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1.
Instr Course Lect ; 50: 483-8, 2001.
Article in English | MEDLINE | ID: mdl-11372349

ABSTRACT

There are several options for the treatment of patients with osteonecrosis about the knee. Three appear to be the most effective and include conservative treatment for small lesions without evidence of structural collapse, core decompression for relief of pain and possible delay in structural collapse in the patients with steroid-induced osteonecrosis, and either unicompartmental or total knee arthroplasty. Although other modalities have been reported, these three remain the most widely reported and generally offer the greatest success. With better recognition of these problems, longer duration follow-up, and larger patient series, the answers to the best treatment regimen will become better defined.


Subject(s)
Knee Joint , Osteonecrosis/surgery , Adult , Arthroplasty , Debridement , Decompression, Surgical , Humans , Osteonecrosis/etiology , Osteotomy , Steroids/adverse effects
2.
Am J Physiol Gastrointest Liver Physiol ; 278(1): G148-55, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10644573

ABSTRACT

Recent investigations have suggested carbon monoxide (CO) as a putative messenger molecule. Although several studies have implicated the heme oxygenase (HO) pathway, responsible for the endogenous production of CO, in the neuromodulatory control of the internal anal sphincter (IAS), its exact role is not known. Nitric oxide, produced by neuronal nitric oxide synthase (nNOS) of myenteric neurons, is an important inhibitory neural messenger molecule mediating nonadrenergic noncholinergic (NANC) relaxation of the IAS. The present studies were undertaken to investigate in detail the presence and coexistence of heme oxygenase-2 (HO-2) with nNOS in the opossum anorectum. In perfusion-fixed, frozen-sectioned tissue, HO-2 immunoreactive (IR) and nNOS IR nerves were identified using immunocytochemistry. Ganglia containing HO-2 IR neuronal cell bodies were present in the myenteric and submucosal plexuses throughout the entire anorectum. Colocalization of HO-2 IR and nNOS IR was nearly 100% in the IAS and decreased proximally from the anal verge. In the rectum, colocalization of HO-2 IR and nNOS IR was approximately 70%. Additional confocal microscopy studies using c-Kit staining demonstrated the localization of HO-2 IR and nNOS IR in interstitial cells of Cajal (ICC) of the anorectum. From the high rate of colocalization of HO-2 IR and nNOS IR in the IAS as well as the localization of HO-2 IR and nNOS IR in ICC in conjunction with earlier studies of the HO pathway, we speculate an interaction between HO and NOS pathways in the NANC inhibitory neurotransmission of the IAS and rectum.


Subject(s)
Anal Canal/enzymology , Heme Oxygenase (Decyclizing)/metabolism , Nitric Oxide Synthase/metabolism , Rectum/enzymology , Anal Canal/innervation , Animals , Immunohistochemistry , In Vitro Techniques , Myenteric Plexus/enzymology , Nitric Oxide Synthase Type I , Opossums , Rectum/innervation , Submucous Plexus/enzymology , Tissue Distribution
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