmed & url=http://dx.doi.org/10.1002/jat.1079> *Expression of brush border enzymes in response to lead exposure in rat intestine.* *Kapur P* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Kapur+P%22%5BAuthor%5D>, *Kaur K* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Kaur+K%22%5BAuthor%5D>, *Mahmood A* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Mahmood+A%22%5BAuthor%5D>. Department of Biochemistry, Panjab University, Chandigarh-160 014, India. The effect of feeding lead (50 mg kg(-1) body weight) daily for 7 days on the development of various brush border enzymes in the intestine has been studied. The activities of brush border sucrase (P < 0.001), lactase (P < 0.001), gamma-glutamyl transpeptidase (P < 0.05) and leucine aminopeptidase were reduced (P < 0.05), whereas the alkaline phosphatase level was augmented (P < 0.05) in lead fed rats compared with controls. Kinetic studies with sucrase revealed a low Vmax (0.224 in control and 0.160 units mg(-1) protein in lead exposed) with no change in Km (12.6-13.5 mM). Western blot analysis for alkaline phosphatase yielded intense staining of enzyme protein in lead fed rats compared with controls, however, the intensity of the antigen signal was reversed for sucrase under these conditions. These findings suggest that ingestion of lead may interfere with the crypt cell differentiation process thus affecting enzyme functions in the rat intestine. 2005 Wiley & Sons, Ltd. PMID: 16092086 [PubMed - indexed for MEDLINE] ------------------------------------------------------------------------ *2: *Environ Health Perspect. <javascript:AL_get(this, 'jour', 'Environ Health Perspect.');> 2005 Apr;113(4):491-3. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Display & dopt=pubmed\ _pubmed & from_uid=15811841> Click here to read <http://www.ncbi.nlm.nih.gov/entrez/utils/lofref.fcgi?PrId=3040 & uid=15811841 & db=\ pubmed & url=http://ehpnet1.niehs.nih.gov/members/2005/7594/7594.html> *Intoxication from an accidentally ingested lead shot retained in the gastrointestinal tract.* *Gustavsson P* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Gustavsson+P%22%5BAuthor%5D>, *Gerhardsson L* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Gerhardsson+L%22%5BAuthor%5D>. Department of Occupational and Environmental Health, Stockholm Centre for Public Health, Stockholm, Sweden. per.gustavsson@... A 45-year-old woman was referred to the Department of Occupational and Environmental Health in January 2002 because of increased blood lead concentrations of unknown origin. She suffered from malaise, fatigue, and diffuse gastrointestinal symptoms. She had a blood lead level of 550 microg/L (normal range < 40 microg/L). The patient had not been occupationally exposed to lead, and no potential lead sources, such as food products or lead-glazed pottery, could be identified. Her food habits were normal, but she did consume game occasionally. Clinical examination, including standard neurologic examination, was normal. No anemia was present. Laboratory tests showed an increased excretion of lead in the urine, but there were no signs of microproteinuria. An abdominal X ray in October 2002 revealed a 6-mm rounded metal object in the colon ascendens. Before the object could be further localized, the patient contracted winter vomiting disease (gastroenteritis) and the metal object was spontaneously released from the colon during a diarrhea attack. The object was a lead shot pellet, possibly but not normally used in Sweden for hunting wild boar or roe deer. Blood lead levels slowly decreased. Nine months later the patient's blood lead levels were almost normal (approximately 70 microg/L) and her symptoms had almost completely disappeared. In this case, a rare source of lead exposure was found. In investigations of blood lead elevations of unknown origin, we recommend abdominal X ray in parallel with repeated blood lead determinations. Publication Types: * Case Reports <javascript:AL_get(this, 'ptyp', 'Case Reports');> PMID: 15811841 [PubMed - indexed for MEDLINE] ------------------------------------------------------------------------ *3: *Rev Environ Health. <javascript:AL_get(this, 'jour', 'Rev Environ Health.');> 2003 Oct-Dec;18(4):231-50. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Display & dopt=pubmed\ _pubmed & from_uid=15025188> *Toxicity of environmental lead and the influence of intestinal absorption in children.* *Heath LM* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Heath+LM%22%5BAuthor%5D>, *Soole KL* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Soole+KL%22%5BAuthor%5D>, *McLaughlin ML* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22McLaughlin+ML%22%5BAuthor%5D>, *McEwan GT* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22McEwan+GT%22%5BAuthor%5D>, * JW* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22+JW%22%5BAuthor%5D>. Department of Environmental Health, School of Medicine, Flinders University, Adelaide, South Australia. Exposure to metals, particularly lead, remains a widespread issue that is associated with historical and current industrial practices. Whereas the toxic properties of metals are well described, exposure to metals per se is only one of many factors contributing to elevated blood metal concentrations and their consequent health effects in humans. The absorbed dose of metal is affected by geochemical, biochemical, and physiological parameters that influence the rate and extent of absorption. In children, the interplay among these factors can be of critical importance, especially when biochemical and physiological processes might not have matured to their normal adult status. Such immaturity represents an elevated risk to metal-exposed children because they might be more susceptible to enhanced absorption, especially via the oral route. This review brings together the more recent findings on the physiological mechanisms of metal absorption, especially lead, and examines several models that can be useful in assessing the potential for metal uptake in children. Publication Types: * Review <javascript:AL_get(this, 'ptyp', 'Review');> PMID: 15025188 [PubMed - indexed for MEDLINE] ------------------------------------------------------------------------ *4: *Arch Environ Contam Toxicol. <javascript:AL_get(this, 'jour', 'Arch Environ Contam Toxicol.');> 2003 Jan;44(1):116-24. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Display & dopt=pubmed\ _pubmed & from_uid=12434226> Click here to read <http://www.ncbi.nlm.nih.gov/entrez/utils/lofref.fcgi?PrId=3055 & uid=12434226 & db=\ pubmed & url=http://dx.doi.org/10.1007/s00-z> *In vitro intestinal lead uptake and transport in relation to speciation.* *Oomen AG* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Oomen+AG%22%5BAuthor%5D>, *Tolls J* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Tolls+J%22%5BAuthor%5D>, *Sips AJ* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Sips+AJ%22%5BAuthor%5D>, *Groten JP* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Groten+JP%22%5BAuthor%5D>. RITOX, Environmental Toxicology and Chemistry, Utrecht University, The Netherlands. agnes.oomen@... Children might be exposed substantially to contaminants such as lead via soil ingestion. In risk assessment of soil contaminants there is a need for information on oral bioavailability of soilborne lead. Oral bioavailability can be seen as the result of four steps: (1) soil ingestion; (2) mobilization from soil during digestion, i.e., bioaccessibility; (3) transport across the intestinal epithelium; and (4) first-pass effect. Lead bioaccessibility and speciation in artificial human small intestinal fluid, i.e., chyme, have been investigated in previous studies. In the present study, transport of bioaccessible lead across the intestinal epithelium was investigated using the Caco-2 cell line. Cell monolayers were exposed to (diluted) artificial chyme. In 24 h, approximately 27% of the lead were associated to the cells and 3% were transported across the cell monolayer, without signs of approaching equilibrium. Lead associated to the cells showed a linear relationship with the total amount of lead in the system. Bile levels did not affect the fraction of lead associated to Caco-2 cells. Extrapolation of the lead flux across the Caco-2 monolayer to the in vivo situation indicates that only a fraction of the bioaccessible lead is transported across the intestinal epithelium. Furthermore, the results indicate that as the free Pb(2+) concentration in chyme was negligible, lead species other than the free metal ion must have contributed to the lead flux toward the cells. On the basis of lead speciation in chyme, this can be attributed to dissociation of labile lead species, such as lead phosphate and lead bile complexes, and subsequent transport of the released free metal ions toward the intestinal membrane. PMID: 12434226 [PubMed - indexed for MEDLINE] ------------------------------------------------------------------------ *5: *Environ Health Perspect. <javascript:AL_get(this, 'jour', 'Environ Health Perspect.');> 2001 Jun;109(6):613-9. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Display & dopt=pubmed\ _pubmed & from_uid=11445516> Click here to read <http://www.ncbi.nlm.nih.gov/entrez/utils/lofref.fcgi?PrId=3040 & uid=11445516 & db=\ pubmed & url=http://ehpnet1.niehs.nih.gov/members/2001/109p613-619cremin/cremin-fu\ ll.html> *Oral succimer decreases the gastrointestinal absorption of lead in juvenile monkeys.* *Cremin JD Jr* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Cremin+JD+Jr%22%5BAuthor%5D>, *Luck ML* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Luck+ML%22%5BAuthor%5D>, *Laughlin NK* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22Laughlin+NK%22%5BAuthor%5D>, * DR* <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed & cmd=Search & itool=pubmed\ _Abstract & term=%22+DR%22%5BAuthor%5D>. Environmental Toxicology, University of California, Santa Cruz, California, USA. Although succimer (Chemet, meso-2,3-dimercaptosuccinic acid, DMSA) is considered to be a safe and effective chelating agent for the treatment of lead poisoning in humans, there is concern that it may increase the gastrointestinal (GI) absorption and retention of Pb from exposures suffered concurrent with treatment. This concern is justified because the availability of Pb-safe housing during outpatient treatment with oral succimer is limited. We used a juvenile nonhuman primate model of moderate childhood Pb intoxication and a sensitive double stable Pb isotope tracer methodology to determine whether oral succimer chelation affects the GI absorption and whole-body retention of Pb. Infant rhesus monkeys (n = 17) were exposed to Pb daily for 1 year postpartum to reach and maintain a target blood lead (BPb) level of 35-40 microg/dL. Animals were administered succimer (n = 9) or vehicle (n = 8) over two successive 19 day succimer treatment regimens beginning at 53 and 65 weeks of age. The present study was conducted over the second chelation regimen only. Animals received a single intravenous (iv) dose of stable (204)Pb tracer (5 microg, 24.5 nmol) followed by a single oral dose of stable (206)Pb tracer (72.6 microg, 352 nmol) immediately before chelation, in order to specifically evaluate GI Pb absorption and whole-body Pb retention with treatment. We collected complete urine and fecal samples over the first 5 days and whole blood over the first 8 days of treatment for analyses of stable Pb isotopes using magnetic sector inductively-coupled plasma mass spectrometry. Results indicate that succimer significantly reduced the GI absorption of Pb (vehicle, 64.9% +/- 5.5; succimer, 37.0% +/- 5.8; mean +/- SEM). Succimer also significantly increased the urinary excretion of endogenous Pb by approximately 4-fold over the vehicle treatment, while endogenous fecal Pb excretion was decreased by approximately 33%. Finally, although succimer reduced the whole-body retention of endogenous Pb by approximately 10% compared to vehicle, the majority (77%) of the administered internal dose of Pb tracer was retained in the body when assessed after 5 days of treatment. These data do not support the concern that succimer treatment increases GI Pb absorption. PMID: 11445516 boomerone2004 wrote: >I thought a while back you posted an abstract on lead poisoning and >it's effects on the GI system but of course now I can't find it after >I mentioned it to our doc. > >If you have any articles mentioning a connection I would appreciate it. > >Thanks, >Marie > > > > > > >Many frequently asked questions and answers can be found at <http://forums.autism-rxguidebook.com/default.aspx> > > Quote Link to comment Share on other sites More sharing options...
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