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CMAJ January 17, 2006 174(2) | 152 News Neuroprotection after stroke Stroke is major cause of morbidity and death in the elderly population. Al- though a small proportion of patients who experience stroke arrive at hospital early enough for reperfusion therapy, for most patients the treatment options are limited. Neuronal death as a result of inflammation and apoptosis contin- ues after the initial ischemic insult. New research reveals a potential target that might help to limit neuronal death. A molecule called NF-κB is known to have antiapoptotic effects in non- neuronal cells. Oliver Herrmann and colleagues targeted an enzyme called IKK2 that regulates the activation of the NF-κB protein. The scientists created 2 strains of mice: one that lacked IKK2 in neurons and another in which IKK2 was always turned on in the same cells. They found that, after induced cerebral ischemia, mice lacking IKK2 had re- duced infarct size compared with mice in which IKK2 was activated (Nature Med 2005; doi:10.1038/nm1323). The results suggest that pharmaco- logic inhibition of IKK2 might be suc- cessful in the treatment of stroke. Sev- eral IKK2 inhibitors already exist. Herrmann and colleagues found that administration of a known IKK2 in- hibitor after cerebral ischemia in mice reduced the volume of cell death by 60%. This effect worked for up to 4.5 hours after the stroke, which may bode well for human patients who require time to reach a hospital. have received attention over the years as potential antiseptics, spasmolytics, di- uretics and antidepressants. To determine its antiviral properties, the authors extracted p27 SJ from cul- tured cells of the St. John’s Wort plant and found that, in human cells infected with HIV-1, the extract suppressed the transcription of the viral genome. The scientists determined that p27 SJ is able to do this by interacting with 2 key proteins involved in HIV replication. When injected into microglial cells along with HIV-1, p27 SJ reduced viral replication by almost 50% (Gene Ther 2005; doi:10.1038/sj.gt.3302649). St. John’s Wort is widely available as an herbal supplement. Whether com- mercially available preparations con- tain p27 SJ is unclear, and their use as al- ternative therapy for HIV infection is not recommended. Rather, the find- ings should be interpreted as hypothe- sis generating. — Compiled by David Secko, Vancouver HIV stalled by St. John’s Wort St. John’s Wort, a widely used herbal remedy for depression, has been re- cently shown to contain a component that inhibits HIV replication. Although the findings are preliminary and the protein, named p27 SJ , is far from being recommended as a treatment for HIV infection, the findings suggest the pos- sibility of alternative therapeutic strate- gies for HIV infection. Nune Darbinian-Sarkissian and col- leagues recently discovered p27 SJ while looking at the effects of plant extracts from St. John’s Wort on the behaviour of brain cells in culture. Such extracts Bench to Bedside DOI:10.1503/cmaj.051539 Erowid.org Photos.com

Neuroprotection after stroke · 2006. 1. 6. · Neuroprotection after stroke Stroke is major cause of morbidity and death in the elderly population. Al-though a small proportion of

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Page 1: Neuroprotection after stroke · 2006. 1. 6. · Neuroprotection after stroke Stroke is major cause of morbidity and death in the elderly population. Al-though a small proportion of

CMAJ • January 17, 2006 • 174(2) | 152

News

Neuroprotection

after stroke

Stroke is major cause of morbidity anddeath in the elderly population. Al-though a small proportion of patientswho experience stroke arrive at hospitalearly enough for reperfusion therapy,for most patients the treatment optionsare limited. Neuronal death as a resultof inflammation and apoptosis contin-ues after the initial ischemic insult.New research reveals a potential targetthat might help to limit neuronal death.

A molecule called NF-κB is knownto have antiapoptotic effects in non-neuronal cells. Oliver Herrmann andcolleagues targeted an enzyme calledIKK2 that regulates the activation of theNF-κB protein. The scientists created 2strains of mice: one that lacked IKK2 inneurons and another in which IKK2was always turned on in the same cells.They found that, after induced cerebralischemia, mice lacking IKK2 had re-duced infarct size compared with micein which IKK2 was activated (NatureMed 2005; doi:10.1038/nm1323).

The results suggest that pharmaco-logic inhibition of IKK2 might be suc-cessful in the treatment of stroke. Sev-eral IKK2 inhibitors already exist.Herrmann and colleagues found thatadministration of a known IKK2 in-hibitor after cerebral ischemia in micereduced the volume of cell death by60%. This effect worked for up to 4.5hours after the stroke, which may bodewell for human patients who requiretime to reach a hospital.

have received attention over the years aspotential antiseptics, spasmolytics, di-uretics and antidepressants.

To determine its antiviral properties,the authors extracted p27SJ from cul-tured cells of the St. John’s Wort plantand found that, in human cells infectedwith HIV-1, the extract suppressed thetranscription of the viral genome. Thescientists determined that p27SJ is ableto do this by interacting with 2 keyproteins involved in HIV replication.When injected into microglial cellsalong with HIV-1, p27SJ reduced viralreplication by almost 50% (Gene Ther2005; doi:10.1038/sj.gt.3302649).

St. John’s Wort is widely available asan herbal supplement. Whether com-mercially available preparations con-tain p27SJ is unclear, and their use as al-ternative therapy for HIV infection isnot recommended. Rather, the find-ings should be interpreted as hypothe-sis generating. — Compiled by DavidSecko, Vancouver

HIV stalled

by St. John’s Wort

St. John’s Wort, a widely used herbalremedy for depression, has been re-cently shown to contain a componentthat inhibits HIV replication. Althoughthe findings are preliminary and theprotein, named p27SJ, is far from beingrecommended as a treatment for HIVinfection, the findings suggest the pos-sibility of alternative therapeutic strate-gies for HIV infection.

Nune Darbinian-Sarkissian and col-leagues recently discovered p27SJ whilelooking at the effects of plant extractsfrom St. John’s Wort on the behaviourof brain cells in culture. Such extracts

Bench to Bedside

DOI:10.1503/cmaj.051539

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