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From: Charly Coughran on 10 Sep 2008 13:03 admin(a)ng2000.com wrote in news:533793233634744.Post(a)ithinknot.net: > > http://www.ng2000.com/fw.php?tp=diabetes > > Washington, Sept 10 : While diabetes can make the beautifully > stratified retina look like over-fried bacon, scientists are > claiming that a drug, called pentazocine, known for its > pain-relieving power can prevent the retinal damage that leads to > vision loss. The site above is a list of current items which has apparently changed since the OP was there. The paper can be found at: http://www.iovs.org/cgi/content/full/49/9/4154 Super short abstract: mouse study. Full abstract: PURPOSE. To evaluate the neuroprotective properties of the sigma receptor 1 ({sigma}R1) ligand, (+)-pentazocine in an in vivo model of retinal neurodegeneration. METHODS. Spontaneously diabetic Ins2Akita/+ and wild-type mice received intraperitoneal injections of (+)-pentazocine for 22 weeks beginning at diabetes onset. Retinal mRNA and protein were analyzed by RT-PCR and Western blot analysis. Retinal histologic sections were measured to determine total retinal thickness, thicknesses of inner�outer nuclear and plexiform layers (INL, ONL, IPL, INL), and the number of cell bodies in the ganglion cell layer (GCL). Immunolabeling experiments were performed using antibodies specific for 4- hydroxynonenal and nitrotyrosine, markers of lipid peroxidation, and reactive nitrogen species, respectively, and an antibody specific for vimentin to view radial M�ller fibers. RESULTS. {sigma}R1 mRNA and protein levels in the Ins2Akita/+ retina were comparable to those in the wild-type, indicating that {sigma}R1 is an available target during the disease process. Histologic evaluation of eyes of Ins2Akita/+ mice showed disruption of retinal architecture. By 17 to 25 weeks after birth, Ins2Akita/+ mice demonstrated ~30% and 25% decreases in IPL and INL thicknesses, respectively, and a 30% reduction in ganglion cells. In the (+)- pentazocine-treated group, retinas of Ins2Akita/+ mice showed remarkable preservation of retinal architecture; IPL and INL thicknesses of (+)-pentazocine-treated Ins2Akita/+ mouse retinas were within normal limits. The number of ganglion cells was 15.6 � 1.5 versus 10.4 � 1.2 cells/100 �m retinal length in (+)-pentazocine- treated versus nontreated mutant mice. Levels of nitrotyrosine and 4- hydroxynonenal increased in Ins2Akita/+ retinas, but were reduced in (+)-pentazocine-treated mice. Retinas of Ins2Akita/+ mice showed loss of the uniform organization of radial M�ller fibers. Retinas of (+)- pentazocine-treated mice maintained the radial organization of glial processes. CONCLUSION. Sustained (+)-pentazocine treatment in an in vivo model of retinal degeneration conferred significant neuroprotection, reduced evidence of oxidative stress, and preserved retinal architecture, suggesting that {sigma}R1 ligands are promising therapeutic agents for intervention in neurodegenerative diseases of the retina. -- ------- Charly Coughran ccoughran(a)DELETE-TO-RESPOND-UCSD.EDU
From: dorsy1943 on 16 Sep 2008 07:22 On Sep 10, 1:03 pm, Charly Coughran <ccough...(a)REMOVE-TO-DELETE- UCSD.EDU> wrote: > ad...(a)ng2000.com wrote innews:533793233634744.Post(a)ithinknot.net: > > > > >http://www.ng2000.com/fw.php?tp=diabetes > > > Washington, Sept 10 : While diabetes can make the beautifully > > stratified retina look like over-fried bacon, scientists are > > claiming that a drug, called pentazocine, known for its > > pain-relieving power can prevent the retinal damage that leads to > > vision loss. > > The site above is a list of current items which has apparently changed > since the OP was there. The paper can be found at: > > http://www.iovs.org/cgi/content/full/49/9/4154 > > Super short abstract: mouse study. > > Full abstract: > > PURPOSE. To evaluate the neuroprotective properties of the sigma > receptor 1 ({sigma}R1) ligand, (+)-pentazocine in an in vivo model of > retinal neurodegeneration. > > METHODS. Spontaneously diabetic Ins2Akita/+ and wild-type mice > received intraperitoneal injections of (+)-pentazocine for 22 weeks > beginning at diabetes onset. Retinal mRNA and protein were analyzed by > RT-PCR and Western blot analysis. Retinal histologic sections were > measured to determine total retinal thickness, thicknesses of > innerouter nuclear and plexiform layers (INL, ONL, IPL, INL), and the > number of cell bodies in the ganglion cell layer (GCL). Immunolabeling > experiments were performed using antibodies specific for 4- > hydroxynonenal and nitrotyrosine, markers of lipid peroxidation, and > reactive nitrogen species, respectively, and an antibody specific for > vimentin to view radial Müller fibers. > > RESULTS. {sigma}R1 mRNA and protein levels in the Ins2Akita/+ retina > were comparable to those in the wild-type, indicating that {sigma}R1 > is an available target during the disease process. Histologic > evaluation of eyes of Ins2Akita/+ mice showed disruption of retinal > architecture. By 17 to 25 weeks after birth, Ins2Akita/+ mice > demonstrated ~30% and 25% decreases in IPL and INL thicknesses, > respectively, and a 30% reduction in ganglion cells. In the (+)- > pentazocine-treated group, retinas of Ins2Akita/+ mice showed > remarkable preservation of retinal architecture; IPL and INL > thicknesses of (+)-pentazocine-treated Ins2Akita/+ mouse retinas were > within normal limits. The number of ganglion cells was 15.6 ± 1.5 > versus 10.4 ± 1.2 cells/100 µm retinal length in (+)-pentazocine- > treated versus nontreated mutant mice. Levels of nitrotyrosine and 4- > hydroxynonenal increased in Ins2Akita/+ retinas, but were reduced in > (+)-pentazocine-treated mice. Retinas of Ins2Akita/+ mice showed loss > of the uniform organization of radial Müller fibers. Retinas of (+)- > pentazocine-treated mice maintained the radial organization of glial > processes. > > CONCLUSION. Sustained (+)-pentazocine treatment in an in vivo model of > retinal degeneration conferred significant neuroprotection, reduced > evidence of oxidative stress, and preserved retinal architecture, > suggesting that {sigma}R1 ligands are promising therapeutic agents for > intervention in neurodegenerative diseases of the retina. > > -- > ------- > Charly Coughran > ccough...(a)DELETE-TO-RESPOND-UCSD.EDU Charly, I have my retinas checked about twice a year and there are no problems so far, but I did develop posterior vitreous detachment over the past couple of years (flashing lights are a sign of the detachment and it is followed by floaters in the eye--very annoying--and this could eventually cause detachment of the retina.) The flashing lights and floaters could also be a sign of retinal detachment which is why I go twice a year to be checked. Do you know if the pvd is a complication of diabetes or due to other causes and it is just coincidental that I have diabetes. Thanks, Dolores
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