Abstract
After a primary infection with 100 Angiostrongylus cantonensis larvae, infected rats showed elevated phospholipase B activity in meningeal and brain homogenates beginning with the first week and continuing through the first month of infection. The rise in phospholipase B values through the first 4 weeks, with a prolonged peak spanning days 30 to 31, coincided with the invasion and maturation of the parasites in the brain, and the ensuing sharp decline in phospholipase B levels, shown by the readings on day 45, coincided in turn with the known migration of the worms from the brain to the lungs, which begins about 5 weeks after infection. In the meninges, the pattern of enzyme elevation was generally similar to that in the brain samples except that the highest activity was seen earlier at days 8 to 9, followed by a gradual decline by days 30 to 31 and a sharper drop by day 45. Rats challenged with 100 larvae 53 days after the primary infection exhibited an almost immediate rise of phospholipase B activity in both the brain and meninges; the peaks of activity occurred at day 1 for the meninges and day 25 for the brain, and levels above control values were still present at day 50. Comparison of the total enzymatic content of the cerebral tissue and meninges revealed that a remarkably high proportion of the phospholipase B activity was contained in the meninges. The inference that elevated levels of this enzyme in the cerebral tissue of A. cantonensis-infected rats are due to inflammatory reactions within the meningeal envelopes was confirmed by histochemical demonstration of specific sites of enzymatic activity limited to the meninges. It is of interest that 80% of the cells positive for the enzyme were clearly identifiable as eosinophils since an association of bone marrow eosinophilia and high phospholipase B levels in rats infected with A. cantonensis was shown in our earlier study of rats infected with this parasite.
Full text
PDF








Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Basten A., Beeson P. B. Mechanism of eosinophilia. II. Role of the lymphocyte. J Exp Med. 1970 Jun 1;131(6):1288–1305. doi: 10.1084/jem.131.6.1288. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Basten A., Boyer M. H., Beeson P. B. Mechanism of eosinophilia. I. Factors affecting the eosinophil response of rats to Trichinella spiralis. J Exp Med. 1970 Jun 1;131(6):1271–1287. doi: 10.1084/jem.131.6.1271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butterworth A. E., David J. R., Franks D., Mahmoud A. A., David P. H., Sturrock R. F., Houba V. Antibody-dependent eosinophil-mediated damage to 51Cr-labeled schistosomula of Schistosoma mansoni: damage by purieid eosinophils. J Exp Med. 1977 Jan 1;145(1):136–150. doi: 10.1084/jem.145.1.136. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butterworth A. E., Sturrock R. F., Houba V., Mahmoud A. A., Sher A., Rees P. H. Eosinophils as mediators of antibody-dependent damage to schistosomula. Nature. 1975 Aug 28;256(5520):727–729. doi: 10.1038/256727a0. [DOI] [PubMed] [Google Scholar]
- DOLE V. P. A relation between non-esterified fatty acids in plasma and the metabolism of glucose. J Clin Invest. 1956 Feb;35(2):150–154. doi: 10.1172/JCI103259. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grove D. I., Mahmoud A. A., Warren K. S. Eosinophils and resistance to Trichinella spiralis. J Exp Med. 1977 Mar 1;145(3):755–759. doi: 10.1084/jem.145.3.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jindrak K. Angiostrongyliasis cantonensis (eosinophilic meningitis, Alicata's disease). Contemp Neurol Ser. 1975;12:133–164. [PubMed] [Google Scholar]
- Jindrák K. Early migration and pathogenicity of Angiostrongylus cantonensis in laboratory rats. Ann Trop Med Parasitol. 1968 Dec;62(4):506–517. doi: 10.1080/00034983.1968.11686591. [DOI] [PubMed] [Google Scholar]
- Jindrák K. The pathology of intracranial angiostrongylosis in rats. J Comp Pathol. 1970 Apr;80(2):287–297. doi: 10.1016/0021-9975(70)90097-6. [DOI] [PubMed] [Google Scholar]
- Larsh J. E., Jr, Ottolenghi A., Weatherly N. F. Trichinella spiralis: phospholipase in challenged mice and rats. Exp Parasitol. 1974 Oct;36(2):299–306. doi: 10.1016/0014-4894(74)90069-1. [DOI] [PubMed] [Google Scholar]
- Larsh J. E., Jr Trichinella spiralis: phospholipase in sensitized mice after challenge. Exp Parasitol. 1975 Apr;37(2):233–238. doi: 10.1016/0014-4894(75)90075-2. [DOI] [PubMed] [Google Scholar]
- Ottolenghi A., Barnett H. D. The effect of drugs on the eosinophilic leukocyte population of rat tissues. I. Dexamethasone. J Pharmacol Exp Ther. 1974 May;189(2):303–311. [PubMed] [Google Scholar]
- Ottolenghi A., Kocan A. A., Weatherly N. F., Larsh J. E., Jr Nippostrongylus brasiliensis: phospholipase in nonsensitized and sensitized rats after challenge. Exp Parasitol. 1975 Aug;38(1):96–104. doi: 10.1016/0014-4894(75)90042-9. [DOI] [PubMed] [Google Scholar]
- Ottolenghi A. The relationship between eosinophilic leukocytes and phospholipase B activity in some rat tissues. Lipids. 1970 Jun;5(6):531–538. doi: 10.1007/BF02532741. [DOI] [PubMed] [Google Scholar]
- Ottolenghi A., Weatherly N. F., Kocan A. A., Larsh J. E., Jr Angiostrongylus cantonensis: phospholipase in nonsensitized and sensitized rats after challenge. Infect Immun. 1977 Jan;15(1):13–18. doi: 10.1128/iai.15.1.13-18.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ottolenghi A, Pickett J P, Greene W B. Histochemical demonstration of phospholipase B (lysolecithinase) activity in rat tissues. J Histochem Cytochem. 1966 Dec;14(12):907–914. doi: 10.1177/14.12.907. [DOI] [PubMed] [Google Scholar]
- Richards C. S., Merritt J. W. Studies on Angiostrongylus cantonensis in molluscan intermediate hosts. J Parasitol. 1967 Apr;53(2):382–388. [PubMed] [Google Scholar]


