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Mayo Clinic

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PHYSIOCHEMICAL AND BIOLOGICAL PROPERTIES OF THE MAJOR BASIC PROTEIN FROM GUINEA PIG EOSINOPHIL GRANULES
Gleich, Gerald J. , Loegering, David A., Kueppers, Friedrich , Bajaj, Satya P., Mann, Kenneth G.

The Journal of Experimental Medicine | June 23, 2004 | Volume: 140 | Issue: 2 | Pages: 313-332

10.1084/jem.140.2.313 | PMID 4846413 Get It

Guinea pig eosinophil granules are characterized by the presence of a basic protein of low molecular weight which accounts for greater than 50% of granule protein. This protein, termed the major basic protein (MBP), readily aggregates and becomes insoluble, and the formation of aggregates is dependent on the establishment of disulfide bonds. Analysis of concentrated preparations of MBP often revealed a series of bands which were multiples of a monomeric unit with a mol wt of approximately 11,000. Analysis of reduced and alkylated MBP on a 10% agarose column equilibrated with 6 M guanidinium chloride revealed a single polypeptide chain with a mol wt of 10,800. Amino acid analysis of the protein revealed the presence of 13% arginine, consistent with the basic character of the molecule. Four residues of tryptophan, were present, indicating that MBP is not a histone. The MBP did not increase vascular permeability when injected into the skin of guinea pigs, nor did it antagonize the effect of histamine and bradykinin in the skin. MBP also did not contract the isolated guinea pig ileum and when mixed with histamine or bradykinin did not inhibit their activity on the gut. MBP had only weak, if any, antihistaminic activity. MBP possessed weak bactericidal activity when compared to histone and then only with one strain of E. coli. MBP precipitated DNA, neutralized heparin, and activated papain. On a molar basis MBP was more active than cysteine in activating papain. These results do not point to any unique biological activity associated with MBP other than those expected of a protein as basic as it is and one which possesses reactive sulfhydryl groups. Possible functions of eosinophils based on the properties of the MBP are discussed.
Assessing Sexual Behavior in High-Risk Adolescents with the Adolescent Clinical Sexual Behavior Inventory (ACSBI)
Friedrich, William N., Lysne, Marit, Sim, Leslie , Shamos, Susan

Child Maltreatment | June 22, 2004 | Volume: 9 | Issue: 3 | Pages: 239-250

10.1177/1077559504266907 | PMID 15245677 Get It

This study examined the reliability and validity of the Adolescent Clinical Sexual Behavior Inventory (ACSBI), a new 45-item measure, designed to elicit parent-and self-report regarding a range of sexual behaviors in high-risk adolescents. Using this measure, this study also investigated predictors of adolescent sexual behavior. Participants were 174 adolescents and their parents consecutively admitted to one of three clinical settings (i.e., inpatient treatment, partial hospital program, and outpatient clinic). Parent-and self-reports of adolescent sexual behavior were moderately correlated, and there was a strong relationship between high-risk sexual behavior and adolescent emotional and behavioral problems, as well as sexual concerns, distress, and preoccupation. In addition to sexual abuse, physical abuse, life stress, and impaired family relationships also significantly predicted sexual behavior in adolescents.
Gene Therapy for Thyroid Cancer: Current Status and Future Prospects
Spitzweg, Christine , Morris, John C.

Thyroid | June 22, 2004 | Volume: 14 | Issue: 6 | Pages: 424-434

10.1089/105072504323150732 | PMID 15242569 Get It

Metabolic Acidosis Associated with Propofol in the Absence of Other Causative Factors
Burow, Bethanie K., Packer, Douglas L. , Johnson, Michael E.

Anesthesiology | June 22, 2004 | Volume: 101 | Issue: 1 | Pages: 239-241

10.1097/00000542-200407000-00035 | PMID 15220796 Get It

Combination of Isoflurane and Caspase Inhibition Reduces Cerebral Injury in Rats Subjected to Focal Cerebral Ischemia
Inoue, Satoki , Drummond, John C., Davis, Daniel P. , Cole, Daniel J. , Patel, Piyush M.

Anesthesiology | June 22, 2004 | Volume: 101 | Issue: 1 | Pages: 75-81

10.1097/00000542-200407000-00013 | PMID 15220774 Get It

Background Recent data indicate that the neuroprotective efficacy of isoflurane is not sustained. Delayed neuronal death, mediated in part by apoptosis, contributes to the gradual increase in the size of the infarction. These data suggest that isoflurane may not be able to inhibit delayed neuronal death. The prevention of apoptosis by a caspase inhibitor might provide neuroprotection in addition to that provided by isoflurane. The current study was conducted to determine whether isoflurane-mediated neuroprotection can be made more durable with the administration of z-VAD-fmk, a nonspecific caspase inhibitor. Methods Fasted Wister rats were allocated to awake-zVAD, awake-vehicle, isoflurane-zVAD, or isoflurane-vehicle groups (n = 16/group). Animals were subjected to focal ischemia for 60 min by filament occlusion of the middle cerebral artery. In the awake groups, isoflurane was discontinued after occlusion of the middle cerebral artery. In the isoflurane groups, isoflurane anesthesia was maintained at 1.5 minimum alveolar concentration during occlusion of the middle cerebral artery. Before and after ischemia, daily injections of z-VAD-fmk or vehicle were administered into the lateral cerebral ventricle for 14 days. Neurologic assessment was performed 14 days after ischemia. The volume of cerebral infarction and the number of intact neurons in the periinfarct cortex were determined by image analysis of hematoxylin and eosin-stained coronal brain sections. Results Infarction volume was less in the isoflurane-zVAD group (23 +/- 11 mm, mean +/- SD) than in isoflurane-vehicle, awake-vehicle, and awake-zVAD groups (82 +/- 31, 86 +/- 31, and 59 +/- 25 mm, respectively; P < 0.05). In comparison with the awake-vehicle and isoflurane-vehicle groups, the administration of z-VAD-fmk significantly decreased infarction volume (P < 0.05). The infarction volume between the awake-vehicle and isoflurane-vehicle groups was not different. The number of intact neurons within the periinfarct cortex was significantly less in the awake-vehicle group than in the other three groups (P < 0.05). The isoflurane-zVAD group demonstrated better neurologic function than the awake-vehicle group (P < 0.05). Conclusion These findings are consistent with the premise that ongoing delayed neuronal death, in part mediated by apoptosis, contributes to the progression of cerebral infarction during the recovery period, and its inhibition can provide sustained neuroprotection.
Chemotherapy With or Without Radiotherapy in Limited-Stage Diffuse Aggressive Non-Hodgkin's Lymphoma: Eastern Cooperative Oncology Group Study 1484
Horning, Sandra J., Weller, Edie, Kim, KyungMann, Earle, John D., Glick, John H., O’Connell, Michael J. , Habermann, Thomas M.

Journal of Clinical Oncology | June 22, 2004 | Volume: 22 | Issue: 15 | Pages: 3032-3038

10.1200/jco.2004.06.088 | PMID 15210738 Get It

Purpose To compare low-dose (30 Gy) radiotherapy (RT) with observation (OBS) in limited-stage aggressive lymphoma patients achieving complete remission (CR) after chemotherapy, and to measure conversion from partial response (PR) to CR with high-dose (40 Gy) RT. Patients and Methods From 1984 to 1992, stage I (with risk factors) and II adults with diffuse aggressive lymphoma in CR after eight cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) were randomly assigned to 30 Gy involved-field RT or OBS. PR patients received 40 Gy RT. Results Among 172 CR patients, the 6-year disease-free survival (DFS) was 73% for low-dose RT versus 56% for OBS (two-sided P = .05). Failure-free survival (two-sided P = .06), and time to progression (two-sided P = .06) also favored RT. Intent-to-treat analyses yielded similar results. No survival differences were observed. Three RT versus 15 OBS patients relapsed in initial disease sites. At 6 years, failure-free survival was 63% in PR patients; conversion to CR did not significantly influence clinical outcome. Conclusion For patients in CR after CHOP, low-dose RT prolonged DFS and provided local control, but no survival benefit was observed. The majority of PR patients were event-free at 6 years despite residual radiographic abnormalities. Future efforts should be directed toward improved imaging and more effective systemic therapies.
Substitution of Oral Fluoropyrimidines for Infusional Fluorouracil With Radiotherapy: How Much Data Do We Need?
Crane, Christopher H. , Sargent, Daniel J. , Sargent, Daniel J

Journal of Clinical Oncology | June 22, 2004 | Volume: 22 | Issue: 15 | Pages: 2978-2981

10.1200/jco.2004.04.953 | PMID 15210736 Get It

Rhabdomyosarcoma Arising in the Hand or Foot: A Clinicopathologic Analysis
Miller, Dylan V. , Coffin, Cheryl M., Zhou, Holly

Pediatric and Developmental Pathology | June 19, 2004 | Volume: 7 | Issue: 4 | Pages: 361-369

10.1007/s10024-003-6071-1 | PMID 15383931 Get It

Rhabdomyosarcomas (RMS) arising at different anatomic sites have distinct clinicopathologic features that affect prognosis and outcome. RMS arising in the extremities generally have a worse prognosis. Case reports and anecdotal experience suggests the possibility that RMS of the hand or foot (RMSHF) may behave even more aggressively than RMS elsewhere in the extremities. This study describes clinicopathologic features and outcome of RMSHF. Charts and pathologic material from RMSHF cases from institutional files over a 32-year interval were reviewed. Additional cases from published reports and series over a 42-year interval were identified by a MEDLINE search. Pertinent clinicopathologic features for each case were compiled. Survival analysis and other data from these patients were compared with previously reported statistics in the literature for RMS at other anatomic sites, including elsewhere in the extremities. Six patients from the institutional files and 46 from published reports were identified. A number of adverse prognostic indicators were observed in the majority of these patients including alveolar morphology (86%) and distant metastasis at presentation (63%). Despite the aggressive nature of these tumors, the majority were smaller than 5 cm (61%). A propensity was observed for metastases to unusual sites such as breast, ovary, testis, pancreas, and kidney. The median survival was 19 months, and the 5-year survival was 27%. While these may reflect a constellation of findings related to site, it is also possible that alveolar histology is the main influence. RMSHF can present as a very small primary tumor with clinically evident or occult metastatic disease. Whether this reflects the location, the predominantly alveolar histologic type, or a molecular genetic subtype will require further analysis. Patients presenting with RMSHF should be thoroughly evaluated for occult metastases at the time of diagnosis and followed closely throughout treatment for subsequent involvement of unusual sites.
A genetic basis for the “Adonis” phenotype of low adiposity and strong bones
Johnson, Geoffrey B. , Riggs, B. Lawrence, Platt, Jeffrey L. , Johnson, Geoffrey B. , Johnson, Geoffrey B , Johnson, Geoffrey B

The FASEB Journal | June 18, 2004 | Volume: 18 | Issue: 11 | Pages: 1282-1284

10.1096/fj.04-1572fje | PMID 15208271 Get It

ABSTRACT Toll receptors in Drosophila contribute to host defense and establish the body plan. Mammalian homologues of Toll, the Toll‐like receptors (TLRs), are thought to function only in host defense. Here, we report that mice harboring mutations in TLR4 or in CD14, a co‐receptor for TLR4, have an “ideal” body plan consisting of increased bone mineral content, density, and size as well as decreased body fat. These mutant mice live long lives, have normal activity and fertility, and show no evidence of infection. Unlike many strains of caged wild‐type mice, they do not become obese. Although all mice continue to gain body fat, bone content, and overall weight, the difference in bone content and body fat between mutant and wild‐type mice increases with age. Thus, defects in TLR4/CD14 complex generate an “Adonis” phenotype, characterized by this ideal body type, and this function could potentially be exploited for the treatment of osteoporosis and obesity.
STUDIES IN EXPERIMENTAL EXTRACORPOREAL THROMBOSIS
Johnson, Walter R., Shionoya, Takuji, Rowntree, Leonard G.

Journal of Experimental Medicine | June 18, 2004 | Volume: 48 | Issue: 6 | Pages: 871-884

10.1084/jem.48.6.871 | PMID 19869528 Get It

In experimental obstructive jaundice in rabbits, thrombosis is definitely delayed in the extracorporeal loop. White thrombi are laid down at the normal rate in many instances; in others there is a delay in deposition of platelets, while in still others cauliflower-like masses of platelets are rapidly deposited and tend to slow or even stop the blood stream before much fibrin is apparent. Fibrin deposits and formation of the red thrombus usually appear late in the experiment and often only at the ends of the collodion tubes. In vigorous animals, the thrombi rarely tend to obstruct and usually cease growing when they have made up the difference between the lumen of the glass tube and of the collodion tube. On the other hand, if the animal's general condition is poor and its circulation depressed, red thrombus forms more rapidly and tends to encroach progressively on the lumen until obstruction takes place. Even in such cases circulation through the loop persists for periods much longer than in the normal animal. Judging from the gross appearance of the thrombus the quantity and quality of fibrin seem deficient. Single injections of bile salts yield pictures similar to those seen in experimental obstructive jaundice. White thrombi are deposited but obstruction of the lumen is delayed because of inadequate formation of fibrin. The continuous intravenous injection of bile salts resulted in a progressive increase of the clotting time and in the level of bile acids of the blood. The state of the extracorporeal loop was likewise similar in many respects to that seen in obstructive jaundice. There was, however, a definite decrease in the size and numbers of white thrombi deposited on the collodion membrane. From the evidence presented it is obvious that the processes of blood coagulation and of thrombosis in the extracorporeal loop are definitely delayed in experimental obstructive jaundice and in animals that have received intravenous injections of bile salts. No attempt is made to explain the changes found in jaundice on the basis of the increased levels of bile acids in the blood although these experiments would indicate that such a possibility has not been ruled out.