Thomas A. Ban
Neuropsychopharmacology in Historical Perspective
Education in the Field in the Post-Neuropsychopharmacology Era
Background to An Oral History of the First Fifty Years

Special Areas (Volume Seven): 5c. Contributions of Interviewees

(Bulletin 65)

 

           Three of the interviewees (Cooper, Dahl and Glassman) from Volume Seven were engaged in pharmacokinetic research (Ban 2011; Blackwell 2011).Thomas B. Cooper contributed to the determination of plasma and tissue levels of various antipsychotics (including butaperazine,, loxapine, clozapine and fluphenazine), antidepressants (including mianserin and nortriptyline) and benzodiazepines (Cooper 1989, 1996; Cooper, Simpson, Haher et al. 1975; Katz, Simpson, Jethanandi et al. 1989; Koreen, Lieberman, Alvir et al. 1994; Simpson, Cooper and Lee 1978; Suckow, Cooper, Quitkin and Steward 1982). In 1973, in collaboration with Bergner and Simpson, Cooper demonstrated that a 24-hour serum lithium level is a good “prognosticator” of dose requirement in patients (Cooper, Bergner and Simpson 1973). Cooper was member of the team which reported in 1980 on the effect of antiparkinsonian medication on plasma levels of chlorpromazine (Simpson, Cooper, Cooper, Bark et al. 1980). He was also a member of the team that compared (in 2004) the pharmacodynamic and pharmacokinetic effects of d and d,l-threo-methylphenidate hydrochloride in children with attention deficit disorder (Quinn, Wigal, Swanson et al. 2004).

            While studying the relationship between plasma levels and therapeutic effect of imipramine, in the 1970s, Alexander H. Glassman and his associates found that patients with delusions (psychotic depression) did not respond to the drug (Glassman, Hurrik and Perel 1972; Glassman, Kantor and Shostak 1975; Glassman, Perel, Shostak et al. 1977; Perel, Stiller and Glassman 1978). They also revealed cardiac conductance changes with imipramine, similar to those seen with quinidine (Kantor, Biger, Glassman et al. 1978; Kantor, Glassman, Biger et al. 1978). During the 1980s the focus of Glassman’s research shifted to smoking. He was among the first to demonstrate that clonidine, an α-2 adrenergic agonist, reduced the severity of symptoms after “smoking cessation.” He had also shown the effects of smoking cessation on major depression.

            Svein G. Dahl was among the first in the mid-1970s to study the pharmacokinetics of chlorpromazine and methotrimeprazine after the administration of single and multiple doses (Dahl 1986; Dahl and Straandjord 1977). Ten years later, in the mid-1980s, he was again among the first to introduce plasma level monitoring of antipsychotic drugs (Dahl 1986). During the 1990s the focus of Dahl’s research shifted to the study of structure-activity relationships and to the modeling of neurotransmitter receptors (Dahl, Edwardsen and Sylte 1991; Dahl, Kollman, Ran and Singh 1992).

            Two of the interviewees (George and Lisanby) were involved in research with biophysical approaches to treatment. Mark S. George was first in the 1990s to employ transcranial magnetic stimulation in the treatment of depression (George, Nahas, Kozel et al. 1999; George, Wasserman, Kimbrell et al. 1997; George, Wasserman, Williams et al. 1995). He was also first to explore the utility of vagus nerve stimulation in the treatment of psychiatric disorders (George, Rush, Sackeim et al. 2003).

In the early years of the 21st century Sarah Hollingsworth Lisanby was instrumental in developing magnetic seizure therapy and repetitive transcranial magnetic stimulationin the treatment of depression (Lisanby, Lubeck, Finck et al. 2000; Lisanby, Lubeck, Schlaepfer and Sackeim 2003; Lisanby, Morales. Payne et al. 2003; Lisanby, Schlaepfer and Fisch 2001).  She also explored the possible augmentation of sertraline treatment with transcranial magnetic stimulation (Lisanby, Pascal-Leone, Sampson et al. 2001).  

Each of the remaining six interviewees (Arango, Costa, Kupfer, McKinney, Shooter and Weissman) was involved in a different are of research. Victoria Arango with her associates demonstrated an increase in serotonin 5HT2 and β-adrenergic receptor binding sites in the brains of suicide victims in the 1990s (Arango, Ernsberger, Maszuk et al. 1990). They localized the increase of serotonin receptor binding sites to the ventrolateral prefrontal cortex (Arango, Underwood, Gubbi et al. 1995). In 2002 Arrango was member of the team which reported on altered editing of serotonin 5HT2c receptor pre-mRNA in the prefrontal cortex in suicide and in 2006 she was member of the team that demonstrated lower serotonin transporter binding during major depressive episode (Gurevich, Tamur, Arango et al. 2002; Parsey, Hastings, Oquendo et al. 2006).

            Erminio Costa was first to demonstrate the differential expression of serotonin in various areas of the human brain in the late 1950s (Costa and Aprison 1958). His findings indicated multiple serotonin receptors with different sensitivity to inhibition by lysergic acid diethylamide (LSD) (Costa 1960, 2003). In the 1970s Costa and his associates demonstrated that potentiation of gabaminergic activity plays an important role in the mode of action of benzodiazepines (Costa, Guidotti, Mao and Suria 1975; Guidotti, Baraldi and Costa 1979). They also contributed to the characterization of benzodiazepine receptors (Guidotti, Toffano and Costa 1978). In the mid-1980s Costa was member of the team that discovered metabotropic glutamate receptors (Nicoletti, Meek, Iadarola et al. 1985). In the early years of the 21st century Costa and his associates found that reelin protein and mRNA was reduced in several brain areas in schizophrenia and manic-depressive disease and suggested that dendritic spine hypoplasticity with downregulation of reelin and GABAergic tone is a vulnerability factor for schizophrenia (Costa, Davis, Grayson et al. 2001). In 2002 they postulated that schizophrenia is a disease at the interface of the genome and the epigenome (Costa, Chen, Davis et al. 2002).   

             In the 1970s David J Kupfer reported on changed interval between the onset of sleep and rapid eye-movement sleep in depressed patients and suggested that shortened rapid eye movement (REM) latency was an indicator (“biological marker”) of primary depressive disease (Kupfer 1976; Kupfer and Foster 1972). Kupfer found a statistically significant relationship between the changes in the tonic component of REM sleep and therapeutic response to antidepressants. He also demonstrated that an increase in REM latency and REM suppression after a loading dose of 50 mg of amitriptyline was a predictor of favorable treatment outcome with the drug (Kupfer, Harris, Spiker et al. 1978, 1979).In other areas of research Kupfer contributed to knowledge on maintenance treatment in recurrent depression and on the management of insomnia (Kupfer, Frank, Perel et al. 1992; Kupfer and Reynolds 1997). 

Working with rhesus monkeys William T. McKinney was first in the 1970s to report on the effect of reserpine on social behaviour and on the effect of chlorpromazine on disturbed behavior (McKinney, Eising, Moran et al. 1972; McKinney, Young, Suomi and Davis 1873). In the 1980s he studied the effects of several drugs on the response to social isolation and published his monograph “Animal Models of Mental Disorders” (McKinney 1988; McKinney, Moran and Kraemer 1983).

            In 1976 Eric M. Shooter, in collaboration with Mobley and Schenker, succeeded with the isolation and characterization of “proteolytically modified nerve growth factor” (Mobley, Schenker and Shooter1976). Twenty-six years later, in 2002, Shooter, in collaboration with Cosgaya and Chan, reported that the neurotrophin receptor p75NTR is a positive modulator of myelinisation (Cosgaya, Chan and Shooter 2002).

            Myrna M Weissman was among the first to use psychiatric research diagnostic criteria in epidemiological studies (Weissman and Klerman 1978). In the late 1970s she published her findings on affective disorder in an urban community of the United States and in 1980 she presented epidemiological findings on depression in New Haven (Klerman, DiMascio, Weissman et al. 1974; Weissman and Myers 1980). During the 1970s and ‘80s, Weissman, in collaboration with Gerald Klerman, studied the interaction between drugs and psychotherapy in the treatment of depression and developed short-term interpersonal psychotherapy. Subsequently, she became involved in molecular genetic research in psychiatry (Hamilton, Fyer, Durner et al. 2003; Holmans, Weissman, Zubenko et al. 2007; Klerman, Weissman, Rounsaville and Chevron 1984; Weissman, Pilowsky, Wickramaratne 2006; Weissman, Wickramaratne, Nomura et al. 2006).

The background of interviewees in Volume Seven varies widely. Their only common feature is that all 29 interviewees are members of ACNP.

Interviewees entered the field at different stages in the development of neuropsychopharmacology. Hence the volume covers 50 years of history.

 

References:

 

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Arango V, Underwood MD, Gubbi AV, Mann JJ. Localized alterations in pre- and postsynaptic serotonin binding sites in the ventrolateral prefrontal cortex of suicide victims. Brain Res 1995; 688: 121-3.

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Guidotti A, Baraldi M, Costa E. 1,4 Benzodiazepines and γ-aminobutyric acid: pharmacological and biochemical correlates.  Pharmacology 1979 19; 267-77.

Guidotti A, Toffano G, Costa E. An endogenous protein modulates the affinity of GABA and benzodiazepin receptors in rat brain.  Nature 1978; 257: 553-5.

Gurevich I, Tamir H, Arango V, Mann JJ, Dwork AJ, Schmauss C. Altered editing of serotonin HT2c receptor pre-mRNA in the prefrontal cortex of depressed suicide victims. Neuron 2002; 34: 349-56.

Hamilton SP, Fyer AJ, Durner M, Heiman GA, deLeon AB, Hodge SE, Knowles JA, Weissman MM. Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q.  Proc Nat Acad Sciences  2003; 100: 2550-5.

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Nicoletti  F, Meek JL, Iadarola  MJ, Chuang DM, Roth BL, Costa E. Coupling of inositol  phospholipid metabolism with excitatory amino acid  recognition sites  in rat hippocampus. J Neurochem 1985; 46:40-5. 

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Simpson GM, Cooper TB, Lee JH, Young MA. Clinical and plasma level characterization of intramascular and oral loxapine. Psychopharmacology 1978; 58: 225-32. 

Suckow RF, Cooper TB, Quitkin FM, Steward JW. Determination of mianserin and metabolites in plasma by liquid chromatography with electrochemical detector. Journal of Pharmaceutical Sciences 1982; 71: 889-92.

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Weissman MM, Wickramaratne P, NomuraY, Warner V, Pilowsky D, Verdeli H. Offspring of depressed parents: 20 years later. Am J Psychiatry   2006; 163: 1001-8.

 

April 11, 2019